Comparison of regional cerebral blood flow and glucose metabolism in the normal brain: effect of aging

Co-Planar Stereotaxic Atlas of the Human Brain

Talairach, J., & Tournoux, P. (1988) · Medical Entomology and Zoology · Cited by 11,798 · see citing works

Co-planar stereotaxic atlas of the human brain

Laitinen, L. (1989) · Clinical Neurology and Neurosurgery · doi:10.1016/0303-8467(89)90128-5 · Cited by 7,565 · see citing works

Minuit - a system for function minimization and analysis of the parameter errors and correlations

James, F., & Roos, M. (1975) · Computer Physics Communications · doi:10.1016/0010-4655(75)90039-9 · Cited by 3,274 · see citing works

Synaptic density in human frontal cortex —Developmental changes and effects of aging

Peter R., H. (1979) · Brain Research · doi:10.1016/0006-8993(79)90349-4 · Cited by 2,645 · see citing works

Tomographic measurement of local cerebral glucose metabolic rate in humans with (F‐18)2‐fluoro‐2‐deoxy‐D‐glucose: Validation of method

Phelps, M. E., Huang, S. C., Hoffman, E. J., Selin, C. E., Sokoloff, L., & Kuhl, D. E. (1979) · Annals of Neurology · doi:10.1002/ana.410060502 · Cited by 2,417 · see citing works

Quantitative Measurement of Regional Cerebral Blood Flow and Oxygen Metabolism in Man Using 15O and Positron Emission Tomography

Frackowiak, R. S. J., Lenzi, G.-L., Jones, T., & Heather, J. D. (1980) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-198012000-00001 · Cited by 1,241 · see citing works

CEREBRAL BLOOD FLOW, BLOOD VOLUME AND OXYGEN UTILIZATION

Leenders, K. L., Perani, D., Lammertsma, A. A., Heather, J. D., Buckingham, P. D., Jones, T., Healy, M. J. R., GIBBS, J. M., WISE, R. J. S., Hatazawa, J., et al. (1990) · Brain · doi:10.1093/brain/113.1.27 · Cited by 1,094 · see citing works

Brain blood flow measured with intravenous H2(15)O. II. Implementation and validation.

Raichle, M. E., Martin, W. R. W., Herscovitch, P., Mintun, M. A., & Markham, J. (1983) · PubMed · Cited by 1,015 · see citing works

Neocortical cell counts in normal human adult aging

Terry, R. D., DeTeresa, R. M., & Hansen, L. A. (1987) · Annals of Neurology · doi:10.1002/ana.410210603 · Cited by 686 · see citing works

The ECAT EXACT HR

Wienhard, K., Dahlbom, M. L., Eriksson, L., Michel, C. J., Bruckbauer, T., Pietrzyk, U., & Heiss, W. (1994) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-199401000-00023 · Cited by 561 · see citing works

Dendritic Growth in the Aged Human Brain and Failure of Growth in Senile Dementia

Buell, S. J., & Coleman, P. D. (1979) · Science · doi:10.1126/science.493989 · Cited by 475 · see citing works

Quantitative synaptic alterations in the human neocortex during normal aging

Masliah, E., Mallory, M. E., Hansen, L. A., DeTeresa, R. M., & Terry, R. D. (1993) · Neurology · doi:10.1212/wnl.43.1_part_1.192 · Cited by 408 · see citing works

Cerebral Blood Flow

McHenry, L. C. (1966) · New England Journal of Medicine · doi:10.1056/nejm196601132740206 · Cited by 372 · see citing works

Progressive dendritic changes in aging human cortex

Scheibel, M. E., Lindsay, R. D., Tomiyasu, U., & Scheibel, A. B. (1975) · Experimental Neurology · doi:10.1016/0014-4886(75)90072-2 · Cited by 365 · see citing works

Effects of Human Aging on Patterns of Local Cerebral Glucose Utilization Determined by the [ ¹⁸ F] Fluorodeoxyglucose Method

Kuhl, D. E., Metter, E. J., Riege, W. H., & Phelps, M. E. (1982) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1982.15 · Cited by 338 · see citing works

Differential effects of electrical stimulation of sciatic nerve on metabolic activity in spinal cord and dorsal root ganglion in the rat.

Kadekaro, M., Crane, A. M., & Sokoloff, L. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.17.6010 · Cited by 337 · see citing works

An interactive technique for three-dimensional image registration: validation for PET, SPECT, MRI and CT brain studies.

Pietrzyk, U., Herholz, K., Fink, G. R., Jacobs, A., Mielke, R., Slansky, I., Würker, M., & Heiss, W. (1994) · PubMed · Cited by 318 · see citing works

Intercorrelations of Glucose Metabolic Rates between Brain Regions: Application to Healthy Males in a State of Reduced Sensory Input

Horwitz, B., Duara, R., & Rapoport, S. I. (1984) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1984.73 · Cited by 314 · see citing works

Human brain glucose utilization and cognitive function in relation to age

Duara, R., PhD, C. G., PhD, J. H., Ingvar, D. H., Sokoloff, L., Margolin, R. A., PhD, R. G. M., Cutler, N. R., & Рапопорт, С. И. (1984) · Annals of Neurology · doi:10.1002/ana.410160613 · Cited by 262 · see citing works

CEREBRAL GLUCOSE UTILIZATION, AS MEASURED WITH POSITRON EMISSION TOMOGRAPHY IN 21 RESTING HEALTHY MEN BETWEEN THE AGES OF 21 AND 83 YEARS

Duara, R., Margolin, R. A., Robertson‐Tchabo, E. A., London, E. D., Schwartz, M. L., Renfrew, J. W., Koziarz, B., Sundaram, M., GRADY, C., Moore, A. M., et al. (1983) · Brain · doi:10.1093/brain/106.3.761 · Cited by 228 · see citing works

Regional Kinetic Constants and Cerebral Metabolic Rate for Glucose in Normal Human Volunteers Determined by Dynamic Positron Emission Tomography of [ 18 F]-2-Fluoro-2-Deoxy-D-Glucose

