This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.
Lewandowska-Pietruszka Z, Figlerowicz M, Mazur-Melewska K. The History of the Intestinal Microbiota and the Gut-Brain Axis. Pathogens. 2022;11(12):1540. doi:10.3390/pathogens11121540Open DOISearch in Google Scholar
Nanthakumaran S, Sridharan S, Somagutta MR, et al. The Gut-Brain Axis and Its Role in Depression. Cureus. 2020;12(9). doi:10.7759/cureus.10280Open DOISearch in Google Scholar
La microbiota intestinal y surelación con las enfermedadesmentales a través del eje microbiotaintestino-cerebro. Accessed July 11, 2023. http://riberdis.cedid.es/handle/11181/5361Search in Google Scholar
Liu Y, Sanderson D, Mian MF, McVey Neufeld KA, Forsythe P. Loss of vagal integrity disrupts immune components of the microbiota-gut-brain axis and inhibits the effect of Lactobacillus rhamnosus on behavior and the corticosterone stress response. Neuropharmacology. 2021;195:108682. doi:10.1016/j.neuropharm.2021.108682Open DOISearch in Google Scholar
Gorecki AM, Dunlop SA, Rodger J, Anderton RS. The gut-brain axis and gut inflammation in Parkinson's disease: stopping neurodegeneration at the toll gate. Expert Opinion on Therapeutic Targets. 2020;24(7):601-604. doi:10.1080/14728222.2020.1763956Open DOISearch in Google Scholar
Mayer EA, Nance K, Chen S. The Gut–Brain Axis. Annual Review of Medicine. 2022;73(1):439-453. doi:10.1146/annurev-med-042320-014032Open DOISearch in Google Scholar
Xie Y, Zhou G, Wang C, Xu X, Li C. Specific Microbiota Dynamically Regulate the Bidirectional Gut–Brain Axis Communications in Mice Fed Meat Protein Diets. J Agric Food Chem. 2019;67(3):1003-1017. doi:10.1021/acs.jafc.8b05654Open DOISearch in Google Scholar
Jandhyala SM, Talukdar R, Subramanyam C, Vuyyuru H, Sasikala M, Reddy DN. Role of the normal gut microbiota. World J Gastroenterol. 2015;21(29):8787-8803. doi:10.3748/wjg.v21.i29.8787Open DOISearch in Google Scholar
Kennedy EA, King KY, Baldridge MT. Mouse Microbiota Models: Comparing Germ-Free Mice and Antibiotics Treatment as Tools for Modifying Gut Bacteria. Frontiers in Physiology. 2018;9. Accessed July 11, 2023. https://www.frontiersin.org/articles/10.3389/fphys.2018.01534Search in Google Scholar
Bajaj JS, Barbara G, DuPont HL, Mearin F, Gasbarrini A, Tack J. New concepts on intestinal microbiota and the role of the non-absorbable antibiotics with special reference to rifaximin in digestive diseases. Dig Liver Dis. 2018 Aug;50(8):741-749. doi: 10.1016/j.dld.2018.04.020.Open DOISearch in Google Scholar
Khoruts A. Targeting the microbiome: from probiotics to fecal microbiota transplantation. Genome Medicine. 2018;10(1):80. doi:10.1186/s13073-018-0592-8Open DOISearch in Google Scholar
Thursby E, Juge N. Introduction to the human gut microbiota. Biochemical Journal. 2017;474(11):1823-1836. doi:10.1042/BCJ20160510Open DOISearch in Google Scholar
Yoo JY, Groer M, Dutra SVO, Sarkar A, McSkimming DI. Gut Microbiota and Immune System Interactions. Microorganisms. 2020;8(10):1587. doi:10.3390/microorganisms8101587Open DOISearch in Google Scholar
Pickard JM, Zeng MY, Caruso R, Núñez G. Gut microbiota: Role in pathogen colonization, immune responses, and inflammatory disease. Immunological Reviews. 2017;279(1):70-89. doi:10.1111/imr.12567Open DOISearch in Google Scholar
Hong SW, O E, Lee JY, et al. Food antigens drive spontaneous IgE elevation in the absence of commensal microbiota. Science Advances. 2019;5(5):eaaw1507. doi:10.1126/sciadv.aaw1507Open DOISearch in Google Scholar
