Exercise benefits on Alzheimer’s disease: State-of-the-science

Macrophage plasticity and polarization: in vivo veritas

Sica, A., & Mantovani, A. (2012) · Journal of Clinical Investigation · doi:10.1172/jci59643 · Cited by 6,335 · see citing works

Neuroinflammation in Alzheimer's disease

Heneka, M. T., Carson, M. J., Khoury, J. E., Landreth, G. E., Brosseron, F., Feinstein, D. L., Jacobs, A. H., Wyss-Coray, T., Vitorica, J., Ransohoff, R. M., et al. (2015) · The Lancet Neurology · doi:10.1016/s1474-4422(15)70016-5 · Cited by 6,226 · see citing works

Exercise training increases size of hippocampus and improves memory

Erickson, K. I., Voss, M. W., Prakash, R. S., Basak, C., Szabo, A., Chaddock, L., Kim, J. S., Heo, S., Alves, H., White, S. M., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1015950108 · Cited by 4,855 · see citing works

Metabolic regulation of gene expression by histone lactylation

Zhang, D., Tang, Z., Huang, H., Zhou, G., Cui, C., Weng, Y., Liu, W., Kim, S., Lee, S., Perez-Neut, M., et al. (2019) · Nature · doi:10.1038/s41586-019-1678-1 · Cited by 4,371 · see citing works

Default-mode network activity distinguishes Alzheimer’s disease from healthy aging: evidence from functional MRI

Greicius, M. D., Srivastava, G., Reiss, A. L., & Menon, V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308627101 · Cited by 3,684 · see citing works

Exercise as medicine - evidence for prescribing exercise as therapy in 26 different chronic diseases

Pedersen, B. K., & Saltin, B. (2015) · Scandinavian Journal of Medicine & Science in Sports · doi:10.1111/sms.12581 · Cited by 3,514 · see citing works

Alzheimer’s Disease

Scheltens, P., Blennow, K., Breteler, M. M. B., de Strooper, B., Frisoni, G. B., Salloway, S., & Van der Flier, W. M. (2016) · The Lancet · doi:10.1016/s0140-6736(15)01124-1 · Cited by 3,125 · see citing works

Functional Polarization of Tumour-Associated Macrophages by Tumour-Derived Lactic Acid

Colegio, O. R., Chu, N.-Q., Szabo, A. L., Chu, T., Rhebergen, A. M., Jairam, V., Cyrus, N., Brokowski, C. E., Eisenbarth, S. C., Phillips, G. M., et al. (2014) · Nature · doi:10.1038/nature13490 · Cited by 3,046 · see citing works

NLRP3 is activated in Alzheimer’s disease and contributes to pathology in APP/PS1 mice

Heneka, M. T., Kummer, M. P., Stutz, A., Delekate, A., Schwartz, S., Vieira-Saecker, A., Griep, A., Axt, D., Remus, A., Tzeng, T.-C., et al. (2013) · Nature · doi:10.1038/nature11729 · Cited by 2,898 · see citing works

Lack of Exercise Is a Major Cause of Chronic Diseases

Booth, F. W., Roberts, C. K., & Laye, M. J. (2012) · Comprehensive Physiology · doi:10.1002/cphy.c110025 · Cited by 2,575 · see citing works

The NALP3 inflammasome is involved in the innate immune response to amyloid-β

Halle, A., Hornung, V., Petzold, G. C., Stewart, C. R., Monks, B. G., Reinheckel, T., Fitzgerald, K. A., Latz, E., Moore, K. J., & Golenbock, D. T. (2008) · Nature Immunology · doi:10.1038/ni.1636 · Cited by 2,441 · see citing works

Exercise builds brain health: key roles of growth factor cascades and inflammation

Cotman, C. W., Berchtold, N. C., & Christie, L.-A. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.06.011 · Cited by 2,268 · see citing works

Computational systems biology.

Kitano, H. (2002) · Nature · doi:10.1038/nature01254 · Cited by 2,209 · see citing works

The ketone metabolite β-hydroxybutyrate blocks NLRP3 inflammasome-mediated inflammatory disease

Youm, Y.-H., Nguyen, K. Y., Grant, R. W., Goldberg, E. L., Bodogai, M., Kim, D., D'Agostino, D., Planavsky, N., Lupfer, C., Kanneganti, T. D., et al. (2015) · Nature Medicine · doi:10.1038/nm.3804 · Cited by 2,172 · see citing works

Immune attack: the role of inflammation in Alzheimer disease

Heppner, F. L., Ransohoff, R. M., & Becher, B. (2015) · Nature Reviews Neuroscience · doi:10.1038/nrn3880 · Cited by 2,134 · see citing works

Microglia and macrophages in brain homeostasis and disease

Li, Q., & Barres, B. A. (2018) · Nature Reviews Immunology · doi:10.1038/nri.2017.125 · Cited by 1,999 · see citing works

Leisure Activities and the Risk of Dementia in the Elderly

Verghese, J., Lipton, R. B., Katz, M. J., Hall, C. B., Derby, C. A., Kuslansky, G., Ambrose, A. F., Sliwinski, M., & Buschke, H. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa022252 · Cited by 1,961 · see citing works

Oxidative Stress, Synaptic Dysfunction, and Alzheimer’s Disease

Tönnies, E., & Trushina, E. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-161088 · Cited by 1,750 · see citing works

Astrocyte-Neuron Lactate Transport Is Required for Long-Term Memory Formation

Suzuki, A., Stern, S. A., Bozdagi, O., Huntley, G. W., Walker, R. H., Magistretti, P. J., & Alberini, C. M. (2011) · Cell · doi:10.1016/j.cell.2011.02.018 · Cited by 1,711 · see citing works

A N <scp>EW</scp> A <scp>PPROACH TO</scp> D <scp>ECODING</scp> L <scp>IFE</scp> : Systems Biology

Ideker, T., Galitski, T., & Hood, L. (2001) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev.genom.2.1.343 · Cited by 1,664 · see citing works

A century of trends in adult human height

NCD Risk Factor Collaboration (NCD-RisC) (2016) · eLife · doi:10.7554/elife.13410 · Cited by 1,558 · see citing works

Exercise induces hippocampal BDNF through a PGC-1α/FNDC5 pathway

Wrann, C. D., White, J. P., Salogiannnis, J., Laznik-Bogoslavski, D., Wu, J., Ma, D., Lin, J. D., Greenberg, M. E., & Spiegelman, B. M. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.09.008 · Cited by 1,440 · see citing works

The dynamic functional connectome: State-of-the-art and perspectives

Preti, M. G., Bolton, T. A. W., & Ville, D. V. D. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.12.061 · Cited by 1,425 · see citing works

Kynurenines: Tryptophan’s metabolites in exercise, inflammation, and mental health

Cervenka, I., Agudelo, L. Z., & Ruas, J. L. (2017) · Science · doi:10.1126/science.aaf9794 · Cited by 1,382 · see citing works

Aerobic High-Intensity Intervals Improve V˙O2max More Than Moderate Training

HELGERUD, J., HØYDAL, K., WANG, E., KARLSEN, T., BERG, P., BJERKAAS, M., SIMONSEN, T., HELGESEN, C., HJORTH, N., BACH, R., et al. (2007) · Medicine &amp; Science in Sports &amp; Exercise · doi:10.1249/mss.0b013e3180304570 · Cited by 1,332 · see citing works

The effects of exercise training on elderly persons with cognitive impairment and dementia: A meta-analysis11No commercial party having a direct financial interest in the results of the research supporting this article has or will confer a benefit upon the author(s) or upon any organization with which the author(s) is/are associated.