Heiss, W., Pawlik, G., Herholz, K., Wagner, R. L., Göldner, H. J., & Wienhard, K. (1984) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1984.30 · Cited by 210 · see citing works

Comparative Regional Analysis of 2-Fluorodeoxyglucose and Methylglucose Uptake in Brain of Four Stroke Patients. With Special Reference to the Regional Estimation of the Lumped Constant

GJEDDE, A. H., Wienhard, K., Heiss, W., Kloster, G., Diemer, N. H., Herholz, K., & Pawlik, G. (1985) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1985.23 · Cited by 181 · see citing works

Sensitivity of Cerebral Glucose Metabolism to Age, Gender, Brain Volume, Brain Atrophy, and Cerebrovascular Risk Factors

Yoshii, F., Barker, W. W., Chang, J. Y., Loewenstein, D., Apicella, A., Smith, D. D., Boothe, T. E., Ginsberg, M. D., Pascal, S., & Duara, R. (1988) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1988.112 · Cited by 168 · see citing works

Cerebral glucose metabolic rates in normal human females versus normal males

Baxter, L. R., Mazziotta, J. C., Phelps, M. E., Selin, C. E., Guzé, B. H., & Fairbanks, L. A. (1987) · Psychiatry Research · doi:10.1016/0165-1781(87)90028-x · Cited by 165 · see citing works

The Effect of Anxiety on Cortical Cerebral Blood Flow and Metabolism

Gur, R. C., Gur, R. E., Resnick, S. M., Skolnick, B. E., Alavi, A. A., & Reivich, M. (1987) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1987.40 · Cited by 159 · see citing works

Cortical Synaptic Changes and Gliosis in Normal Aging, Alzheimer's Disease and Frontal Lobe Degeneration

Liu, X., Erikson, C., & Brun, A. E. (1996) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000106867 · Cited by 152 · see citing works

Neuroanatomy and Cranial Computed Tomography

Hj, K., & Weinrich, W. (1986) · Medical Entomology and Zoology · Cited by 140 · see citing works

Reproducibility of Cerebral Glucose Metabolic Measurements in Resting Human Subjects

Bartlett, E. J., Brodie, J. D., Wolf, A. P., Christman, D. R., LASKA, E. M., & Meissner, M. (1988) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1988.91 · Cited by 136 · see citing works

Brain Glucose Metabolism in Postanoxic Syndrome

Devolder, A. (1990) · Archives of Neurology · doi:10.1001/archneur.1990.00530020103022 · Cited by 130 · see citing works

Morphological adaptive response of the synaptic junctional zones in the human dentate gyrus during aging and Alzheimer's disease

Bertoni–Freddari, C., Fattoretti, P., Casoli, T., Meier-Ruge, W. A., & ULRICH, J. (1990) · Brain Research · doi:10.1016/0006-8993(90)91009-6 · Cited by 121 · see citing works

Brain energy metabolism in early blind subjects: neural activity in the visual cortex

Volder, A. D., Bol, A., Blin, J., Robert, A. R., Arno, P., Grandin, C. B. G., Michel, C. J., & Veraart, C. (1997) · Brain Research · doi:10.1016/s0006-8993(96)01352-2 · Cited by 121 · see citing works

Age differences in intercorrelations between regional cerebral metabolic rates for glucose

Horwitz, B., Duara, R., & Rapoport, S. I. (1986) · Annals of Neurology · doi:10.1002/ana.410190111 · Cited by 103 · see citing works

Positron Emission Tomography and Computed Tomography Assessments of the Aging Human Brain

de Leon, M. J., GEORGE, A. E., Ferris, S. H., Christman, D. R., Fowler, J. S., Gentes, C. I., Brodie, J. D., Reisberg, ‌., & Wolf, A. P. (1984) · Journal of Computer Assisted Tomography · doi:10.1097/00004728-198402000-00017 · Cited by 97 · see citing works

Intersubject variability of brain glucose metabolic measurements in young normal males.

Wang, G., Volkow, N. D., Wolf, A. P., Brodie, J. D., & HITZEMANN, R. J. (1994) · PubMed · Cited by 87 · see citing works

Kinetic Analysis of the Human Blood-Brain Barrier Transport of Lactate and its Influence by Hypercapnia

Knudsen, G. M., Paulson, O. B., & Hertz, M. M. (1991) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1991.107 · Cited by 84 · see citing works

Stability of regional cerebral glucose metabolism in the normal brain measured by positron emission tomography.

Tyler, J. L., Strother, S. C., Zatorre, R. J., Alivisatos, B., Worsley, K. J., Dikšić, M., & Yamamoto, Y. (1988) · PubMed · Cited by 80 · see citing works

Cerebral Glucose Metabolism as a Function of Age in Man: Influence of the Rate Constants in the Fluorodeoxyglucose Method

Hawkins, R. A., Mazziotta, J. C., Phelps, M. E., Huang, S., Kuhl, D. E., Carson, R. E., Metter, E. J., & Riege, W. H. (1983) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1983.34 · Cited by 77 · see citing works

Photic Stimulation Study of Changing the Arterial Partial Pressure Level of Carbon Dioxide

Shimosegawa, E., Kanno, I., Hatazawa, J., Fujita, H., Iida, H., Miura, S., Murakami, M., Inugami, A., Ogawa, T., Itoh, H., et al. (1995) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1995.12 · Cited by 75 · see citing works

Reproducibility of Resting Cerebral Blood Flow Measurements with H 2 15 O Positron Emission Tomography in Humans

Matthew, E. M., Andreason, P., Carson, R. E., Herscovitch, P., Pettigrew, K. D., Cohen, R. M., King, C., Johanson, C., & Paul, S. M. (1993) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1993.95 · Cited by 74 · see citing works

Gender differences in correlations of cerebral glucose matabolic rates in young normal adults

Azari, N. P., Рапопорт, С. И., Grady, C. L., DeCarli, C. S., Haxby, J. V., Schapiro, M. B., & Horwitz, B. (1992) · Brain Research · doi:10.1016/0006-8993(92)90817-s · Cited by 59 · see citing works

Effect of gender on glucose utilization rates in healthy humans: A positron emission tomography study