Gao C, Major A, Rendon D, et al. Histamine H2 Receptor-Mediated Suppression of Intestinal Inflammation by Probiotic Lactobacillus reuteri. mBio. 2015;6(6):10. 1128/mbio. 01358-15. doi:10.1128/mbio.01358-15Open DOISearch in Google Scholar
Caetano-Silva ME, Rund L, Hutchinson NT, Woods JA, Steelman AJ, Johnson RW. Inhibition of inflammatory microglia by dietary fiber and short-chain fatty acids. Sci Rep. 2023;13(1):2819. doi:10.1038/s41598-022-27086-xOpen DOISearch in Google Scholar
Dicks LMT. Gut Bacteria and Neurotransmitters. Microorganisms. 2022;10(9):1838. doi:10.3390/microorganisms10091838Open DOISearch in Google Scholar
Silva YP, Bernardi A, Frozza RL. The Role of Short-Chain Fatty Acids From Gut Microbiota in Gut-Brain Communication. Front Endocrinol (Lausanne). 2020;11:25. doi:10.3389/fendo.2020.00025Open DOISearch in Google Scholar
Farzi A, Fröhlich EE, Holzer P. Gut Microbiota and the Neuroendocrine System. Neurotherapeutics. 2018;15(1):5-22. doi:10.1007/s13311-017-0600-5Open DOISearch in Google Scholar
Portincasa P, Bonfrate L, Vacca M, et al. Gut Microbiota and Short Chain Fatty Acids: Implications in Glucose Homeostasis. International Journal of Molecular Sciences. 2022;23(3):1105. doi:10.3390/ijms23031105Open DOISearch in Google Scholar
Zhao L, Zhang F, Ding X, et al. Gut bacteria selectively promoted by dietary fibers alleviate type 2 diabetes. Science. 2018;359(6380):1151-1156. doi:10.1126/science.aao5774Open DOISearch in Google Scholar
De la Cuesta-Zuluaga J, Mueller NT, Álvarez-Quintero R, et al. Higher Fecal Short-Chain Fatty Acid Levels Are Associated with Gut Microbiome Dysbiosis, Obesity, Hypertension and Cardiometabolic Disease Risk Factors. Nutrients. 2019;11(1):51. doi:10.3390/nu11010051Open DOISearch in Google Scholar
Tsigalou C, Paraschaki A, Karvelas A, et al. Gut microbiome and Mediterranean diet in the context of obesity. Current knowledge, perspectives and potential therapeutic targets. Metabolism Open. 2021;9:100081. doi:10.1016/j.metop.2021.100081Open DOISearch in Google Scholar
Arhire LI, Padureanu SS, Gherasim A, Nita O, Oprescu AC, Gavril RS, Mihalache L. Is there a need for one-month medical follow-up after laparoscopic sleeve gastrectomy? Obes Surg. 2018; 28 (1): S107.Search in Google Scholar
Han H, Yi B, Zhong R, et al. From gut microbiota to host appetite: gut microbiota-derived metabolites as key regulators. Microbiome. 2021;9:162. doi:10.1186/s40168-021-01093-yOpen DOISearch in Google Scholar
Mihalache L, Gherasim A, Ni ă O, Ungureanu MC, Pădureanu SS, Gavril RS, Arhire LI. Effects of ghrelin in energy balance and body weight homeostasis. Hormones. 2016; 15(2): 186-196.Search in Google Scholar
Gavril OI, Arhire LI, Gavril RS, et al. Correlations between PNPLA3 Gene Polymorphisms and NAFLD in Type 2 Diabetic Patients. Medicina. 2021; 57(11): 1249.Search in Google Scholar
Gupta A, Osadchiy V, Mayer EA. Brain-gut-microbiome interactions in obesity and food addiction. Nat Rev Gastroenterol Hepatol. 2020 Nov;17(11):655-672. doi: 10.1038/s41575-020-0341-5Open DOISearch in Google Scholar
Ma J, Piao X, Mahfuz S, Long S, Wang J. The interaction among gut microbes, the intestinal barrier and short chain fatty acids. Animal Nutrition. 2022;9:159-174. doi:10.1016/j.aninu.2021.09.012Open DOISearch in Google Scholar
Willemsen LEM, Koetsier MA, van Deventer SJH, van Tol EAF. Short chain fatty acids stimulate epithelial mucin 2 expression through differential effects on prostaglandin E1 and E2 production by intestinal myofibroblasts. Gut. 2003;52(10):1442-1447. Accessed July 11, 2023. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1773837/Search in Google Scholar