Heyn, P., Abreu, B. C., & Ottenbacher, K. J. (2004) · Archives of Physical Medicine and Rehabilitation · doi:10.1016/j.apmr.2004.03.019 · Cited by 1,223 · see citing works

Physical activity and risk of cognitive decline: a meta-analysis of prospective studies

Sofi, F., Valecchi, D., Bacci, D., Abbate, R., Gensini, G. F., Casini, A., & Macchi, C. (2011) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2010.02281.x · Cited by 1,210 · see citing works

Midlife blood pressure and dementia: the Honolulu–Asia aging study☆

Launer, L. J., Ross, G. W., Petrovitch, H., Masaki, K., Foley, D., White, L. R., & Havlik, R. J. (2000) · Neurobiology of Aging · doi:10.1016/s0197-4580(00)00096-8 · Cited by 1,008 · see citing works

Exercise-linked FNDC5/irisin rescues synaptic plasticity and memory defects in Alzheimer’s models

Lourenco, M. V., Frozza, R. L., de Freitas, G. B., Zhang, H., Kincheski, G. C., Ribeiro, F. C., Gonçalves, R. A., Clarke, J. R., Beckman, D., Staniszewski, A., et al. (2019) · Nature Medicine · doi:10.1038/s41591-018-0275-4 · Cited by 935 · see citing works

Comparison between different D ‐ D imer cutoff values to assess the individual risk of recurrent venous thromboembolism: analysis of results obtained in the DULCIS study

Palareti, G., Legnani, C., Cosmi, B., Antonucci, E., Erba, N., Poli, D., Testa, S., Tosetto, A., & the DULCIS (D‐dimer‐ULtrasonography in Combination Italian Study) Investigators (See Appendix) (2015) · International Journal of Laboratory Hematology · doi:10.1111/ijlh.12426 · Cited by 921 · see citing works

Evidence for a release of brain-derived neurotrophic factor from the brain during exercise

Rasmussen, P., Brassard, P., Adser, H., Pedersen, M. V., Leick, L., Hart, E., Secher, N. H., Pedersen, B. K., & Pilegaard, H. (2009) · Experimental Physiology · doi:10.1113/expphysiol.2009.048512 · Cited by 914 · see citing works

Exercise promotes the expression of brain derived neurotrophic factor (BDNF) through the action of the ketone body β-hydroxybutyrate

Sleiman, S. F., Henry, J., Al-Haddad, R., El Hayek, L., Abou Haidar, E., Stringer, T., Ulja, D., Karuppagounder, S. S., Holson, E. B., Ratan, R. R., et al. (2016) · eLife · doi:10.7554/elife.15092 · Cited by 810 · see citing works

Exercise benefits in cardiovascular disease: beyond attenuation of traditional risk factors

Fiuza-Luces, C., Santos-Lozano, A., Joyner, M., Carrera-Bastos, P., Picazo, O., Zugaza, J. L., Izquierdo, M., Ruilope, L. M., & Lucia, A. (2018) · Nature Reviews Cardiology · doi:10.1038/s41569-018-0065-1 · Cited by 803 · see citing works

Combined adult neurogenesis and BDNF mimic exercise effects on cognition in an Alzheimer’s mouse model

Choi, S. H., Bylykbashi, E., Chatila, Z. K., Lee, S. W., Pulli, B., Clemenson, G. D., Kim, E., Rompala, A., Oram, M. K., Asselin, C., et al. (2018) · Science · doi:10.1126/science.aan8821 · Cited by 802 · see citing works

Oxidative stress in Alzheimer’s disease

Chen, Z., & Zhong, C. (2014) · Neuroscience Bulletin · doi:10.1007/s12264-013-1423-y · Cited by 797 · see citing works

Monocarboxylate transporters in the central nervous system: distribution, regulation and function

Pierre, K., & Pellerin, L. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03168.x · Cited by 744 · see citing works

Skeletal Muscle PGC-1α1 Modulates Kynurenine Metabolism and Mediates Resilience to Stress-Induced Depression

Agudelo, L. Z., Femenía, T., Orhan, F., Porsmyr-Palmertz, M., Goiny, M., Martinez-Redondo, V., Correia, J. C., Izadi, M., Bhat, M., Schuppe-Koistinen, I., et al. (2014) · Cell · doi:10.1016/j.cell.2014.07.051 · Cited by 739 · see citing works

Brain-derived neurotrophic factor is produced by skeletal muscle cells in response to contraction and enhances fat oxidation via activation of AMP-activated protein kinase

Matthews, V. B., Åström, M.-B., Chan, M. H. S., Bruce, C. R., Krabbe, K. S., Prelovsek, O., Åkerström, T., Yfanti, C., Broholm, C., Mortensen, O. H., et al. (2009) · Diabetologia · doi:10.1007/s00125-009-1364-1 · Cited by 722 · see citing works

Type 2 diabetes as a risk factor for dementia in women compared with men: a pooled analysis of 2·3 million people comprising more than 100,000 cases of dementia

Chatterjee, S., Peters, S. A. E., Woodward, M., Mejia Arango, S., Batty, G. D., Beckett, N., Beiser, A., Borenstein, A. R., Crane, P. K., Haan, M., et al. (2016) · Diabetes Care · doi:10.2337/dc15-1588 · Cited by 711 · see citing works

Precursor form of brain-derived neurotrophic factor and mature brain-derived neurotrophic factor are decreased in the pre-clinical stages of Alzheimer’s disease

Peng, S., Wuu, J., Mufson, E. J., & Fahnestock, M. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03135.x · Cited by 691 · see citing works

Transport Pathways for Clearance of Human Alzheimer's Amyloid β-Peptide and Apolipoproteins E and J in the Mouse Central Nervous System

Bell, R. D., Sagare, A. P., Friedman, A. E., Bedi, G. S., Holtzman, D. M., Deane, R., & Zlokovic, B. V. (2007) · Journal of Cerebral Blood Flow &amp; Metabolism · doi:10.1038/sj.jcbfm.9600419 · Cited by 670 · see citing works

Alternatively activated microglia and macrophages in the central nervous system

Franco, R., & Fernández‐Suárez, D. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.05.003 · Cited by 650 · see citing works

Running-induced systemic cathepsin B secretion is associated with memory function

Moon, H. Y., Becke, A., Berron, D., Becker, B., Sah, N., Benoni, G., Janke, E., Lubejko, S. T., Greig, N. H., Mattison, J. A., et al. (2016) · Cell Metabolism · doi:10.1016/j.cmet.2016.05.025 · Cited by 628 · see citing works

Lactate Reduces Liver and Pancreatic Injury in Toll-Like Receptor– and Inflammasome-Mediated Inflammation via GPR81-Mediated Suppression of Innate Immunity

Hoque, R., Farooq, A., Ghani, A., Gorelick, F. S., & Mehal, W. Z. (2014) · Gastroenterology · doi:10.1053/j.gastro.2014.03.014 · Cited by 576 · see citing works

Markers of microglia in post-mortem brain samples from patients with Alzheimer’s disease: a systematic review

Hopperton, K. E., Mohammad, D., Trépanier, M. O., Giuliano, V, & Bazinet, R. P. (2018) · Molecular Psychiatry · doi:10.1038/mp.2017.246 · Cited by 567 · see citing works

Exercise induces cerebral VEGF and angiogenesis via the lactate receptor HCAR1

Morland, C., Andersson, K. A., Haugen, Ø. P., Hadzic, A., Kleppa, L., Gille, A., Rinholm, J. E., Palibrk, V., Diget, E. H., Kennedy, L. H., et al. (2017) · Nature Communications · doi:10.1038/ncomms15557 · Cited by 559 · see citing works

The influence of aerobic fitness on cerebral white matter integrity and cognitive function in older adults: Results of a one‐year exercise intervention

Voss, M. W., Heo, S., Prakash, R. S., Erickson, K. I., Alves, H., Chaddock, L., Szabo, A. N., Mailey, E. L., Wójcicki, T. R., White, S. M., et al. (2013) · Human Brain Mapping · doi:10.1002/hbm.22119 · Cited by 553 · see citing works

Lactate mediates the effects of exercise on learning and memory through SIRT1-dependent activation of hippocampal brain-derived neurotrophic factor (BDNF)

El Hayek, L., Khalifeh, M., Zibara, V., Abi Assaad, R., Emmanuel, N., Karnib, N., El-Ghandour, R., Nasrallah, P., Bilen, M., Ibrahim, P., et al. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.1661-18.2019 · Cited by 539 · see citing works

Effect of aerobic exercise on hippocampal volume in humans: A systematic review and meta-analysis

Firth, J., Stubbs, B., Vancampfort, D., Schuch, F., Lagopoulos, J., Rosenbaum, S., & Ward, P. B. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2017.11.007 · Cited by 526 · see citing works

Cerebral Perfusion and the Risk of Dementia

Wolters, F. J., Zonneveld, H. I., Albert Hofman, D., van der Lugt, A., Koudstaal, P. J., Vernooij, M. W., & Ikram, M. A. (2017) · Circulation · doi:10.1161/circulationaha.117.027448 · Cited by 519 · see citing works

Oxidative stress: role of physical exercise and antioxidant nutraceuticals in adulthood and aging

Simioni, C., Zauli, G., Martelli, A. M., Vitale, M., Sacchetti, G., Gonelli, A., & Neri, L. M. (2018) · Oncotarget · doi:10.18632/oncotarget.24729 · Cited by 518 · see citing works

Peripheral Neuron Survival and Outgrowth on Graphene

Convertino, D., Luin, S., Marchetti, L., & Coletti, C. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00001 · Cited by 516 · see citing works

Physical activity predicts gray matter volume in late adulthood: The Cardiovascular Health Study