Miura, S., Schapiro, M. B., Grady, C. L., Kumar, A., Salerno, J. A., Kozachuk, W. E., Wagner, E., Рапопорт, С. И., & Horwitz, B. (1990) · Journal of Neuroscience Research · doi:10.1002/jnr.490270410 · Cited by 55 · see citing works

Reproducibility of cerebral glucose utilization measured by PET and the [18F]-2-fluoro-2-deoxy-d-glucose method in resting, healthy human subjects

Maquet, P., Dive, D., Salmon, É., von Frenckel, R., & Franck, G. (1990) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/bf00842779 · Cited by 53 · see citing works

Simulating functional interactions in the brain: A model for examining correlations between regional cerebral metabolic rates

Horwitz, B. (1990) · International Journal of Bio-Medical Computing · doi:10.1016/0020-7101(90)90039-w · Cited by 52 · see citing works

A Relationship between Metabolism in Frontal Lobes and Cerebellum in Normal Subjects Studied with PET

Junck, L., Gilman, S., Rothley, J., Betley, A. T., Koeppe, R. A., & Hichwa, R. D. (1988) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1988.132 · Cited by 51 · see citing works

Optimizing rod window width in positron emission tomography

Jones, W. F., Digby, W. M., Luk, W. K., Casey, M. E., & Byars, L. G. (1995) · IEEE Transactions on Medical Imaging · doi:10.1109/42.387708 · Cited by 51 · see citing works

Plasticity of the synaptic contact zone following loss of synapses in the cerebral cortex of aging humans

Adams, I. (1987) · Brain Research · doi:10.1016/0006-8993(87)91479-x · Cited by 44 · see citing works

Functional Interactions in the Brain: Use of Correlations between Regional Metabolic Rates

Horwitz, B. (1991) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1991.46 · Cited by 41 · see citing works

The Influence of Biological and Technical Factors on the Variability of Global and Regional Brain Metabolism of 2-[ 18 F]Fluoro-2-Deoxy-D-Glucose

Camargo, E. E., Szabó, Z. R., Links, J. M., Sostre, S., Dannals, R. F., & Wagner, H. N. (1992) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.1992.38 · Cited by 40 · see citing works

Mediman: an object oriented programming approach for medical image analysis

Coppens, A., Sibomana, M., Bol, A., & Michel, C. J. (1993) · IEEE Transactions on Nuclear Science · doi:10.1109/23.256691 · Cited by 31 · see citing works

The Lumped Constant in the Deoxyglucose Procedure Declines with Age in Fischer‐344 Rats

Takei, H., Fredericks, W. R., & Rapoport, S. I. (1986) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1986.tb13059.x · Cited by 25 · see citing works

Measurement of cerebral blood flow with a bolus of oxygen-15-labelled water: Comparison of dynamic and integral methods

Bol, A., Vanmelckenbeke, P., Michel, C. J., Cogneau, M., & Goffinet, A. M. (1990) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/bf00812363 · Cited by 24 · see citing works

Neuroanatomy and cranial computed tomography

Ball, M. R. (1987) · Surgical Neurology · doi:10.1016/0090-3019(87)90121-2 · Cited by 23 · see citing works

Interactive delineation of brain sulci and their merging into functional PET images

Michel, C. J., Sibomana, M., Bodart, J.-M., Grandin, C. B. G., Coppens, A., Bol, A., Volder, A. D., Warscotte, V., Thiran, J., & Macq, B. M. M. (2002) · IEEE Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC) · doi:10.1109/nssmic.1995.500306 · Cited by 20 · see citing works

Regional lumped constant differences and asymmetry in fluorine-18-FDG uptake in temporal lobe epilepsy.

Reutens, D. C., GJEDDE, A. H., & Meyer, E. (1998) · PubMed · Cited by 15 · see citing works

The FDG model and its application in clinical PET studies

Wienhard, K. (1992) · Springer eBooks · doi:10.1007/978-3-7091-9209-2_4 · Cited by 9 · see citing works

Pathophysiology of Sleep Apnea

Dempsey, J. A., Veasey, S. C., Morgan, B. J., & O'Donnell, C. P. (2010) · Physiological Reviews · doi:10.1152/physrev.00043.2008 · Cited by 2,243 · see citing works

Alterations in the BOLD fMRI signal with ageing and disease: a challenge for neuroimaging

D’Esposito, M., Deouell, L. Y., & Gazzaley, A. H. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1246 · Cited by 852 · see citing works

Aging, sexual dimorphism, and hemispheric asymmetry of the cerebral cortex: replicability of regional differences in volume

Raz, N., Gunning‐Dixon, F. M., Head, D. M., Rodrigue, K. M., Williamson, A. L., & Acker, J. D. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(03)00118-0 · Cited by 715 · see citing works

Differential vulnerability of anterior white matter in nondemented aging with minimal acceleration in dementia of the Alzheimer type: Evidence from diffusion tensor imaging.

Head, D. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh003 · Cited by 645 · see citing works

Brain fuel metabolism, aging, and Alzheimer’s disease

Cunnane, S. C., Nugent, S., Roy, M., Courchesne‐Loyer, A., Croteau, É., Tremblay, S., Castellano, A., Pifferi, F., Bocti, C., Paquet, N., et al. (2010) · Nutrition · doi:10.1016/j.nut.2010.07.021 · Cited by 607 · see citing works

Elevated gene expression levels distinguish human from non-human primate brains

Cáceres, M., Lachuer, J., Zapala, M. A., Redmond, J. C., Kudo, L., Geschwind, D. H., Lockhart, D. J., Preuss, T. M., & Barlow, C. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2135499100 · Cited by 491 · see citing works

Normal cerebral perfusion measurements using arterial spin labeling: Reproducibility, stability, and age and gender effects

Parkes, L. M., Rashid, W., Chard, D., & Tofts, P. S. (2004) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20023 · Cited by 450 · see citing works

Cardiovascular Risk Factors Promote Brain Hypoperfusion Leading to Cognitive Decline and Dementia

de la Torre, J. C. (2012) · Cardiovascular Psychiatry and Neurology · doi:10.1155/2012/367516 · Cited by 442 · see citing works