Camilleri M. The Leaky Gut: Mechanisms, Measurement and Clinical Implications in Humans. Gut. 2019;68(8):1516-1526. doi:10.1136/gutjnl-2019-318427Open DOISearch in Google Scholar
Stewart AS, Pratt-Phillips S, Gonzalez LM. Alterations in Intestinal Permeability: The Role of the “Leaky Gut” in Health and Disease. Journal of Equine Veterinary Science. 2017;52:10-22. doi:10.1016/j.jevs.2017.02.009Open DOISearch in Google Scholar
Camilleri M, Vella A. What to do about the leaky gut. Gut. 2022;71(2):424-435. doi:10.1136/gutjnl-2021-325428Open DOISearch in Google Scholar
Camilleri M. What is the leaky gut? Clinical considerations in humans. Current Opinion in Clinical Nutrition & Metabolic Care. 2021;24(5):473. doi:10.1097/MCO.0000000000000778Open DOISearch in Google Scholar
Leaky brain in neurological and psychiatric disorders: Drivers and consequences - Gerwyn Morris, Brisa S Fernandes, Basant K Puri, Adam J Walker, Andre F Carvalho, Michael Berk, 2018. Accessed July 12, 2023. https://journals.sagepub.com/doi/full/10.1177/0004867418796955Search in Google Scholar
Wu H, Wang J, Teng T, et al. Biomarkers of intestinal permeability and blood-brain barrier permeability in adolescents with major depressive disorder. Journal of Affective Disorders. 2023;323:659-666. doi:10.1016/j.jad.2022.11.058Open DOISearch in Google Scholar
Luczynski P, McVey Neufeld KA, Oriach CS, Clarke G, Dinan TG, Cryan JF. Growing up in a bubble: using germ-free animals to assess the influence of the gut microbiota on brain and behavior. International Journal of Neuropsychopharmacology. 2016 Aug 1;19(8):pyw020.Search in Google Scholar
Bercik P, Collins SM, Verdu EF. Microbes and the gut-brain axis. Neurogastroenterology& Motility. 2012;24(5):405-413. doi:10.1111/j.1365-2982.2012. 01906.xOpen DOISearch in Google Scholar
Kim HS. Do an Altered Gut Microbiota and an Associated Leaky Gut Affect COVID-19 Severity? mBio. 2021;12(1):10.1128/mbio.03022-20. doi:10.1128/mbio.03022-20Open DOISearch in Google Scholar
Zhang Y, Geng X, Tan Y, et al. New understanding of the damage of SARS-CoV-2 infection outside the respiratory system. Biomed Pharmacother. 2020;127:110195. doi:10.1016/j.biopha.2020.110195Open DOISearch in Google Scholar
Karim A, Muhammad T, Ustrana S, Qaisar R. Intestinal permeability marker zonulin as a predictor of sarcopenia in chronic obstructive pulmonary disease. Respiratory Medicine. 2021;189:106662. doi:10.1016/j.rmed.2021.106662Open DOISearch in Google Scholar
Li N, Dai Z, Wang Z, et al. Gut microbiota dysbiosis contributes to the development of chronic obstructive pulmonary disease. Respir Res. 2021;22:274. doi:10.1186/s12931-021-01872-zOpen DOISearch in Google Scholar
Paray BA, Albeshr MF, Jan AT, Rather IA. Leaky Gut and Autoimmunity: An Intricate Balance in Individuals Health and the Diseased State. Int J Mol Sci. 2020;21(24):9770. doi:10.3390/ijms21249770Open DOISearch in Google Scholar
Berer K, Gerdes LA, Cekanaviciute E, et al. Gut microbiota from multiple sclerosis patients enables spontaneous autoimmune encephalomyelitis in mice. Proceedings of the National Academy of Sciences. 2017;114(40):10719-10724. doi:10.1073/pnas.1711233114Open DOISearch in Google Scholar
Damci T, Nuhoglu I, Devranoglu G, Osar Z, Demir M, Ilkova H. Increased intestinal permeability as a cause of fluctuating postprandial blood glucose levels in Type 1 diabetic patients. European journal of clinical investigation. 2003 May;33(5):397-401.Search in Google Scholar