Erickson, K. I., Raji, C. A., Lopez, O. L., Becker, J. T., Rosano, C., Newman, A. B., Gach, H. M., Thompson, P. M., Ho, A. J., & Kuller, L. H. (2010) · Neurology · doi:10.1212/wnl.0b013e3181f88359 · Cited by 508 · see citing works

Lactate promotes plasticity gene expression by potentiating NMDA signaling in neurons

Yang, J., Ruchti, E., Petit, J.-M., Jourdain, P., Grenningloh, G., Allaman, I., & Magistretti, P. J. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1322912111 · Cited by 504 · see citing works

Subacute Combined Degeneration, Pernicious Anemia and Gastric Neuroendocrine Tumor Occured Simultaneously Caused by Autoimmune Gastritis

Zhang, N., Li, R., Ma, L., Li, N., Shan, P., Wang, X.-B., & Liu, A. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00001 · Cited by 495 · see citing works

Lactate Produced by Glycogenolysis in Astrocytes Regulates Memory Processing

Newman, L. A., Korol, D. L., & Gold, P. E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028427 · Cited by 473 · see citing works

Cognitive activity and incident AD in a population-based sample of older persons

Wilson, R. S., Bennett, D. A., Bienias, J. L., Aggarwal, N. T., Mendes de Leon, C. F., Morris, M. C., Schneider, J. A., & Evans, D. A. (2002) · Neurology · doi:10.1212/01.wnl.0000036905.59156.a1 · Cited by 456 · see citing works

Association Between Elevated Brain Amyloid and Subsequent Cognitive Decline Among Cognitively Normal Persons

Donohue, M. C., Sperling, R. A., Petersen, R., Sun, C.-K., Weiner, M. W., Aisen, P. S., & Initiative, F. T. A. D. N. (2017) · JAMA · doi:10.1001/jama.2017.6669 · Cited by 452 · see citing works

Association Between Sarcopenia and Cognitive Impairment: A Systematic Review and Meta-Analysis

Chang, K. C., Hsu, T.-H., Wu, W., Huang, K., & Han, D. (2016) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2016.09.013 · Cited by 448 · see citing works

Effects of physical activity and exercise on the cognitive function of patients with Alzheimer disease: a meta-analysis

Jia, R., Liang, J., Xu, Y., & Wang, Y. (2019) · BMC Geriatrics · doi:10.1186/s12877-019-1175-2 · Cited by 448 · see citing works

Elevation in cerebral blood flow velocity with aerobic fitness throughout healthy human ageing

Ainslie, P. N., Cotter, J. D., George, K. P., Lucas, S., Murrell, C., Shave, R., Thomas, K. N., Williams, M. J. A., & Atkinson, G. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.158279 · Cited by 444 · see citing works

In vivo staging of regional amyloid deposition

Grothe, M. J., Barthel, H., Sepulcre, J., Dyrba, M., Sabri, O., Teipel, S. J., Initiative, F. T. A. D. N., Initiative, A. D. N., Weiner, M., Aisen, P., et al. (2017) · Neurology · doi:10.1212/wnl.0000000000004643 · Cited by 440 · see citing works

Pathophysiologic relationship between Alzheimer's disease, cerebrovascular disease, and cardiovascular risk: A review and synthesis

Santos, C. Y., Snyder, P. J., Wu, W., Zhang, M., Echeverria, A., & Alber, J. (2017) · Alzheimer's &amp; Dementia: Diagnosis, Assessment &amp; Disease Monitoring · doi:10.1016/j.dadm.2017.01.005 · Cited by 431 · see citing works

A parameter-efficient deep learning approach to predict conversion from mild cognitive impairment to Alzheimer's disease

Spasov, S., Passamonti, L., Duggento, A., Lió, P., & Toschi, N. (2019) · NeuroImage · doi:10.1016/j.neuroimage.2019.01.031 · Cited by 429 · see citing works

Association of Muscle Strength With the Risk of Alzheimer Disease and the Rate of Cognitive Decline in Community-Dwelling Older Persons

Boyle, P. A., Buchman, A. S., Wilson, R. S., Leurgans, S. E., & Bennett, D. A. (2009) · Archives of Neurology · doi:10.1001/archneurol.2009.240 · Cited by 415 · see citing works

Association of plasma clusterin concentration with severity, pathology, and progression in Alzheimer disease

Thambisetty, M., Simmons, A., Velayudhan, L., Hye, A., Campbell, J., Zhang, Y., Wahlund, L.-O., Westman, E., Kinsey, A., Güntert, A., et al. (2010) · Archives of General Psychiatry · doi:10.1001/archgenpsychiatry.2010.78 · Cited by 405 · see citing works

Reduced Lean Mass in Early Alzheimer Disease and Its Association With Brain Atrophy

Burns, J. M., Johnson, D. K., Watts, A. S., Swerdlow, R. H., & Brooks, W. M. (2010) · Archives of Neurology · doi:10.1001/archneurol.2010.38 · Cited by 400 · see citing works

Convolutional Neural Networks-Based MRI Image Analysis for the Alzheimer’s Disease Prediction From Mild Cognitive Impairment

Lin, W.-M., Tong, T., Gao, Q., Guo, D., Du, X., Yang, Y., Guo, G., Xiao, M., Du, M., Qu, X., et al. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00777 · Cited by 391 · see citing works

Clusterin in Alzheimer’s Disease: Mechanisms, Genetics, and Lessons From Other Pathologies

Foster, E. M., Dangla-Valls, A., Lovestone, S., Ribe, E. M., & Buckley, N. J. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00164 · Cited by 381 · see citing works

Weight Loss and Malnutrition in Patients with Parkinson's Disease: Current Knowledge and Future Prospects

Ma, K., Xiong, N., Shen, Y., Han, C., Liu, L., Zhang, G., Wang, L., Guo, S., Guo, X., Xia, Y. F., et al. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00001 · Cited by 379 · see citing works

Changes of some oxidative stress markers in the serum of patients with mild cognitive impairment and Alzheimer's disease

Padurariu, M., Ciobica, A., Hritcu, L., Stoica, B., Bild, W., & Stefanescu, C. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2009.11.033 · Cited by 378 · see citing works

Correction: Corrigendum: Superfast assembly and synthesis of gold nanostructures using nanosecond low-temperature compression via magnetic pulsed power

Li, B., Bian, K., Lane, J. M. D., Salerno, K. M., Grest, G. S., Ao, T., Hickman, R. J., Wise, J. L., Wang, Z., & Fan, H. (2017) · Nature Communications · doi:10.1038/ncomms15574 · Cited by 372 · see citing works

Voluntary Exercise Promotes Glymphatic Clearance of Amyloid Beta and Reduces the Activation of Astrocytes and Microglia in Aged Mice

He, X.-F., Liu, D.-X., Zhang, Q., Liang, F.-Y., Dai, G.-Y., Zeng, J.-S., Pei, Z., Xu, G.-Q., & Lan, Y. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00144 · Cited by 371 · see citing works

Cardiorespiratory fitness and brain atrophy in early Alzheimer disease.

Burns, J. M., Cronk, B. B., Anderson, H. S., Donnelly, J. E., Thomas, G. P., Harsha, A., Brooks, W. M., & Swerdlow, R. H. (2008) · Neurology · doi:10.1212/01.wnl.0000317094.86209.cb · Cited by 363 · see citing works

Functional and/or structural brain changes in response to resistance exercises and resistance training lead to cognitive improvements – a systematic review

Herold, F., Törpel, A., Schega, L., & Müller, N. G. (2019) · European Review of Aging and Physical Activity · doi:10.1186/s11556-019-0217-2 · Cited by 349 · see citing works

Role of nitric oxide in cardiovascular disease: focus on the endothelium

Cannon, R. O. (1998) · Clinical Chemistry · doi:10.1093/clinchem/44.8.1809 · Cited by 346 · see citing works

Exercise and Alzheimer’s disease biomarkers in cognitively normal older adults

Liang, K. Y., Mintun, M. A., Fagan, A. M., Goate, A. M., Bugg, J. M., Holtzman, D. M., Morris, J. C., & Head, D. (2010) · Annals of Neurology · doi:10.1002/ana.22096 · Cited by 340 · see citing works

Oxidative stress in blood in Alzheimer's disease and mild cognitive impairment: A meta-analysis

Schrag, M., Mueller, C., Zabel, M. K., Crofton, A. R., Kirsch, W. M., Ghribi, O., Squitti, R., & Perry, G. L. (2013) · Neurobiology of Disease · doi:10.1016/j.nbd.2013.07.005 · Cited by 335 · see citing works

Associations between vascular risk factors and brain MRI indices in UK Biobank

Cox, S. R., Lyall, D. M., Ritchie, S. J., Bastin, M. E., Harris, M. A., Buchanan, C. R., Fawns‐Ritchie, C., Barbu, M. C., de Nooij, L., Reus, L. M., et al. (2019) · European Heart Journal · doi:10.1093/eurheartj/ehz100 · Cited by 329 · see citing works

The Antioxidant Effect of Exercise: A Systematic Review and Meta-Analysis

Sousa, C. V., Sales, M. M., Rosa, T. D. S., Lewis, J. E., de Andrade, R. V., & Simões, H. G. (2016) · Sports Medicine · doi:10.1007/s40279-016-0566-1 · Cited by 328 · see citing works

The effect of acute exercise on blood concentrations of brain-derived neurotrophic factor in healthy adults. A meta-analysis.