Cellular metabolic and autophagic pathways: Traffic control by redox signaling

Dodson, M. B., Darley-Usmar, V. M., & Zhang, J. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.05.014 · Cited by 325 · see citing works

The microvascular frontal-subcortical syndrome of aging

Pugh, K. R. (2002) · Neurobiology of Aging · doi:10.1016/s0197-4580(01)00319-0 · Cited by 229 · see citing works

Microvascular plasticity in aging

Riddle, D. R., Sonntag, W. E., & Lichtenwalner, R. J. (2003) · Ageing Research Reviews · doi:10.1016/s1568-1637(02)00064-8 · Cited by 222 · see citing works

Effects of aging on cerebral blood flow, oxygen metabolism, and blood oxygenation level dependent responses to visual stimulation

Ances, B. M., Liang, C. L., Leontiev, O., Perthen, J. E., Fleisher, A., Lansing, A. E., & Buxton, R. B. (2008) · Human Brain Mapping · doi:10.1002/hbm.20574 · Cited by 216 · see citing works

Hormonal and Metabolic Changes of Aging and the Influence of Lifestyle Modifications

Pataky, M. W., Young, W. F., & Nair, K. S. (2021) · Mayo Clinic Proceedings · doi:10.1016/j.mayocp.2020.07.033 · Cited by 207 · see citing works

Central Sleep Apnea

Javaheri, S., & Dempsey, J. A. (2012) · Comprehensive physiology · doi:10.1002/cphy.c110057 · Cited by 227 · see citing works

The cerebellum ages slowly according to the epigenetic clock

Horvath, S., Mah, V., Lu, A. T., Woo, J. S., Choi, O.-W., Jasinska, A. J., Riancho, J. A., Tung, S., Coles, N. S., Braun, J., et al. (2015) · Aging · doi:10.18632/aging.100742 · Cited by 191 · see citing works

Aging and Gene Expression in the Primate Brain

Fraser, H. B., Khaitovich, P., Plotkin, J. B., Pääbo, S., & Eisen, M. B. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030274 · Cited by 172 · see citing works

Untitled work

Berti (2014) · doi:10.1016/j.cpet.2013.10.006 · Cited by 152 · see citing works

Dietary supplementation with medium-chain TAG has long-lasting cognition-enhancing effects in aged dogs

Pan, Y., Larson, B. T., Araujo, J. A., Lau, W. A. K., de Rivera, C., Santana, R., Gore, A. M., & Milgram, N. W. (2010) · British Journal Of Nutrition · doi:10.1017/s0007114510000097 · Cited by 144 · see citing works

A cognitive training intervention increases resting cerebral blood flow in healthy older adults

Mozolic, J. L. (2010) · Frontiers in Human Neuroscience · doi:10.3389/neuro.09.016.2010 · Cited by 142 · see citing works

Aging-Induced Dysregulation of Dicer1-Dependent MicroRNA Expression Impairs Angiogenic Capacity of Rat Cerebromicrovascular Endothelial Cells

Ungvari, Z. I., Tucsek, Z., Sosnowska, D., Toth, P. P., Gautam, T., Podlutsky, A. J., Csiszár, A., Losonczy, G., Valcarcel‐Ares, M. N., Sonntag, W. E., et al. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls242 · Cited by 139 · see citing works

Nicotinamide mononucleotide (NMN) treatment attenuates oxidative stress and rescues angiogenic capacity in aged cerebromicrovascular endothelial cells: a potential mechanism for the prevention of vascular cognitive impairment

Kiss, T., Balasubramanian, P., Valcarcel‐Ares, M. N., Tarantini, S., Yabluchanskiy, A., Csípő, T., Lipécz, Á., Reglődi, D., Zhang, X. A., Bari, F., et al. (2019) · GeroScience · doi:10.1007/s11357-019-00074-2 · Cited by 134 · see citing works

The Val66Met polymorphism of the brain-derived neurotrophic factor gene affects age-related brain morphology

Nemoto, K., Ohnishi, T., Mori, T., Moriguchi, Y., Hashimoto, R., Asada, T., & Kunugi, H. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2005.11.067 · Cited by 131 · see citing works

Resistance, vulnerability and resilience: A review of the cognitive cerebellum in aging and neurodegenerative diseases

Liang, K. J., & Carlson, E. S. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.01.004 · Cited by 131 · see citing works

Cerebral Blood Flow Measurements in Adults: A Review on the Effects of Dietary Factors and Exercise

Joris, P. J., Mensink, R. P., Adam, T. C., & Liu, T. T. (2018) · Nutrients · doi:10.3390/nu10050530 · Cited by 126 · see citing works

Resting hippocampal blood flow, spatial memory and aging

Heo, S., Prakash, R. S., Voss, M. W., Erickson, K. I., Ouyang, C., Sutton, B. P., & Kramer, A. F. (2009) · Brain Research · doi:10.1016/j.brainres.2009.12.020 · Cited by 126 · see citing works

Interaction of Age and APOE Genotype on Cerebral Blood Flow at Rest

Wierenga, C. E., Clark, L. R., Dev, S. I., Shin, D. D., Jurick, S. M., Rissman, R. A., Liu, T. T., & Bondi, M. W. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-121897 · Cited by 119 · see citing works

Decreased functional magnetic resonance imaging activity in the hippocampus in favor of the caudate nucleus in older adults tested in a virtual navigation task

Konishi, K., Etchamendy, N., Roy, S., Marighetto, A., Rajah, M. N., & Bohbot, V. D. (2013) · Hippocampus · doi:10.1002/hipo.22181 · Cited by 118 · see citing works

Cerebral blood flow and BOLD responses to a memory encoding task: A comparison between healthy young and elderly adults

Restom, K., Bangen, K. J., Bondi, M. W., Perthen, J. E., & Liu, T. T. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.05.024 · Cited by 113 · see citing works

β-amyloid and tau drive early Alzheimer’s disease decline while glucose hypometabolism drives late decline