Watts T, Berti I, Sapone A, et al. Role of the intestinal tight junction modulator zonulin in the pathogenesis of type I diabetes in BB diabetic-prone rats. Proc Natl Acad Sci U S A. 2005;102(8):2916-2921. doi:10.1073/pnas.0500178102Open DOISearch in Google Scholar
Yeoh N, Burton JP, Suppiah P, Reid G, Stebbings S. The Role of the Microbiome in Rheumatic Diseases. CurrRheumatol Rep. 2013;15(3):314. doi:10.1007/s11926 -012-0314-yOpen DOISearch in Google Scholar
Audo R, Sanchez P, Rivière B, et al. Rheumatoid arthritis is associated with increased gut permeability and bacterial translocation that are reversed by inflammation control. Rheumatology. 2023;62(3):1264-1271. doi:10.1093/rheumatology/keac454Open DOISearch in Google Scholar
Zhong D, Wu C, Zeng X, Wang Q. The role of gut microbiota in the pathogenesis of rheumatic diseases. Clin Rheumatol. 2018;37(1):25-34. doi:10.1007/s10067-017-3821-4Open DOISearch in Google Scholar
ZununiVahed S, Barzegari A, Zuluaga M, Letourneur D, Pavon-Djavid G. Myocardial infarction and gut microbiota: An incidental connection. Pharmacological Research. 2018;129:308-317. doi:10.1016/j.phrs.2017.11.008Open DOISearch in Google Scholar
Novakovic M, Rout A, Kingsley T, et al. Role of gut microbiota in cardiovascular diseases. World J Cardiol. 2020;12(4):110-122. doi:10.4330/wjc.v12.i4.110Open DOISearch in Google Scholar
Gavril RS, Mastaleru A, Mitu O, et al. Cardiovascular Risk Assesment in Nonalcoholic Fatty Liver Disease. Filodiritto Editore Proceedings. 2018: 38-41.Search in Google Scholar
Liu Y, Dai M. Trimethylamine N-Oxide Generated by the Gut Microbiota Is Associated with Vascular Inflammation: New Insights into Atherosclerosis. Mediators Inflamm. 2020;2020:4634172. doi:10.1155/2020/4634172Open DOISearch in Google Scholar
Zhu Y, Li Q, Jiang H. Gut microbiota in atherosclerosis: focus on trimethylamine N-oxide. APMIS. 2020;128(5):353-366. doi:10.1111/apm.13038Open DOISearch in Google Scholar
Tacconi E, Palma G, De Biase D, et al. Microbiota Effect on Trimethylamine N-Oxide Production: From Cancer to Fitness—A Practical Preventing Recommendation and Therapies. Nutrients. 2023;15(3):563. doi:10.3390/nu15030563Open DOISearch in Google Scholar
He Z, Chen ZY. The origin of trimethylamine-N-oxide (TMAO) and its role in development of atherosclerosis. Journal of Food Bioactives. 2018;2:28-36. doi:10.31665/JFB.2018.2138Open DOISearch in Google Scholar
Lau WL, Vaziri ND. The Leaky Gut and Altered Microbiome in Chronic Kidney Disease. Journal of Renal Nutrition. 2017;27(6):458-461. doi:10.1053/j.jrn.2017.02.010Open DOISearch in Google Scholar
Lau WL, Savoj J, Nakata MB, Vaziri ND. Altered microbiome in chronic kidney disease: systemic effects of gut-derived uremic toxins. Clin Sci (Lond). 2018;132(5):509-522. doi:10.1042/CS20171107Open DOISearch in Google Scholar
Rydzewska-Rosołowska A, Sroka N, Kakareko K, Rosołowski M, Zbroch E, Hryszko T. The Links between Microbiome and Uremic Toxins in Acute Kidney Injury: Beyond Gut Feeling—A Systematic Review. Toxins. 2020;12(12):788. doi:10.3390/toxins12120788Open DOISearch in Google Scholar
Stengel A, Gourcerol G, Taché Y. Neurogastroenterology–Focus on the Gut-Brain Axis. Frontiers in Psychiatry. 2021 Mar 4;12:653910.Search in Google Scholar
Durgan DJ, Lee J, McCullough LD, Bryan RM Jr. Examining the Role of the Microbiota-Gut-Brain Axis in Stroke. Stroke. 2019 Aug;50(8):2270-2277. doi: 10.1161/STROKEAHA.119.025140. Epub 2019 Jul 5. PMID: 31272315; PMCID: PMC6646086.Open DOISearch in Google Scholar