Dinoff, A., Herrmann, N., Swardfager, W., & Lanctôt, K. L. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13603 · Cited by 323 · see citing works

Exercise Plays a Preventive Role Against Alzheimer's Disease

Radak, Z. O., Hart, N., Sarga, L., Koltai, E., Atalay, M., Ohno, H., & Boldogh, I. R. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-091531 · Cited by 316 · see citing works

Chronic voluntary alcohol consumption causes persistent cognitive deficits and cortical cell loss in a rodent model

Charlton, A. J., May, C., Luikinga, S. J., Burrows, E. L., Kim, J. H., Lawrence, A. J., & Perry, C. J. (2019) · Scientific Reports · doi:10.1038/s41598-019-55095-w · Cited by 315 · see citing works

Effects of the Finnish Alzheimer Disease Exercise Trial (FINALEX): A Randomized Controlled Trial

Pitkälä, K. H., Pöysti, M. M., Laakkonen, M.-L., Tilvis, R. S., Savikko, N., Kautiainen, H., & Strandberg, T. E. (2013) · JAMA Internal Medicine · doi:10.1001/jamainternmed.2013.359 · Cited by 304 · see citing works

Kynurenine pathway in depression: a systematic review and meta-analysis

Ogyu, K., Kubo, K., Noda, Y., Iwata, Y., Tsugawa, S., Omura, Y., Wada, M., Tarumi, R., Plitman, E., Moriguchi, S., et al. (2018) · Neuroscience &amp; Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.03.023 · Cited by 301 · see citing works

In vivo staging of regional amyloid deposition

Grothe, M. J., Barthel, H., Sepulcre, J., Dyrba, M., Sabri, O., Teipel, S. J., Stern, Y., & Initiative, A. D. N. (2022) · DZNE Pub · doi:10.7916/0vj1-4c02 · Cited by 294 · see citing works

Decreased plasma antioxidants in patients with Alzheimer's disease

Kim, T., Pae, C., Yoon, S.-J., Jang, W., Lee, N. J., Kim, J.-J., Lee, S., Lee, C., Paik, I.-H., & Lee, C. (2006) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.1469 · Cited by 291 · see citing works

Reward Dependent Invigoration Relates to Theta Oscillations and Is Predicted by Dopaminergic Midbrain Integrity in Healthy Elderly

Steiger, T. K., & Bunzeck, N. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00001 · Cited by 273 · see citing works

Endocrine Crosstalk Between Skeletal Muscle and the Brain

Delezie, J., & Handschin, C. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00698 · Cited by 270 · see citing works

Untitled work

Head (2012) · doi:10.1001/archneurol.2011.845 · Cited by 267 · see citing works

Systems biology: integrating technology, biology, and computation

Hood, L. (2003) · Mechanisms of Ageing and Development · doi:10.1016/s0047-6374(02)00164-1 · Cited by 265 · see citing works

Ten simple rules for reporting voxel-based morphometry studies

Ridgway, G., Henley, S. M. D., Rohrer, J., Scahill, R., Warren, J., & Fox, N. C. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.01.003 · Cited by 263 · see citing works

Functional connectivity: A source of variance in the association between cardiorespiratory fitness and cognition?

Voss, M. W., Erickson, K. I., Prakash, R. S., Chaddock, L., Malkowski, E., Alves, H., Kim, J., Morris, K. S., White, S. M., Wójcicki, T. R., et al. (2010) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2010.01.005 · Cited by 261 · see citing works

Physical Exercise Protects Against Alzheimer's Disease in 3xTg-AD Mice

García‐Mesa, Y., López, J. C., Giménez‐Llort, L., Revilla, S., Guerra, R., Gruart, A., LaFerla, F. M., Cristòfol, R. M., Delgado-Garcia, J. M., & Sanfeliu, C. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-101635 · Cited by 253 · see citing works

Kv2 Ion Channels Determine the Expression and Localization of the Associated AMIGO-1 Cell Adhesion Molecule in Adult Brain Neurons

Bishop, H. I., Cobb, M. M., Kirmiz, M., Parajuli, L. K., Mandikian, D., Philp, A. M., Melnik, M., Kuja‐Panula, J., Rauvala, H., Shigemoto, R., et al. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00001 · Cited by 251 · see citing works

Neuroanatomical correlates of aging, cardiopulmonary fitness level, and education

Gordon, B. A., Rykhlevskaia, E. I., Brumback, C. R., Lee, Y., Elavsky, S., Konopack, J. F., McAuley, E., Kramer, A. F., Colcombe, S. J., Gratton, G., et al. (2008) · Psychophysiology · doi:10.1111/j.1469-8986.2008.00676.x · Cited by 245 · see citing works

Physical activity and memory functions: Are neurotrophins and cerebral gray matter volume the missing link?

Flöel, A., Ruscheweyh, R., Krüger, K., Willemer, C., Winter, B., Völker, K., Lohmann, H., Zitzmann, M., Mooren, F. C., Breitenstein, C., et al. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.10.043 · Cited by 243 · see citing works

High-intensity interval training evokes larger serum BDNF levels compared with intense continuous exercise

Marquez, C. M. S., Vanaudenaerde, B. M., Troosters, T., & Wenderoth, N. (2015) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00126.2015 · Cited by 243 · see citing works

The Association of Tau With Mitochondrial Dysfunction in Alzheimer’s Disease

Cheng, Y., & Bai, F. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00163 · Cited by 239 · see citing works

Exercise moderates age-related atrophy of the medial temporal lobe

Bugg, J. M., & Head, D. M. (2009) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2009.03.008 · Cited by 236 · see citing works

Physical activity and amyloid-β plasma and brain levels: results from the Australian Imaging, Biomarkers and Lifestyle Study of Ageing

Brown, B. M., Peiffer, J. J., Taddei, K., Lui, J. K., Laws, S. M., Gupta, V. B., Taddei, T., Ward, V. K., Rodrigues, M. A., Burnham, S., et al. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.107 · Cited by 235 · see citing works

Obesity as a risk factor for Alzheimer's disease: weighing the evidence

Alford, S., Patel, D. K., Perakakis, N., & Mantzoros, C. S. (2017) · Obesity Reviews · doi:10.1111/obr.12629 · Cited by 219 · see citing works

Treadmill Exercise Exerts Neuroprotection and Regulates Microglial Polarization and Oxidative Stress in a Streptozotocin-Induced Rat Model of Sporadic Alzheimer’s Disease

Lu, Y., Dong, Y., Tucker, D., Wang, R., Ahmed, M. E., Brann, D. W., & Zhang, Q. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-160869 · Cited by 214 · see citing works

Midlife Blood Pressure, Plasma β-Amyloid, and the Risk for Alzheimer Disease

Shah, N. S., Vidal, J., Masaki, K., Petrovitch, H., Ross, G. W., Tilley, C., Demattos, R. B., Tracy, R. P., White, L. R., & Launer, L. J. (2012) · Hypertension · doi:10.1161/hypertensionaha.111.178962 · Cited by 212 · see citing works

Diabetes Mellitus and Dementia

Ninomiya, T. (2014) · Current Diabetes Reports · doi:10.1007/s11892-014-0487-z · Cited by 211 · see citing works

Cardiorespiratory Fitness and Preserved Medial Temporal Lobe Volume in Alzheimer Disease

Honea, R. A., Thomas, G., Harsha, A., Anderson, H. S., Donnelly, J. E., Brooks, W. M., & Burns, J. M. (2009) · Alzheimer Disease & Associated Disorders · doi:10.1097/wad.0b013e31819cb8a2 · Cited by 211 · see citing works

Association of brain amyloid-β with cerebral perfusion and structure in Alzheimer’s disease and mild cognitive impairment

Mattsson, N., Tosun, D., Insel, P. S., Simonson, A., Jack, C. R., Beckett, L. A., Donohue, M., Jagust, W., Schuff, N. W., & Weiner, M. W. (2014) · Brain · doi:10.1093/brain/awu043 · Cited by 211 · see citing works