Hammond, T. C., Xing, X., Wang, C., Ma, D., Nho, K. T., Crane, P. K., Elahi, F. M., Ziegler, D. A., Liang, G., Cheng, Q. S., et al. (2020) · Communications Biology · doi:10.1038/s42003-020-1079-x · Cited by 113 · see citing works

Compromised microvascular oxygen delivery increases brain tissue vulnerability with age

Moeini, M., Lu, X., Avti, P., Damseh, R., Bélanger, S., Picard, F., Boas, D. A., Kakkar, A. K., & Lesage, F. (2018) · Scientific Reports · doi:10.1038/s41598-018-26543-w · Cited by 109 · see citing works

Human brain evolution: From gene discovery to phenotype discovery

Preuss, T. M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1201894109 · Cited by 108 · see citing works

Brain FDG PET study of normal aging in Japanese: effect of atrophy correction

Yanase, D., Matsunari, I., Yajima, K., Chen, W., Fujikawa, A., Nishimura, S., Matsuda, H., & Yamada, M. (2005) · European Journal of Nuclear Medicine and Molecular Imaging · doi:10.1007/s00259-005-1767-2 · Cited by 104 · see citing works

Functional activation imaging in aging and dementia

Prvulovic, D., van de Ven, V. G., Sack, A. T., Maurer, K., & Linden, D. E. J. (2005) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2005.06.006 · Cited by 103 · see citing works

Use of Functional Magnetic Resonance Imaging in the Early Identification of Alzheimer's Disease

Wierenga, C. E., & Bondi, M. W. (2007) · Neuropsychology Review · doi:10.1007/s11065-007-9025-y · Cited by 102 · see citing works

CORRELATION BETWEEN INHIBITION, WORKING MEMORY AND DELIMITED FRONTAL AREA BLOOD FLOW MEASURED BY 99mTc-BICISATE SPECT IN ALCOHOL-DEPENDENT PATIENTS

Noël, X. (2001) · Alcohol and Alcoholism · doi:10.1093/alcalc/36.6.556 · Cited by 98 · see citing works

Circulating IGF-1 deficiency exacerbates hypertension-induced microvascular rarefaction in the mouse hippocampus and retrosplenial cortex: implications for cerebromicrovascular and brain aging

Tarantini, S., Tucsek, Z., Valcarcel-Ares, M. N., Toth, P., Gautam, T., Giles, C. B., Ballabh, P., Wei, J. Y., Wren, J. D., Ashpole, N. M., et al. (2016) · AGE · doi:10.1007/s11357-016-9931-0 · Cited by 98 · see citing works

Transcranial laser stimulation: Mitochondrial and cerebrovascular effects in younger and older healthy adults

Saucedo, C. L., Courtois, E. C., Wade, Z. S., Kelley, M. N., Kheradbin, N., Barrett, D. W., & Gonzalez-Lima, F. (2021) · Brain stimulation · doi:10.1016/j.brs.2021.02.011 · Cited by 99 · see citing works

Functional Genomics of Brain Aging and Alzheimers Disease: Focus on Selective Neuronal Vulnerability

Wang, X., Michaelis, M. L., & Michaelis, E. K. (2010) · Current Genomics · doi:10.2174/138920210793360943 · Cited by 93 · see citing works

An arteriolar compliance model of the cerebral blood flow response to neural stimulus

Behzadi, Y., & Liu, T. T. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2004.12.057 · Cited by 92 · see citing works

Caloric restriction increases ketone bodies metabolism and preserves blood flow in aging brain

Lin, A.-L., Zhang, W., Gao, X., & Watts, L. (2015) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.03.012 · Cited by 90 · see citing works

Positron Emission Tomography Examination of Cerebral Blood Flow and Glucose Metabolism in Young CADASIL Patients

Tuominen, S., Miao, Q., Kurki, T. J. I., Tuisku, S., Pöyhönen, M., Kalimo, H., Viitanen, M. H., Sipilä, H. T., Bergman, J. R., & Rinne, J. O. (2004) · Stroke · doi:10.1161/01.str.0000124124.69842.2d · Cited by 89 · see citing works

Efficacy of a Therapeutic Diet on Dogs With Signs of Cognitive Dysfunction Syndrome (CDS): A Prospective Double Blinded Placebo Controlled Clinical Study

Pan, Y., Landsberg, G. M., Mougeot, I., Kelly, S., Xu, H., Bhatnagar, S., Gardner, C. L., & Milgram, N. W. (2018) · Frontiers in Nutrition · doi:10.3389/fnut.2018.00127 · Cited by 83 · see citing works

A longitudinal characterization of perfusion in the aging brain and associations with cognition and neural structure

Staffaroni, A. M., Cobigo, Y., Elahi, F. M., Casaletto, K. B., Walters, S. M., Wolf, A. A., Lindbergh, C. A., Rosen, H. J., & Kramer, J. H. (2019) · Human Brain Mapping · doi:10.1002/hbm.24613 · Cited by 81 · see citing works

Increasing measurement accuracy of age-related BOLD signal change: Minimizing vascular contributions by resting-state-fluctuation-of-amplitude scaling

Kannurpatti, S. S., Motes, M. A., Rypma, B., & Biswal, B. B. (2010) · Human Brain Mapping · doi:10.1002/hbm.21097 · Cited by 83 · see citing works

Scaling of Brain Metabolism and Blood Flow in Relation to Capillary and Neural Scaling

Karbowski, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0026709 · Cited by 86 · see citing works

Caloric restriction preserves memory and reduces anxiety of aging mice with early enhancement of neurovascular functions

Parikh, I. J., Guo, J., Chuang, K., Zhong, Y., Rempe, R. G., Hoffman, J. D., Armstrong, R., Bauer, B., Hartz, A. M. S., & Lin, A. (2016) · Aging · doi:10.18632/aging.101094 · Cited by 82 · see citing works

Dietary medium chain triglycerides for management of epilepsy: New data from human, dog, and rodent studies

Han, F. Y., Conboy-Schmidt, L., Quist‐Rybachuk, G., Volk, H. A., Zanghi, B. M., Pan, Y., & Borges, K. (2021) · Epilepsia · doi:10.1111/epi.16972 · Cited by 76 · see citing works

A longitudinal study of oculomotor function in normal older people

Kerber, K. A., Ishiyama, G. P., & Baloh, R. W. (2005) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.07.009 · Cited by 72 · see citing works

Age-related cognitive decline: Can neural stem cells help us?

