Increased serum IgA and IgM against LPS of enterobacteria in chronic fatigue syndrome (CFS): Indication for the involvement of gram-negative enterobacteria in the etiology of CFS and for the presence of an increased gut–intestinal permeability

The Chronic Fatigue Syndrome: A Comprehensive Approach to Its Definition and Study

Fukuda, K., Straus, S. E., Hickie, I., Sharpe, M. C., Dobbins, J. G., Komaroff, A., & and International Chronic Fatigue Syndrome Study Group. (1994) · Annals of Internal Medicine · doi:10.7326/0003-4819-121-12-199412150-00009 · Cited by 4,969 · cited 1× · see citing works

Oxidative stress levels are raised in chronic fatigue syndrome and are associated with clinical symptoms

Kennedy, G., Spence, V. A., McLaren, M., Hill, A., Underwood, C., & Belch, J. J. F. (2005) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2005.04.020 · Cited by 325 · see citing works

Environmental stress–induced gastrointestinal permeability is mediated by endogenous glucocorticoids in the rat

Meddings, J. B., & Swain, M. G. (2000) · Gastroenterology · doi:10.1053/gast.2000.18152 · Cited by 269 · see citing works

Autoimmunity due to molecular mimicry as a cause of neurological disease

Levin, M. C., Lee, S. M., Kalume, F. K., Morcos, Y., Dohan, F. C., Hasty, K. A., Callaway, J. C., Zunt, J. R., Desiderio, D. M., & Stuart, J. M. (2002) · Nature Medicine · doi:10.1038/nm0502-509 · Cited by 265 · see citing works

IL-6 is essential for development of gut barrier dysfunction after hemorrhagic shock and resuscitation in mice

Yang, R., Han, X., Uchiyama, T., Watkins, S. C., Yaguchi, A., Delude, R. L., & Fink, M. P. (2003) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00177.2003 · Cited by 186 · see citing works

A rating scale for fibromyalgia and chronic fatigue syndrome (the FibroFatigue scale)

Zachrisson, O., Regland, B., Jahreskog, M., Kron, M., & Gottfries, C. G. (2002) · Journal of Psychosomatic Research · doi:10.1016/s0022-3999(01)00315-4 · Cited by 174 · see citing works

Relationship between musculoskeletal symptoms and blood markers of oxidative stress in patients with chronic fatigue syndrome

Vecchiet, J., Cipollone, F., Falasca, K., Mezzetti, A., Pizzigallo, E., Bucciarelli, T., Laurentis, S. D., Affaitati, G., Cesare, D. D., & Giamberardino, M. A. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(02)01058-3 · Cited by 142 · see citing works

Increased gut permeability after multiple trauma

Pape, H., Dwenger, A., Regel, G., et al. (1994) · British journal of surgery · doi:10.1002/bjs.1800810619 · Cited by 129 · see citing works

B1 Cells Contribute to Serum IgM, But Not to Intestinal IgA, Production in Gnotobiotic Ig Allotype Chimeric Mice

Thurnheer, M. C., Zuercher, A. W., Cebra, J. J., & Bos, N. A. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.9.4564 · Cited by 117 · see citing works

Hepatic steatosis and type 2 diabetes mellitus

Clark, J. M., & Diehl, A. M. (2002) · Current Diabetes Reports · doi:10.1007/s11892-002-0085-3 · Cited by 106 · see citing works

Measurement of intestinal permeability to mannitol and lactulose as a means of diagnosing food allergy and evaluating therapeutic effectiveness of disodium cromoglycate.

Andre, C., Andre, F., Colin, L., et al. (1987) · PubMed · Cited by 79 · see citing works

Lower serum zinc in Chronic Fatigue Syndrome (CFS): Relationships to immune dysfunctions and relevance for the oxidative stress status in CFS

Maes, M. H. J., Mihaylova, I., & Ruyter, M. D. (2005) · Journal of Affective Disorders · doi:10.1016/j.jad.2005.11.002 · Cited by 77 · see citing works

Glutamine supplemented parenteral nutrition prevents intestinal ischemia- reperfusion injury in rats

Wu, G. (2004) · World Journal of Gastroenterology · doi:10.3748/wjg.v10.i17.2592 · Cited by 57 · see citing works

Bronchodilators in Bronchoscopy-Induced Airflow Limitation in Allergen-Sensitized Cats

Kirschvink, N. A., Leemans, J., Delvaux, F. H., et al. (2005) · Journal of Veterinary Internal Medicine · doi:10.1892/0891-6640(2005)19 · Cited by 46 · see citing works

Sustained Strenuous Exercise Increases Intestinal Permeability in Racing Alaskan Sled Dogs

Davis, M. S., Willard, M. D., Williamson, K., et al. (2005) · Journal of Veterinary Internal Medicine · doi:10.1111/j.1939-1676.2005.tb02655.x · Cited by 37 · see citing works

Decreased dehydroepiandrosterone sulfate but normal insulin-like growth factor in chronic fatigue syndrome (CFS): relevance for the inflammatory response in CFS.