Regulation of Mitochondrial Biogenesis in Muscle by Endurance Exercise

Irrcher, I., Adhihetty, P. J., Joseph, A.-M., Ljubicic, V., & Hood, D. A. (2003) · Sports Medicine · doi:10.2165/00007256-200333110-00001 · Cited by 210 · see citing works

Resistance exercise induces a greater irisin response than endurance exercise

Tsuchiya, Y., Ando, D., Takamatsu, K., & Goto, K. (2015) · Metabolism · doi:10.1016/j.metabol.2015.05.010 · Cited by 207 · see citing works

Physical activity can improve cognition in patients with Alzheimer’s disease: a systematic review and meta-analysis of randomized controlled trials

Du, Z., Li, Y., Li, J., Zhou, C., Li, F., & Yang, X. (2018) · Clinical Interventions in Aging · doi:10.2147/cia.s169565 · Cited by 203 · see citing works

Acute Aerobic Exercise Increases Brain-Derived Neurotrophic Factor Levels in Elderly with Alzheimer's Disease

Coelho, F. G. D. M., Vital, T. M., Stein, A. M., Arantes, F. J., Rueda, A. V., Camarini, R., Teodorov, E., & Santos-Galduróz, R. F. (2014) · Journal of Alzheimer's Disease · doi:10.3233/jad-131073 · Cited by 203 · see citing works

Characterization of Apolipoprotein J-Alzheimer's Aβ Interaction

Matsubara, E., Frangione, B., & Ghiso, J. A. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.13.7563 · Cited by 195 · see citing works

Exercise-induced brain-derived neurotrophic factor expression: Therapeutic implications for Alzheimer’s dementia

Wang, R., & Holsinger, R. M. D. (2018) · Ageing Research Reviews · doi:10.1016/j.arr.2018.10.002 · Cited by 194 · see citing works

Physical activity and dementia risk in the elderly

Ravaglia, G., Forti, P., Lucicesare, A., Pisacane, N., Rietti, E., Bianchin, M., & Dalmonte, E. (2007) · Neurology · doi:10.1212/01.wnl.0000296276.50595.86 · Cited by 191 · see citing works

Association of body mass index and waist-to-hip ratio with brain structure

Hamer, M., & Batty, G. D. (2019) · Neurology · doi:10.1212/wnl.0000000000006879 · Cited by 190 · see citing works

Effects of Physical Exercise on Neuroinflammation, Neuroplasticity, Neurodegeneration, and Behavior

Svensson, M., Lexell, J. E., & Deierborg, T. (2014) · Neurorehabilitation and neural repair · doi:10.1177/1545968314562108 · Cited by 189 · see citing works

Revolution of Alzheimer Precision Neurology. Passageway of Systems Biology and Neurophysiology

Hampel, H. J., (APMI), F. T. A. P. M. I., Toschi, N., Babiloni, C., Baldacci, F., Black, K. L., Bokde, A. L. W., Bun, R. S., Cacciola, F., Cavedo, E., et al. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-179932 · Cited by 181 · see citing works

The Role of Clusterin in Alzheimer’s Disease: Pathways, Pathogenesis, and Therapy

Yu, J.-T., & Tan, L. (2012) · Molecular Neurobiology · doi:10.1007/s12035-012-8237-1 · Cited by 174 · see citing works

Can Exercise Improve Cognitive Symptoms of Alzheimer's Disease?

Panza, G. A., Taylor, B. A., MacDonald, H. V., Johnson, B. T., Zaleski, A. L., Livingston, J. M., Thompson, P. D., & Pescatello, L. S. (2018) · Journal of the American Geriatrics Society · doi:10.1111/jgs.15241 · Cited by 174 · see citing works

Hippocampal plasticity underpins long-term cognitive gains from resistance exercise in MCI

Broadhouse, K. M., Singh, M. F., Suo, C., Gates, N., Wen, W., Brodaty, H., Jain, N., Wilson, G. C., Meiklejohn, J., Singh, N., et al. (2020) · NeuroImage: Clinical · doi:10.1016/j.nicl.2020.102182 · Cited by 172 · see citing works

Sarcopenia and Muscle Functions at Various Stages of Alzheimer Disease

Ogawa, Y., Kaneko, Y., Sato, T., et al. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00710 · Cited by 169 · see citing works

Cerebral Perfusion Imaging in Alzheimer's Disease

Johnson, K. A. (1987) · Archives of Neurology · doi:10.1001/archneur.1987.00520140035014 · Cited by 168 · see citing works

Alzheimer’s Disease Mutant Mice Exhibit Reduced Brain Tissue Stiffness Compared to Wild-type Mice in both Normoxia and following Intermittent Hypoxia Mimicking Sleep Apnea

Menal, M. J., Jorba, I., Torres, M., Montserrat, J. M., Gozal, D., Colell, A., Piñol‐Ripoll, G., Navajas, D., Almendros, I., & Farré, R. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.00001 · Cited by 166 · see citing works

Novel ketone diet enhances physical and cognitive performance

Murray, A. J., Knight, N. S., Cole, M. A., Cochlin, L. E., Carter, E., Tchabanenko, K., Pichulik, T., Gulston, M. K., Atherton, H. J., Schroeder, M., et al. (2016) · The FASEB Journal · doi:10.1096/fj.201600773r · Cited by 165 · see citing works

Physical Activity and Alzheimer Disease: A Protective Association

Santos-Lozano, A., Pareja-Galeano, H., Sanchis-Gomar, F., Quindós-Rubial, M., Fiuza-Luces, C., Cristi-Montero, C., Emanuele, E., Garatachea, N., & Lucia, A. (2016) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2016.04.024 · Cited by 164 · see citing works

Exercise Training and Functional Connectivity Changes in Mild Cognitive Impairment and Healthy Elders

Chirles, T. J., Reiter, K. E., Weiss, L. R., Alfini, A. J., Nielson, K. A., & Smith, J. C. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-161151 · Cited by 164 · see citing works

Lactate Inhibits the Pro-Inflammatory Response and Metabolic Reprogramming in Murine Macrophages in a GPR81-Independent Manner

Errea, A. J., Cayet, D., Marchetti, P., Tang, C., Kluza, J., Offermanns, S., Sirard, J., & Rumbo, M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0163694 · Cited by 161 · see citing works

Lactate infusion at rest increases BDNF blood concentration in humans.

Schiffer, T., Schulte, S., Sperlich, B., Achtzehn, S., Fricke, H., & Strüder, H. K. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2010.11.035 · Cited by 159 · see citing works

Associations of Physical Activity and β-Amyloid With Longitudinal Cognition and Neurodegeneration in Clinically Normal Older Adults

Rabin, J. S., Klein, H., Kirn, D. R., Schultz, A. P., Yang, H., Hampton, O. L., Jiang, S., Buckley, R. F., Viswanathan, A., Hedden, T., et al. (2019) · JAMA Neurology · doi:10.1001/jamaneurol.2019.1879 · Cited by 155 · see citing works

Diet modulates brain network stability, a biomarker for brain aging, in young adults

Mujica-Parodi, L. R., Amgalan, A., Sultan, S. F., Antal, B. B., Sun, X., Skiena, S., Lithen, A., Adra, N., Ratai, E., Weistuch, C., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1913042117 · Cited by 155 · see citing works

Lower cerebral blood flow is associated with impairment in multiple cognitive domains in Alzheimer's disease

Leeuwis, A. E., Benedictus, M. R., Kuijer, J. P. A., Binnewijzend, M. A. A., Hooghiemstra, A. M., Verfaillie, S. C. J., Koene, T., Scheltens, P., Barkhof, F., Prins, N. D., et al. (2016) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2016.08.013 · Cited by 150 · see citing works

Life‐long aerobic exercise preserved baseline cerebral blood flow but reduced vascular reactivity to CO 2

Thomas, B. P., Yezhuvath, U. S., Tseng, B. Y., Liu, P., Levine, B. D., Zhang, R., & Lu, H. (2013) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.24090 · Cited by 150 · see citing works

Interactive effects of fitness and hormone treatment on brain health in postmenopausal women

Erickson, K. I., Colcombe, S. J., Elavsky, S., McAuley, E., Korol, D. L., Scalf, P. E., & Kramer, A. F. (2006) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.11.016 · Cited by 148 · see citing works

A Precision Medicine Initiative for Alzheimer’s disease: the road ahead to biomarker-guided integrative disease modeling

Hampel, H., O’Bryant, S. E., Durrleman, S., Younesi, E., Rojkova, K., Escott-Price, V., Corvol, J.-C., Broich, K., Dubois, B., Lista, S., et al. (2017) · Climacteric · doi:10.1080/13697137.2017.1287866 · Cited by 147 · see citing works

Exercise reduces activation of microglia isolated from hippocampus and brain of aged mice