Artegiani, B., & Calegari, F. (2012) · Aging · doi:10.18632/aging.100446 · Cited by 70 · see citing works

Impaired Cerebrovascular Function in Coronary Artery Disease Patients and Recovery Following Cardiac Rehabilitation

Anazodo, U., Shoemaker, J. K., Suskin, N., Ssali, T., Wang, D. J. J., & Lawrence, K. S. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2015.00224 · Cited by 68 · see citing works

A Systematic Review of the Application of Functional Near-Infrared Spectroscopy to the Study of Cerebral Hemodynamics in Healthy Aging

Yeung, M. K.-C., & Chan, A. S.-Y. (2020) · Neuropsychology Review · doi:10.1007/s11065-020-09455-3 · Cited by 67 · see citing works

Long‐term mild‐intensity exercise regimen preserves prefrontal cortical volume against aging

Tamura, M., Nemoto, K., Kawaguchi, A., Kato, M., Arai, T., Kakuma, T., Mizukami, K., Matsuda, H., Soya, H., & Asada, T. (2014) · International Journal of Geriatric Psychiatry · doi:10.1002/gps.4205 · Cited by 67 · see citing works

Quantification of the Biological Age of the Brain Using Neuroimaging

Cole, J. H., Franke, K., & Cherbuin, N. (2019) · Healthy ageing and longevity · doi:10.1007/978-3-030-24970-0_19 · Cited by 64 · see citing works

An investigation of cerebral oxygen utilization, blood flow and cognition in healthy aging

Catchlove, S. J., Macpherson, H., Hughes, M. E., Chen, Y. J., Parrish, T. B., & Pipingas, A. (2018) · PLoS ONE · doi:10.1371/journal.pone.0197055 · Cited by 62 · see citing works

The Age-Related Perfusion Pattern Measured With Arterial Spin Labeling MRI in Healthy Subjects

Zhang, N., Gordon, M., Ma, Y.-L., Chi, B., Gomar, J., Peng, S., Kingsley, P., Eidelberg, D., & Goldberg, T. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00214 · Cited by 67 · see citing works

Transitions in metabolic and immune systems from pre-menopause to post-menopause: implications for age-associated neurodegenerative diseases

Wang, Y., Mishra, A., & Brinton, R. D. (2020) · F1000Research · doi:10.12688/f1000research.21599.1 · Cited by 63 · see citing works

Enhancing Cognitive Function across the Life Span

Korol, D. L. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb02091.x · Cited by 62 · see citing works

Functional Magnetic Resonance Imaging of Compensatory Neural Recruitment in Aging and Risk for Alzheimer’s Disease: Review and Recommendations

Han, S. D., Bangen, K. J., & Bondi, M. W. (2008) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000182420 · Cited by 60 · see citing works

Multimodal Imaging in Rats Reveals Impaired Neurovascular Coupling in Sustained Hypertension

Calcinaghi, N., Wyss, M. T., Jolivet, R., Singh, A., Keller, A. L., Winnik, S. H., Fritschy, J., Buck, A., Matter, C. M., & Weber, B. (2013) · Stroke · doi:10.1161/strokeaha.111.000185 · Cited by 60 · see citing works

Regional Differences in the Coupling between Resting Cerebral Blood Flow and Metabolism may Indicate Action Preparedness as a Default State

Gur, R., Ragland, J., Reivich, M., Greenberg, J., Alavi, A., & Gur, R. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn087 · Cited by 57 · see citing works

Regional Correlation between Resting State FDG PET and pCASL Perfusion MRI

Cha, Y.-H. K., Jog, M., Kim, Y., Chakrapani, S., Kraman, S. M., & Wang, D. J. J. (2013) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2013.147 · Cited by 58 · see citing works

A million persons, a million dreams: a vision for a national center of radiation epidemiology and biology

Boice, J. D., Quinn, B. M., Al‐Nabulsi, I., Ansari, A. J., Blake, P. K., Blattnig, S. R., Caffrey, E., Cohen, S. S., Golden, A. P., Held, K. D., et al. (2021) · International Journal of Radiation Biology · doi:10.1080/09553002.2021.1988183 · Cited by 49 · see citing works

Effects of vinpocetine on the redistribution of cerebral blood flow and glucose metabolism in chronic ischemic stroke patients: a PET study

Szilágyi, G., Nagy, Z., Balkay, L., Boros, I., Emri, M., Lehel, S., Márián, T., Molnár, T., Szakáll, S., Trón, L., et al. (2005) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2004.11.053 · Cited by 49 · see citing works

Electroconvulsive therapy changes the regional resting state function measured by regional homogeneity (ReHo) and amplitude of low frequency fluctuations (ALFF) in elderly major depressive disorder patients: An exploratory study

Kong, X., Xu, S., Sun, Y., Wang, K., Wang, C., Zhang, J., Xia, J.-X., Zhang, L., Tan, B.-J., & Xie, X. (2017) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2017.04.001 · Cited by 44 · see citing works

Immediate effects of a single session of physical exercise on cognition and cerebral blood flow: A randomized controlled study of older adults

Olivo, G., Nilsson, J., Garzón, B., Lebedev, A. V., Wåhlin, A., Tarassova, O., Ekblom, M., & Lövdén, M. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2020.117500 · Cited by 43 · see citing works

Early metabolic crisis-related brain atrophy and cognition in traumatic brain injury

Wright, M., McArthur, D. L., Alger, J. R., Horn, J. V., Andrei Irimia, A., Filippou-Frye, M., Glenn, T. C., Hovda, D. A., & Vespa, P. M. (2013) · Brain Imaging and Behavior · doi:10.1007/s11682-013-9231-6 · Cited by 44 · see citing works

Comparison of FDG-PET and IMP-SPECT in patients with dementia with Lewy bodies

Ishii, K., Hosaka, K., Mori, T., & Mori, E. (2004) · Annals of Nuclear Medicine · doi:10.1007/bf02984489 · Cited by 44 · see citing works