Maes, M. H. J., Mihaylova, I., & Ruyter, M. D. (2005) · PubMed · Cited by 27 · see citing works

Intérêt de l'évaluation d'IgM et d'IgA spécifiques circulant dans le serum de malades atteints de sclérose en plaques (SEP)

Geffard, M., Bodet, D., Martinet, Y., & Dabadie, M. P. (2002) · Immuno-analyse & Biologie Spécialisée · doi:10.1016/s0923-2532(02)01214-0 · Cited by 27 · see citing works

The Gut Microbiome and the Brain

Galland, L. (2014) · Journal of Medicinal Food · doi:10.1089/jmf.2014.7000 · Cited by 648 · see citing works

Role of the Toll Like receptor (TLR) radical cycle in chronic inflammation: Possible treatments targeting the TLR4 pathway

Lucas, K., & Maes, M. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8425-7 · Cited by 466 · see citing works

Increased IgA and IgM responses against gut commensals in chronic depression: Further evidence for increased bacterial translocation or leaky gut

Maes, M., Kubera, M., Leunis, J.-C., & Berk, M. (2012) · Journal of Affective Disorders · doi:10.1016/j.jad.2012.02.023 · Cited by 446 · see citing works

Stress induces endotoxemia and low-grade inflammation by increasing barrier permeability

de Punder, K., & Pruimboom, L. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00223 · Cited by 321 · see citing works

Interplay between the gut-brain axis, obesity and cognitive function

Agustí, A., García-Pardo, M. P., López-Almela, I., Campillo, I., Maes, M., Romaní-Pérez, M., & Sanz, Y. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00155 · Cited by 294 · see citing works

Anti-inflammatory treatment for major depressive disorder: implications for patients with an elevated immune profile and non-responders to standard antidepressant therapy

Kopschina Feltes, P., Doorduin, J., Klein, H. C., Juárez-Orozco, L. E., Dierckx, R. A., Moriguchi-Jeckel, C. M., & de Vries, E. F. (2017) · Journal of Psychopharmacology · doi:10.1177/0269881117711708 · Cited by 279 · see citing works

Gut Microbiota, Bacterial Translocation, and Interactions with Diet: Pathophysiological Links between Major Depressive Disorder and Non-Communicable Medical Comorbidities

Slyepchenko, A., Maes, M., Jacka, F. N., Köhler, C. A., Barichello, T., McIntyre, R. S., Berk, M., Grande, I., Foster, J. A., Vieta, E., et al. (2017) · Psychotherapy and Psychosomatics · doi:10.1159/000448957 · Cited by 278 · see citing works

The Potential Role of Gut Microbiota in Alzheimer’s Disease: From Diagnosis to Treatment

Varesi, A., Pierella, E., Romeo, M., Piccini, G. B., Alfano, C., Bjørklund, G., Oppong, A., Ricevuti, G., Esposito, C., Chirumbolo, S., et al. (2022) · Nutrients · doi:10.3390/nu14030668 · Cited by 225 · see citing works

Changes in gut and plasma microbiome following exercise challenge in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)

Shukla, S. K., Cook, D., Meyer, J., Vernon, S. D., Le, T., Clevidence, D., Robertson, C. E., Schrodi, S. J., Yale, S., & Frank, D. N. (2015) · PLOS ONE · doi:10.1371/journal.pone.0145453 · Cited by 137 · see citing works

Diet, gut microbiota and cognition

Proctor, C., Thiennimitr, P., Chattipakorn, N., & Chattipakorn, S. C. (2017) · Metabolic Brain Disease · doi:10.1007/s11011-016-9917-8 · Cited by 144 · see citing works

Gut inflammation in chronic fatigue syndrome

Lakhan, S. E., & Kirchgessner, A. (2010) · Nutrition & Metabolism · doi:10.1186/1743-7075-7-79 · Cited by 143 · see citing works

Visceral Inflammation and Immune Activation Stress the Brain

Holzer, P., Farzi, A., Hassan, A. M., Zenz, G., Jačan, A., & Reichmann, F. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01613 · Cited by 84 · see citing works

Altered intestinal permeability in patients with primary fibromyalgia and in patients with complex regional pain syndrome

Goebel, A., Buhner, S., Schedel, R., Lochs, H., & Sprotte, G. (2008) · Rheumatology · doi:10.1093/rheumatology/ken140 · Cited by 76 · see citing works

Biocontrol of Morganella morganii subsp. morganii and Histamine Accumulation in Tuna Meat by Treatment with a Lytic Bacteriophage

Yamaki, S., Kawai, Y., & Yamazaki, K. (2018) · Food Science and Technology Research · doi:10.3136/fstr.24.329 · Cited by 9 · see citing works

TEM-72, a New Extended-Spectrum β-Lactamase Detected in Proteus mirabilis and Morganella morganii in Italy

Perilli, M., Segatore, B., Massis, M. R. D., et al. (2000) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.44.9.2537-2539.2000 · Cited by 34 · see citing works

Species interactions in mixed-community crystalline biofilms on urinary catheters

Macleod, S. M., & Stickler, D. J. (2007) · Journal of Medical Microbiology · doi:10.1099/jmm.0.47395-0 · Cited by 160 · see citing works

Description and plasmid characterization of qnrD determinants in Proteus mirabilis and Morganella morganii

Mazzariol, A., Kocsis, B., Koncan, R., et al. (2011) · Clinical Microbiology and Infection · doi:10.1111/j.1469-0691.2011.03728.x · Cited by 38 · see citing works

A Rare Opportunist, Morganella morganii , Decreases Severity of Polymicrobial Catheter-Associated Urinary Tract Infection

Learman, B. S., Brauer, A. L., Eaton, K. A., et al. (2019) · Infection and Immunity · doi:10.1128/iai.00691-19 · Cited by 33 · see citing works