Kohman, R. A., Bhattacharya, T. K., Wojcik, E., & Rhodes, J. S. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-114 · Cited by 146 · see citing works

Role of Aerobic Fitness and Aging on Cerebral White Matter Integrity

Marks, B. L., Madden, D. J., Bucur, B., Provenzale, J. M., WHITE, L. E., Cabeza, R. E. L., & Huettel, S. A. (2007) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1379.022 · Cited by 145 · see citing works

High intensity training in obesity: a Meta-analysis

Türk, Y., Theel, W., Kasteleyn, M. J., Franssen, F. M. E., Hiemstra, P. S., Rudolphus, A., Taube, C., & Braunstahl, G. J. (2017) · Obesity Science &amp; Practice · doi:10.1002/osp4.109 · Cited by 142 · see citing works

Effect of aerobic training and resistance training on circulating irisin level and their association with change of body composition in overweight/obese adults: a pilot study

KIM, H.-J., LEE, H.-J., SO, B., SON, J. S., YOON, D., & SONG, W. (2016) · Physiological Research · doi:10.33549/physiolres.932997 · Cited by 141 · see citing works

The association between physical activity and dementia in an elderly population: the Rotterdam Study

de Bruijn, R. F. A. G., Schrijvers, E. M. C., de Groot, K. A., Witteman, J. C. M., Albert Hofman, D., Franco, O. H., Koudstaal, P. J., & Ikram, M. A. (2013) · European Journal of Epidemiology · doi:10.1007/s10654-013-9773-3 · Cited by 140 · see citing works

Decreased peripheral brain-derived neurotrophic factor levels in Alzheimer’s disease: a meta-analysis study (N=7277)

Qin, X.-Y., Cao, C., Cawley, N. X., Liu, T.-T., Yuan, J., Loh, Y. P., & Cheng, Y. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.62 · Cited by 134 · see citing works

Cerebral changes improved by physical activity during cognitive decline: A systematic review on MRI studies

Haeger, A., Costa, A. S., Schulz, J. B., & Reetz, K. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101933 · Cited by 133 · see citing works

Alzheimer's Disease: The Role of Microglia in Brain Homeostasis and Proteopathy

Clayton, K. A., Enoo, A. A. V., & Ikezu, T. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00680 · Cited by 132 · see citing works

Comparing interval and continuous exercise training regimens on neurotrophic factors in rat brain

Afzalpour, M. E., Chadorneshin, H. T., Foadoddini, M., & Eivari, H. A. (2015) · Physiology &amp; Behavior · doi:10.1016/j.physbeh.2015.04.012 · Cited by 131 · see citing works

Low-Intensity Exercise Exerts Beneficial Effects on Plasma Lipids via PPARγ

BUTCHER, L. R., THOMAS, A., BACKX, K., ROBERTS, A., WEBB, R., & MORRIS, K. (2008) · Medicine &amp; Science in Sports &amp; Exercise · doi:10.1249/mss.0b013e31816c091d · Cited by 128 · see citing works

Oxidative Stress Is a Central Target for Physical Exercise Neuroprotection Against Pathological Brain Aging

García‐Mesa, Y., Colié, S., Corpas, R., Cristòfol, R. M., Comellas, F., Nebreda, Á. R., Giménez‐Llort, L., & Sanfeliu, C. (2015) · The Journals of Gerontology Series A · doi:10.1093/gerona/glv005 · Cited by 124 · see citing works

Effect of Exercise on Inflammatory Profile of Older Persons: Systematic Review and Meta-Analyses

Monteiro-Júnior, R. S., Maciel-Pinheiro, P. D. T., Portugal, E. M. M., Figueiredo, L. F. D. S., Terra, R., Carneiro, L. S. R. D. S. F., Rodrigues, V. D., Nascimento, O. J. M., Deslandes, A. C., & Laks, J. (2017) · Journal of Physical Activity and Health · doi:10.1123/jpah.2016-0735 · Cited by 123 · see citing works

The effect of high Intensity interval training versus moderate intensity continuous training on arterial stiffness and 24 h blood pressure responses: A systematic review and meta-analysis

Way, K. L., Sultana, R. N., Sabag, A., Baker, M. K., & Johnson, N. A. (2018) · Journal of science and medicine in sport · doi:10.1016/j.jsams.2018.09.228 · Cited by 122 · see citing works

No difference in the skeletal muscle angiogenic response to aerobic exercise training between young and aged men

Gavin, T. P., Ruster, R. S., Carrithers, J. A., Zwetsloot, K. A., Kraus, R. M., Evans, C. A., Knapp, D. J., Drew, J. L., McCartney, J. S., Garry, J. P., et al. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.143198 · Cited by 121 · see citing works

Lower cerebral blood flow is associated with faster cognitive decline in Alzheimer’s disease

Benedictus, M. R., Leeuwis, A. E., Binnewijzend, M. A. A., Kuijer, J. P. A., Scheltens, P., Barkhof, F., van der Flier, W. M., & Prins, N. D. (2016) · European Radiology · doi:10.1007/s00330-016-4450-z · Cited by 118 · see citing works

L-Lactate Regulates the Expression of Synaptic Plasticity and Neuroprotection Genes in Cortical Neurons: A Transcriptome Analysis

Margineanu, M. B., Mahmood, H., Fiumelli, H., & Magistretti, P. J. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00375 · Cited by 117 · see citing works

A multi-center comparison of o2peak trainability between interval training and moderate intensity continuous training.

Williams, C. J., Gurd, B. J., Bonafiglia, J. T., Voisin, S., Li, Z., Harvey, N., Croci, I., Taylor, J. L., Gajanand, T., Ramos, J. S., et al. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00019 · Cited by 117 · see citing works

Exercise intensity affects acute neurotrophic and neurophysiological responses poststroke

Boyne, P., Meyrose, C., Westover, J., Whitesel, D., Hatter, K., Reisman, D. S., Cunningham, D. A., Carl, D., Jansen, C., Khoury, J. C., et al. (2018) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00594.2018 · Cited by 117 · see citing works

PRECISION MEDICINE - THE GOLDEN GATE FOR DETECTION, TREATMENT AND PREVENTION OF ALZHEIMER’S DISEASE

Hampel, H. J., O’Bryant, S. E., Castrillo, J. I., Ritchie, C. W., Rojkova, K., Broich, K., Benda, N., Nisticò, R., Frank, R., Dubois, B., et al. (2016) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2016.112 · Cited by 116 · see citing works

A brief primer on the mediational role of <scp>BDNF</scp> in the exercise‐memory link

Loprinzi, P. D., & Frith, E. (2019) · Clinical Physiology and Functional Imaging · doi:10.1111/cpf.12522 · Cited by 116 · see citing works

Effect of aerobic exercise on physical performance in patients with Alzheimer's disease

Sobol, N. A., Hoffmann, K., Frederiksen, K. S., Vogel, A., Vestergaard, K., Brændgaard, H., Gottrup, H., Lolk, A., Wermuth, L., Jakobsen, S., et al. (2016) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2016.05.004 · Cited by 114 · see citing works

Brain Perfusion Change in Patients with Mild Cognitive Impairment After 12 Months of Aerobic Exercise Training

Thomas, B. P., Tarumi, T., Sheng, M., Tseng, B. Y., Womack, K. B., Cullum, C. M., Bart Rypma, A., Zhang, R., & Lu, H. (2020) · Journal of Alzheimer s Disease · doi:10.3233/jad-190977 · Cited by 113 · see citing works

Brain Network Modularity Predicts Exercise-Related Executive Function Gains in Older Adults

Baniqued, P. L., Gallen, C. L., Voss, M. W., Burzynska, A. Z., Wong, C. N., Cooke, G. E., Duffy, K., Fanning, J., Ehlers, D. K., Salerno, E. A., et al. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00426 · Cited by 112 · see citing works

Increased Protein and Lipid Oxidative Damage in Mitochondria Isolated from Lymphocytes from Patients with Alzheimer's Disease: Insights into the Role of Oxidative Stress in Alzheimer's Disease and Initial Investigations into a Potential Biomarker for this Dementing Disorder

Sultana, R., Mecocci, P., Mangialasche, F., Cecchetti, R., Baglioni, M., & Butterfield, D. A. (2011) · Journal of Alzheimer's Disease · doi:10.3233/jad-2011-101425 · Cited by 111 · see citing works

A Ketogenic Diet Improves Cognition and Has Biochemical Effects in Prefrontal Cortex That Are Dissociable From Hippocampus

Hernandez, A. R., Hernandez, C. M., Campos, K., Truckenbrod, L., Federico, Q., Moon, B., McQuail, J. A., Maurer, A. P., Bizon, J. L., & Burke, S. N. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00391 · Cited by 111 · see citing works