Longitudinal evaluation of surrogates of regional cerebral blood flow computed from dynamic amyloid PET imaging

Bilgel, M., Beason‐Held, L. L., An, Y., Zhou, Y., Wong, D. F., & Resnick, S. M. (2019) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x19830537 · Cited by 42 · see citing works

Cerebral Hemodynamics in the Elderly

Yang, D., Cabral, D., Gaspard, E. N., Lipton, R. B., Rundek, T., & Derby, C. A. (2016) · Journal of Ultrasound in Medicine · doi:10.7863/ultra.15.10040 · Cited by 41 · see citing works

Coupling of cerebral blood flow and functional connectivity is decreased in healthy aging

Galiano, A., Mengual, E., de Eulate, M. R. G., Galdeano, I., Vidorreta, M., Recio, M., Riverol, M., Zubieta, J. L., & Fernández‐Seara, M. A. (2019) · Brain Imaging and Behavior · doi:10.1007/s11682-019-00157-w · Cited by 39 · see citing works

Polyphenols as an Effective Therapeutic Intervention Against Cognitive Decline During Normal and Pathological Brain Aging

Devi, S. A., & Chamoli, A. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-42667-5_7 · Cited by 41 · see citing works

Glucose tolerance during moderate alcohol intake: insights on insulin action from glucose/lactate dynamics.

Avogaro, A., Watanabe, R., Gottardo, L., de Kreutzenberg, S., Tiengo, A., & Pacini, G. (2002) · Journal of Clinical Endocrinology and Metabolism · doi:10.1210/jcem.87.3.8347 · Cited by 44 · see citing works

Polyphenols and brain health

Vauzour, D. (2017) · OCL · doi:10.1051/ocl/2017008 · Cited by 43 · see citing works

Intrinsic Brain Connectivity Related to Age in Young and Middle Aged Adults

Hampson, M., Tokoglu, F., Shen, X., Scheinost, D., Papademetris, X., & Constable, R. T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044067 · Cited by 39 · see citing works

Striatal size, glucose metabolic rate, and verbal learning in normal aging

Brickman, A. M., Buchsbaum, M. S., Shihabuddin, L., Hazlett, E. A., Borod, J. C., & Mohs, R. C. (2003) · Cognitive Brain Research · doi:10.1016/s0926-6410(03)00085-5 · Cited by 38 · see citing works

Neuropsychological picture of 33 spinocerebellar ataxia cases

Orsi, L., D’Agata, F., Caroppo, P., Franco, A., Caglio, M., Avidano, F., Manzone, C., & Mortara, P. (2011) · Journal of Clinical and Experimental Neuropsychology · doi:10.1080/13803395.2010.518139 · Cited by 37 · see citing works

Basal and hypercapnia-altered cerebrovascular perfusion predict mild cognitive impairment in aging rodents

Mitschelen, M. C., Garteiser, P., Carnes, B. A., Farley, J. A., Doblas, S., DeMoe, J. H., Warrington, J. P., Yan, H., Nicolle, M. M., Towner, R. A., et al. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.08.070 · Cited by 36 · see citing works

Perfusion shift from white to gray matter may account for processing speed deficits in schizophrenia

Wright, S. N., Hong, L. E., Winkler, A. M., Chiappelli, J., Nugent, K. L., Muellerklein, F., Du, X., Rowland, L. M., Wang, D. J. J., & Kochunov, P. V. (2015) · Human Brain Mapping · doi:10.1002/hbm.22878 · Cited by 35 · see citing works

The Use of Heptamethine Cyanine Dyes as Drug-Conjugate Systems in the Treatment of Primary and Metastatic Brain Tumors

Cooper, E. A., Choi, P. J., Denny, W. A., Jose, J., Dragunow, M., & Park, T. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.654921 · Cited by 35 · see citing works

A Potential Role for Glucose Transporters in the Evolution of Human Brain Size

Fedrigo, O. D., Pfefferle, A. D., Babbitt, C. C., Haygood, R., Wall, C. E., & Wray, G. A. (2011) · Brain Behavior and Evolution · doi:10.1159/000329852 · Cited by 35 · see citing works

Endothelial deficiency of insulin‐like growth factor‐1 receptor leads to blood–brain barrier disruption and accelerated endothelial senescence in mice, mimicking aspects of the brain aging phenotype

Gulej, R., Csík, B., Faakye, J., Tarantini, S., Shanmugarama, S., Chandragiri, S. S., Mukli, P., Conley, S. M., Csiszár, A., Ungvari, Z. I., et al. (2023) · Microcirculation · doi:10.1111/micc.12840 · Cited by 32 · see citing works

Links Between Metabolic and Structural Changes in the Brain of Cognitively Normal Older Adults: A 4-Year Longitudinal Follow-Up

Castellano, C., Hudon, C., Croteau, É., Fortier, M., St‐Pierre, V., Vandenberghe, C., Nugent, S., Tremblay, S., Paquet, N., Lepage, M., et al. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00015 · Cited by 32 · see citing works

Feasibility of simultaneous whole-brain imaging on an integrated PET-MRI system using an enhanced 2-point Dixon attenuation correction method

Anazodo, U., Thiessen, J. D., Ssali, T., Mandel, J., nther, M. G. ⁄., Butler, J., Pavlosky, W. F., Prato, F. S., Thompson, R. T., & Lawrence, K. S. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00434 · Cited by 31 · see citing works

Cerebral hemodynamic and oxygenation changes induced by inner and heard speech: a study combining functional near-infrared spectroscopy and capnography

Scholkmann, F., Klein, S. D., Gerber, U., Wolf, M., & Wolf, U. (2014) · Journal of Biomedical Optics · doi:10.1117/1.jbo.19.1.017002 · Cited by 31 · see citing works

On the time course of attentional focusing in older adults

Jefferies, L. N., Roggeveen, A. B., Enns, J. T., Bennett, P., Sekuler, A. B., & Lollo, V. D. (2013) · Psychological Research · doi:10.1007/s00426-013-0528-2 · Cited by 29 · see citing works

Impairments in Brain Bioenergetics in Aging and Tau Pathology: A Chicken and Egg Situation?