Sinagra E, Pellegatta G, Guarnotta V, Maida M, Rossi F, Conoscenti G, Pallio S, Alloro R, Raimondo D, Pace F, Anderloni A. Microbiota gut–brain axis in ischemic stroke: a narrative review with a focus about the relationship with inflammatory bowel disease. Life. 2021 Jul 19;11(7):715.Search in Google Scholar
Benakis C, Liesz A. The gut-brain axis in ischemic stroke: its relevance in pathology and as a therapeutic target. Neurol Res Pract. 2022;4(1):57. doi:10.1186/s42466-022-00222-8Open DOISearch in Google Scholar
Zhang M na, Shi Y dan, Jiang H yin. The risk of dementia in patients with inflammatory bowel disease: a systematic review and meta-analysis. Int J Colorectal Dis. 2022;37(4):769-775. doi:10.1007/s00384-022-04131-9Open DOISearch in Google Scholar
A. Kohler C, Maes M, Slyepchenko A, et al. The Gut-Brain Axis, Including the Microbiome, Leaky Gut and Bacterial Translocation: Mechanisms and Pathophysiological Role in Alzheimer's Disease. Current Pharmaceutical Design. 2016;22(40):6152-6166.Search in Google Scholar
Cells | Free Full-Text | Gut Microbiota, Its Role in Induction of Alzheimer's Disease Pathology, and Possible Therapeutic Interventions: Special Focus on Anthocyanins. Accessed July 12, 2023. https://www.mdpi.com/2073-4409/9/4/853Search in Google Scholar
Yang D, Zhao D, Ali Shah SZ, et al. The Role of the Gut Microbiota in the Pathogenesis of Parkinson's Disease. Frontiers in Neurology. 2019;10. Accessed July 12, 2023. https://www.frontiersin.org/articles/10.3389/fneur.2019.01155Search in Google Scholar
Dong S, Sun M, He C, Cheng H. Brain-gut-microbiota axis in Parkinson's disease: A historical review and future perspective. Brain Research Bulletin. 2022;183:84-93. doi:10.1016/j.brainresbull.2022.02.015Open DOISearch in Google Scholar
Caiaffo V, Oliveira BD, de Sá FB, Evêncio Neto J. Anti-inflammatory, antiapoptotic, and antioxidant activity of fluoxetine. Pharmacology research & perspectives. 2016 Jun;4(3):e00231.Search in Google Scholar
Gałecki P, Mossakowska-Wójcik J, Talarowska M. The anti-inflammatory mechanism of antidepressants – SSRIs, SNRIs. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 2018;80:291-294. doi:10.1016/j.pnpbp.2017.03.016Open DOISearch in Google Scholar
Dinan TG, Stanton C, Cryan JF. Psychobiotics: A Novel Class of Psychotropic. Biological Psychiatry. 2013;74(10):720-726. doi:10.1016/j.biopsych.2013.05.001Open DOISearch in Google Scholar
Cheng LH, Liu YW, Wu CC, Wang S, Tsai YC. Psychobiotics in mental health, neurodegenerative and neurodevelopmental disorders. Journal of Food and Drug Analysis. 2019;27(3):632-648. doi:10.1016/j.jfda.2019.01.002Open DOISearch in Google Scholar
Evrensel A, Ünsalver BÖ, Ceylan ME. Psychobiotics. In: Kim YK, ed. Frontiers in Psychiatry: Artificial Intelligence, Precision Medicine, and Other Paradigm Shifts. Advances in Experimental Medicine and Biology. Springer; 2019:565-581. doi:10.1007/978-981-32-9721-0_28Open DOISearch in Google Scholar
Bauer KC, Huus KE, Finlay BB. Microbes and the mind: emerging hallmarks of the gut microbiota–brain axis. Cellular Microbiology. 2016;18(5):632-644. doi:10.1111/cmi.12585Open DOISearch in Google Scholar
Vuong HE, Hsiao EY. Emerging Roles for the Gut Microbiome in Autism Spectrum Disorder. Biological Psychiatry. 2017;81(5):411-423. doi:10.1016/j.biopsych.2016.08.024Open DOISearch in Google Scholar
The microbiome and gut homeostasis | Science. Accessed July 12, 2023. https://www.science.org/doi/full/10.1126/science.abp9960Search in Google Scholar