Physical Exercise and Brain Mitochondrial Fitness: The Possible Role Against <scp>A</scp>lzheimer's Disease

Bernardo, T. C., Marques‐Aleixo, I., Beleza, J., Oliveira, P. J., Ascensão, A., & Magalhães, J. (2016) · Brain Pathology · doi:10.1111/bpa.12403 · Cited by 108 · see citing works

The Alzheimer Precision Medicine Initiative

Hampel, H. J., Initiative, A. P. M., Vergallo, A., Perry, G. L., & Lista, S. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-181121 · Cited by 108 · see citing works

Exercise amelioration of depression-like behavior in OVX mice is associated with suppression of NLRP3 inflammasome activation in hippocampus

Wang, Y., Xu, Y., Sheng, H., Ni, X., & Lu, J. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.03.044 · Cited by 106 · see citing works

Omics and Exercise: Global Approaches for Mapping Exercise Biological Networks.Preprint

Hoffman, N. J. (2017) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a029884 · Cited by 106 · see citing works

Does exercise reduce brain oxidative stress? A systematic review

Camiletti‐Moirón, D., Aparicio, V. A., Aranda, P., & Radak, Z. (2013) · Scandinavian Journal of Medicine &amp; Science in Sports · doi:10.1111/sms.12065 · Cited by 104 · see citing works

Impact of resistance training on the autophagy-inflammation-apoptosis crosstalk in elderly subjects

Mejías-Peña, Y., Estébanez, B., Rodriguez-Miguelez, P., Fernandez-Gonzalo, R., Almar, M., de Paz, J. A., González-Gallego, J., & Cuevas, M. J. (2017) · Aging · doi:10.18632/aging.101167 · Cited by 102 · see citing works

Oxidative Stress, Antioxidants, and Alzheimer Disease

Rottkamp, C. A., Nunomura, A., Raina, A. K., Sayre, L. M., Perry, G. L., & Smith, M. A. (2000) · Alzheimer Disease & Associated Disorders · doi:10.1097/00002093-200000001-00010 · Cited by 100 · see citing works

The antibacterial effect of non-thermal atmospheric pressure plasma treatment of titanium surfaces according to the bacterial wall structure

Lee, M.-J., Kwon, J., Jiang, H. B., Choi, E. H., Park, G., & Kim, K. (2019) · Scientific Reports · doi:10.1038/s41598-019-39414-9 · Cited by 100 · see citing works

Distribution and Numbers of Pygmies in Central African Forests

Olivero, J., Fa, J. E., Farfán, M. Á., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0144499 · Cited by 98 · see citing works

Physical Exercise Improves Cognitive Function Together with Microglia Phenotype Modulation and Remyelination in Chronic Cerebral Hypoperfusion

Jiang, T., Zhang, L., Pan, X., Zheng, H., Chen, X., Li, L., Luo, J., & Hu, X. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00404 · Cited by 90 · see citing works

Lactate potentiates angiogenesis and neurogenesis in experimental intracerebral hemorrhage

Zhou, J., Liu, T., Guo, H., Cui, H., Li, P., Feng, D., Hu, E., Huang, Q. B., Yang, A., Zhou, J., et al. (2018) · Experimental & Molecular Medicine · doi:10.1038/s12276-018-0113-2 · Cited by 90 · see citing works

Beta-hydroxybutyrate Promotes the Expression of BDNF in Hippocampal Neurons under Adequate Glucose Supply

Hu, E., Du, H., Zhu, X., Wang, L., Shang, S., Wu, X., Lü, H., & Lu, X. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.06.036 · Cited by 88 · see citing works

Exercise Training in Amnestic Mild Cognitive Impairment: A One-Year Randomized Controlled Trial

Tarumi, T., Rossetti, H. C., Thomas, B. P., Harris, T. S., Tseng, B. Y., Turner, M., Wang, C., German, Z., Martin‐Cook, K., Stowe, A. M., et al. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-181175 · Cited by 87 · see citing works

Effects of physical exercise on Alzheimer's disease biomarkers: a systematic review of intervention studies

Frederiksen, K. S., Gjerum, L., Waldemar, G., & Hasselbalch, S. G. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-170567 · Cited by 86 · see citing works

Exercise-Related Changes of Networks in Aging and Mild Cognitive Impairment Brain

Huang, P., Fang, R., Li, B., & Chen, S. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00047 · Cited by 85 · see citing works

High-coverage genomes to elucidate the evolution of penguins

Pan, H., Cole, T. L., Bi, X., Fang, M., Zhou, C., Yang, Z., Ksepka, D. T., Hart, T., Bouzat, J. L., Argilla, L. S., et al. (2019) · GigaScience · doi:10.1093/gigascience/giz117 · Cited by 84 · see citing works

Exercise-associated generation of PPARγ ligands activates PPARγ signaling events and upregulates genes related to lipid metabolism

Thomas, A. W., Davies, N. A., Moir, H. J., Watkeys, L. J., Ruffino, J. S., Isa, S., Butcher, L., Hughes, M. G., Morris, K., & Webb, R. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00864.2011 · Cited by 81 · see citing works

Short‐time high‐intensity exercise increases peripheral BDNF in a physical fitness‐dependent way in healthy men

Antunes, B. M., Rossi, F. E., Teixeira, A. M. A. J., & Lira, F. S. (2019) · European Journal of Sport Science · doi:10.1080/17461391.2019.1611929 · Cited by 74 · see citing works

Oxidative stress and pro-inflammatory cytokines may act as one of the signals for regulating microRNAs expression in Alzheimer’s disease

Prasad, K. N. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.12.003 · Cited by 71 · see citing works

Exercise as ‘precision medicine’ for insulin resistance and its progression to type 2 diabetes: a research review

DiMenna, F. J., & Arad, A. D. (2018) · BMC Sports Science, Medicine and Rehabilitation · doi:10.1186/s13102-018-0110-8 · Cited by 68 · see citing works

Adverse Vascular Risk is Related to Cognitive Decline in Older Adults

Jefferson, A. L., Hohman, T. J., Liu, D., Haj-Hassan, S., Gifford, K. A., Benson, E. M., Skinner, J. S., Lu, Z., Sparling, J. L., Sumner, E. C., et al. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-141812 · Cited by 67 · see citing works

The peroxisome proliferator‐activated receptors in cardiovascular diseases: experimental benefits and clinical challenges

Cheang, W. S., Tian, X. Y., Wong, W. T., & Huang, Y. (2014) · British Journal of Pharmacology · doi:10.1111/bph.13029 · Cited by 66 · see citing works

Inflammasome Involvement in Alzheimer’s Disease

Olsen, I., & Singhrao, S. K. (2016) · Journal of Alzheimer s Disease · doi:10.3233/jad-160197 · Cited by 66 · see citing works

The Effects of Acute and Chronic Aerobic Activity on the Signaling Pathway of the Inflammasome NLRP3 Complex in Young Men

Abkenar, I. K., Rahmani‐Nia, F., & Lombardi, G. (2019) · Medicina · doi:10.3390/medicina55040105 · Cited by 64 · see citing works

Prevention and Treatment of Alzheimer’s Disease: Biological Mechanisms of Exercise

McGurran, H., Glenn, J. M., Madero, E. N., & Bott, N. T. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-180958 · Cited by 63 · see citing works

Modulation of Amyloid-β1–40 Transport by ApoA1 and ApoJ Across an in vitro Model of the Blood-Brain Barrier

Merino-Zamorano, C., Fernández-de Retana, S., Montañola, A., Batlle, A., Saint-Pol, J., Mysiorek, C., Gosselet, F., Montaner, J., & Hernández-Guillamon, M. (2016) · Journal of Alzheimer's Disease · doi:10.3233/jad-150976 · Cited by 63 · see citing works

Habitual exercise levels are associated with cerebral amyloid load in presymptomatic autosomal dominant Alzheimer's disease

Brown, B. M., Sohrabi, H. R., Taddei, K., Gardener, S. L., Rainey‐Smith, S. R., Peiffer, J. J., Xiong, C., Fagan, A. M., Benzinger, T. L. S., Buckles, V., et al. (2017) · Alzheimer s & Dementia · doi:10.1016/j.jalz.2017.03.008 · Cited by 63 · see citing works

Neurexin 3 transmembrane and soluble isoform expression and splicing haplotype are associated with neuron inflammasome and Alzheimer’s disease

Hishimoto, A., Pletnikova, O., Lang, D. L., Troncoso, J. C., Egan, J. M., & Liu, Q.-R. (2019) · Alzheimer's Research &amp; Therapy · doi:10.1186/s13195-019-0475-2 · Cited by 62 · see citing works

Physical activity as a model for health neuroscience

Stillman, C. M., & Erickson, K. I. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13669 · Cited by 53 · see citing works