Grimm, A. (2021) · Cells · doi:10.3390/cells10102531 · Cited by 28 · see citing works

Resting cerebral glucose metabolism and perfusion patterns in women with posttraumatic stress disorder related to sexual assault

Kim, S.-Y., Chung, Y. K., Kim, B. S., Lee, S. J., Yoon, J., & An, Y. (2012) · Psychiatry Research Neuroimaging · doi:10.1016/j.pscychresns.2011.08.007 · Cited by 28 · see citing works

Brain perfusion imaging in amyotrophic lateral sclerosis: Extent of cortical changes according to the severity and topography of motor impairment

Habert, M., Lacomblez, L., Maksud, P., Fakhri, G. E., Pradat, J., & Meininger, V. (2007) · Amyotrophic Lateral Sclerosis · doi:10.1080/14660820601048815 · Cited by 28 · see citing works

Central Sleep Apnea

Javaheri, S., & Dempsey, J. A. (2013) · Comprehensive physiology · doi:10.1002/j.2040-4603.2013.tb00482.x · Cited by 28 · see citing works

Cerebrovascular hemodynamic correlates of aging in the Lou/c rat: A model of healthy aging

Dubeau, S., Ferland, G., Gaudreau, P., Beaumont, É., & Lesage, F. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.076 · Cited by 27 · see citing works

Age-Related Increase in Cross-Sensory Noise in Resting and Steady-State Cerebral Perfusion

Hugenschmidt, C. E., Mozolic, J. L., Tan, H., Kraft, R., & Laurienti, P. J. (2009) · Brain Topography · doi:10.1007/s10548-009-0098-1 · Cited by 27 · see citing works

Scaling of cerebral blood perfusion in primates and marsupials

Seymour, R. S., Angove, S. E., Snelling, E. P., & Cassey, P. (2015) · Journal of Experimental Biology · doi:10.1242/jeb.124826 · Cited by 26 · see citing works

Diverging roles of the anterior insula in trauma-exposed individuals vulnerable or resilient to posttraumatic stress disorder

Jeong, H. S., Chung, Y., Ma, J., Kim, J., Hong, G., Oh, J. K., Kim, M., Ha, E., Hong, H., Yoon, S. J., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-51727-3 · Cited by 27 · see citing works

Empirical derivation of the reference region for computing diagnostic sensitive 18fluorodeoxyglucose ratios in Alzheimer's disease based on the ADNI sample

Rasmussen, J. M., Lakatos, A., van Erp, T. G. M., Kruggel, F., Keator, D. B., Fallon, J., Macciardi, F. M., & Potkin, S. G. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.09.008 · Cited by 26 · see citing works

A statistical investigation of normal regional intra-subject heterogeneity of brain metabolism and perfusion by F-18 FDG and O-15 H2O PET imaging

Wong, C.-Y. O., Thie, J. A., Gaskill, M., Ponto, R. A., Hill, J., Tian, H.-Y., Balon, H. R., Wu, D., FINK-BENNETT, D. M., & Nagle, C. E. (2006) · BMC Nuclear Medicine · doi:10.1186/1471-2385-6-4 · Cited by 26 · see citing works

Aging is not equal across memory systems

Gardner, R. S., Newman, L. A., Mohler, E. G., Tunur, T., Gold, P. E., & Korol, D. L. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107232 · Cited by 24 · see citing works

Nutrients, Cognitive Function, and Brain Aging: What We Have Learned from Dogs

Pan, Y.-L. (2021) · Medical Science · doi:10.3390/medsci9040072 · Cited by 22 · see citing works

The association of regional cerebral blood flow and glucose metabolism in normative ageing and insulin resistance

Deery, H. A., Liang, E. X., Paolo, R. D., Voigt, K., Murray, G., Siddiqui, M. N., Egan, G. F., Moran, C., & Jamadar, S. D. (2024) · Scientific Reports · doi:10.1038/s41598-024-65396-4 · Cited by 23 · see citing works

Kinetic modeling of PET data without blood sampling

Bentourkia, M. (2005) · IEEE Transactions on Nuclear Science · doi:10.1109/tns.2005.851442 · Cited by 23 · see citing works

Changes in diffusion path length with old age in diffuse optical tomography

Bonnéry, C., Desjardins, M., Pouliot, P., Lesage, F., Leclerc, P.-O., Hoge, R. D., & Bherer, L. (2012) · Journal of Biomedical Optics · doi:10.1117/1.jbo.17.5.056002 · Cited by 21 · see citing works

Brain Metabolism and Blood Flow During Development and Aging of the Fischer-344 Rat

Рапопорт, С. И., London, E. D., & Takei, H. (1982) · Experimental brain research. Supplementum · doi:10.1007/978-3-642-68507-1_12 · Cited by 21 · see citing works

Cerebral blood flow, cerebral oxygen metabolism, and atrophy in healthy aging

Vafaee, M. S., Borghammer, P., Aanerud, J., Cumming, P. D., & GJEDDE, A. H. (2007) · Scopus (Elsevier)

Reduction in regional cerebral metabolic rate of oxygen during human aging.

Yamaguchi, T., Kanno, I., Uemura, K., Shishido, F., Inugami, A., Ogawa, T., Murakami, M. T., & Suzuki, K. (1986) · Stroke · doi:10.1161/01.str.17.6.1220 · Cited by 260 · see citing works

Alterations in Cerebral Metabolic Rate and Blood Supply across the Adult Lifespan

Lu, H., Xu, F., Rodrigue, K. M., Kennedy, K. M., Cheng, Y., Flicker, B., Hebrank, A. C., Uh, J., & Park, D. C. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq224 · Cited by 400 · see citing works

Reduction in regional cerebral blood flow during normal aging in man.

Melamed, E., LAVY, S., Shlomo Bentin, A., Cooper, G., & Rinot, Y. (1980) · Stroke · doi:10.1161/01.str.11.1.31 · Cited by 274 · see citing works