QIN, Da, et al. Contribution of Lactobacilli on Intestinal Mucosal Barrier and Diseases: Perspectives and Challenges of Lactobacillus casei. Life, 2022, 12.11: 1910.Search in Google Scholar
RANUH, Reza, et al. Effect of the probiotic Lactobacillus plantarum IS-10506 on BDNF and 5HT stimulation: Role of intestinal microbiota on the gut-brain axis. Iranian Journal of Microbiology, 2019, 11.2: 145.Search in Google Scholar
Martoni CJ, Srivastava S, Leyer GJ. Lactobacillus acidophilus DDS-1 and Bifidobacterium lactis UABla-12 improve abdominal pain severity and symptomology in irritable bowel syndrome: randomized controlled trial. Nutrients. 2020 Jan 30;12(2):363.Search in Google Scholar
Tette FM, Kwofie SK, Wilson MD. Therapeutic anti-depressant potential of microbial GABA produced by Lactobacillus rhamnosus strains for GABAergic signaling restoration and inhibition of addiction-induced HPA axis hyperactivity. Current Issues in Molecular Biology. 2022 Mar 22;44(4):1434-51.Search in Google Scholar
Sushma G, Vaidya B, Sharma S, et al. Bifidobacterium breve Bif11 supplementation improves depression-related neurobehavioural and neuroinflammatory changes in the mouse. Neuropharmacology. 2023;229:109480. doi:10.1016/j.neuropharm.2023.109480Open DOISearch in Google Scholar
Fattorusso A, Di Genova L, Dell'Isola GB, Mencaroni E, Esposito S. Autism spectrum disorders and the gut microbiota. Nutrients. 2019 Feb 28;11(3):521.Search in Google Scholar
Abdel-Wahab BA, F. Abd El-Kareem H, Alzamami A, A. Fahmy C, H. Elesawy B, Mostafa Mahmoud M, Ghareeb A, El Askary A, H. Abo Nahas H, GM Attallah N, Altwaijry N. Novel exopolysaccharide from marine Bacillus subtilis with broad potential biological activities: Insights into antioxidant, anti-Inflammatory, cytotoxicity, and anti-Alzheimer activity. Metabolites. 2022 Jul 31;12(8):715.Search in Google Scholar
Siesto G, Pietrafesa R, Infantino V, Thanh C, Pappalardo I, Romano P, Capece A. In vitro study of probiotic, antioxidant and anti-inflammatory activities among indigenous Saccharomyces cerevisiae strains. Foods. 2022 May 5;11(9):1342.Search in Google Scholar
Yaghoubfar R, Behrouzi A, Ashrafian F, Shahryari A, Moradi HR, Choopani S, Hadifar S, Vaziri F, Nojoumi SA, Fateh A, Khatami S. Modulation of serotonin signaling/metabolism by Akkermansiamuciniphila and its extracellular vesicles through the gut-brain axis in mice. Scientific reports. 2020 Dec 17;10(1):22119.Search in Google Scholar
Liu M, Zhang X, Hao Y, Ding J, Shen J, Xue Z, Qi W, Li Z, Song Y, Zhang T, Wang N. Protective effects of a novel probiotic strain, Lactococcus lactis ML2018, in colitis: in vivo and in vitro evidence. Food & function. 2019;10(2):1132-45.Search in Google Scholar
Hiergeist A, Gessner J, Gessner A. Current limitations for the assessment of the role of the gut microbiome for attention deficit hyperactivity disorder (ADHD). Frontiers in Psychiatry. 2020 Jun 26;11:623.Search in Google Scholar
SUN, Jing, et al. Effect of Clostridium butyricum against microglia-mediated neuroinflammation in Alzheimer's disease via regulating gut microbiota and metabolites butyrate. Molecular nutrition & food research, 2020, 64.2: 1900636.Search in Google Scholar
Chen L, Reynolds C, David R, Peace Brewer A. Development of an Index Score for Intestinal Inflammation-Associated Dysbiosis Using Real-World Stool Test Results. Dig Dis Sci. 2020;65(4):1111-1124. doi:10.1007/s10620-019-05828-8.Open DOISearch in Google Scholar