Peripheral administration of human recombinant ApoJ/clusterin modulates brain beta-amyloid levels in APP23 mice

de Retana, S. F., Marazuela, P., Solé, M., Colell, G., Bonaterra‐Pastra, A., Sánchez‐Quesada, J. L., Montaner, J., Maspoch, D., Cano‐Sarabia, M., & Hernández‐Guillamón, M. (2019) · Alzheimer s Research & Therapy · doi:10.1186/s13195-019-0498-8 · Cited by 53 · see citing works

Clusterin Associates Specifically with <scp>A</scp>β40 in <scp>A</scp>lzheimer's Disease Brain Tissue

Howlett, D. R., Hortobágyi, T., & Francis, P. T. (2013) · Brain Pathology · doi:10.1111/bpa.12057 · Cited by 51 · see citing works

Multiple Diffusion Indices Reveals White Matter Degeneration in Alzheimer's Disease and Mild Cognitive Impairment: A Tract-Based Spatial Statistics Study

Shu, N., Wang, Z., Qi, Z., Li, K., & Yong He, A. (2011) · Journal of Alzheimer s Disease · doi:10.3233/jad-2011-0024 · Cited by 51 · see citing works

MULTIMODAL AFFECT MODELING AND RECOGNITION FOR EMPATHIC ROBOT COMPANIONS

CASTELLANO, G., LEITE, I., PEREIRA, A., MARTINHO, C., PAIVA, A., & MCOWAN, P. W. (2013) · International Journal of Humanoid Robotics · doi:10.1142/s0219843613500102 · Cited by 51 · see citing works

Framingham risk score can predict cognitive decline progression in Alzheimer's disease

Viticchi, G., Falsetti, L., Buratti, L., Boria, C., Luzzi, S., Bartolini, M., Provinciali, L., & Silvestrini, M. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.07.023 · Cited by 49 · see citing works

Alzheimer’s as a Systems-Level Disease Involving the Interplay of Multiple Cellular Networks

Castrillo, J. I., & Oliver, S. G. (2016) · Methods in Molecular Biology · doi:10.1007/978-1-4939-2627-5_1 · Cited by 44 · see citing works

Systems Biology Methods for Alzheimer’s Disease Research Toward Molecular Signatures, Subtypes, and Stages and Precision Medicine: Application in Cohort Studies and Trials

Castrillo, J. I., Lista, S., Hampel, H. J., & Ritchie, C. W. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7704-8_3 · Cited by 44 · see citing works

Physical Activity as a Moderator of Alzheimer Pathology: A Systematic Review of Observational Studies

Frederiksen, K. S., Gjerum, L., Waldemar, G., & Hasselbalch, S. G. (2019) · Current Alzheimer Research · doi:10.2174/1567205016666190315095151 · Cited by 40 · see citing works

Cerebral White Matter Integrity in Amnestic Mild Cognitive Impairment: A 1-Year Randomized Controlled Trial of Aerobic Exercise Training

Tarumi, T., Thomas, B. P., Tseng, B. Y., Wang, C., Womack, K. B., Hynan, L. S., Lu, H., Cullum, C. M., & Zhang, R. (2019) · Journal of Alzheimer s Disease · doi:10.3233/jad-190875 · Cited by 40 · see citing works

Moderate‐ to high‐intensity exercise does not modify cortical β‐amyloid in Alzheimer's disease

Frederiksen, K. S., Madsen, K., Andersen, B. B., Beyer, N., Garde, E., Høgh, P., Waldemar, G., Hasselbalch, S. G., & Law, I. G. (2019) · Alzheimer s & Dementia Translational Research & Clinical Interventions · doi:10.1016/j.trci.2019.04.006 · Cited by 37 · see citing works

Cardiorespiratory Fitness and White Matter Neuronal Fiber Integrity in Mild Cognitive Impairment

Ding, K., Tarumi, T., Zhu, D. C., Tseng, B. Y., Thomas, B. P., Turner, M., Repshas, J., Kerwin, D. R., Womack, K. B., Lu, H., et al. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-170415 · Cited by 37 · see citing works

Exercise, Fitness and the Aging Brain: A Review of Functional Connectivity in Aging

Stillman, C. M., Donofry, S. D., & Erickson, K. I. (2019) · Archives of Psychology · doi:10.31296/aop.v3i4.98 · Cited by 37 · see citing works

Exerkines in health, resilience and disease

Chow, L. S., Gerszten, R. E., Taylor, J. M., Pedersen, B. K., van Praag, H., Trappe, S., Febbraio, M. A., Galis, Z. S., Gao, Y., Haus, J. M., et al. (2022) · Nature Reviews Endocrinology · doi:10.1038/s41574-022-00641-2 · Cited by 927 · see citing works

Brain-Derived Neurotrophic Factor in Alzheimer’s Disease and Its Pharmaceutical Potential

Gao, L., Zhang, Y., Sterling, K., & Song, W. (2022) · Translational Neurodegeneration · doi:10.1186/s40035-022-00279-0 · Cited by 606 · see citing works

Nutrition, physical activity, and other lifestyle factors in the prevention of cognitive decline and dementia

Dominguez, L. J., Veronese, N., Vernuccio, L., Catanese, G., Inzerillo, F., Salemi, G., & Barbagallo, M. (2021) · Nutrients · doi:10.3390/nu13114080 · Cited by 433 · see citing works

Exercise sustains the hallmarks of health

Qiu, Y., Fernández-García, B., Lehmann, H. I., Li, G., Kroemer, G., López-Otín, C., & Xiao, J. (2023) · Journal of Sport and Health Science · doi:10.1016/j.jshs.2022.10.003 · Cited by 270 · see citing works

Antiageing strategy for neurodegenerative diseases: from mechanisms to clinical advances

Jiang, Q., Liu, J., Huang, S., Wang, X.-Y., Chen, X., Liu, G.-H., Ye, K., Song, W., Masters, C. L., Wang, J., et al. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02145-7 · Cited by 165 · see citing works

Exercise interventions in Alzheimer’s disease: A systematic review and meta-analysis of randomized controlled trials

López-Ortiz, S., Valenzuela, P. L., Seisdedos, M. M., Morales, J. S., Vega, T., Castillo-García, A., Nisticò, R., Mercuri, N. B., Lista, S., Lucia, A., et al. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101479 · Cited by 152 · see citing works

New therapeutics beyond amyloid-β and tau for the treatment of Alzheimer’s disease

Zhang, F., Zhong, R.-J., Cheng, C., Li, S., & Le, W.-D. (2021) · Acta Pharmacologica Sinica · doi:10.1038/s41401-020-00565-5 · Cited by 105 · see citing works

Physical Exercise-Induced Myokines in Neurodegenerative Diseases

Lee, B., Shin, M., Park, Y., Won, S.-Y., & Cho, K. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115795 · Cited by 79 · see citing works

Effect of Physical Exercise on Cognitive Function of Alzheimer’s Disease Patients: A Systematic Review and Meta-Analysis of Randomized Controlled Trial

Liu, W., Zhang, J., Wang, Y., Li, J., Chang, J., & Jia, Q. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.927128 · Cited by 50 · see citing works

Resilience by design: How nature, nurture, environment, and microbiome mitigate stress and allostatic load

Chbeir, S., & Carrión, V. (2023) · World Journal of Psychiatry · doi:10.5498/wjp.v13.i5.144 · Cited by 25 · see citing works

Proteomic analysis of secreted proteins from skeletal muscle cells during differentiation

Ojima, K., Oe, M., Nakajima, I., Shibata, M., CHIKUNI, K., Muroya, S., & Nishimura, T. (2014) · EuPA Open Proteomics · doi:10.1016/j.euprot.2014.08.001 · Cited by 29 · see citing works

Muscle-to-organ cross talk mediated by myokines

Pedersen, L., & Højman, P. (2012) · Adipocyte · doi:10.4161/adip.20344 · Cited by 134 · see citing works

Myokines in insulin resistance and type 2 diabetes

Eckardt, K., Görgens, S. W., Raschke, S., & Eckel, J. (2014) · Diabetologia · doi:10.1007/s00125-014-3224-x · Cited by 221 · see citing works

The Effect of Physical Activity on the Secretory Function of Muscles and Bone Tissue in Humans

Траверсе, Г., Горошко, В. І., & Danylchenko, S. I. (2023) · Ukraïnsʹkij žurnal medicini bìologìï ta sportu · doi:10.26693/jmbs08.01.050 · Cited by 2 · see citing works

Skeletal muscle as a gene regulatory endocrine organ

Karstoft, K., & Pedersen, B. K. (2016) · Current Opinion in Clinical Nutrition &amp; Metabolic Care · doi:10.1097/mco.0000000000000283 · Cited by 132 · see citing works