Results 31 to 40 of about 66,104,498 (114)

Microbial infections in eight genomic subtypes of chronic fatigue syndrome/myalgic encephalomyelitis [PDF]

, 2010
BACKGROUND: The authors have previously reported genomic subtypes of chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) based on expression of 88 human genes.
Gough, J, Kerr, JR, Honeybourne, David, Richards, SC, Ayres, JG, Mattey, DL, Enlander, D, Zhang, L, Ayres, Jonathan, Richards, Selwyn C M, Christmas, D, Main, J, Honeybourne, D, Nutt, DJ   +13 more
core   +1 more source

Single‐operator single‐balloon enteroscopy is safe and effective: A 6‐year retrospective study

Journal of Digestive Diseases, Volume 25, Issue 6, Page 353-360, June 2024.
In total, 922 patents with 1422 single‐operator single‐balloon enteroscopy (SBE) procedures were enrolled in the study. Based on the analyses of diagnostic yield, total enteroscopy rate, duration, insertion depth, and complications, and stratification analysis of the above parameters, the single‐operator SBE technique was found to be effective, safe ...
Guan Jun Kou, Chao Liu, Yan Bo Yu, Yan Qing Li, Xiu Li Zuo   +4 more
wiley   +1 more source

Response to combination therapy with interferon alfa-2a and ribavirin in chronic hepatitis C according to a TNF-alpha promoter polymorphism [PDF]

, 2003
Background. Tumor necrosis factor-alpha (TNF-alpha) is involved in the pathogenesis of chronic active hepatitis C. Polymorphisms in the promoter region of the TNF-alpha gene can alter the TNF-alpha expression and modify the host immune response.
Konig, A., Folwaczny, Christian, Schmidt, F., Simperl, C., Schaefer, M., Torok, P., Glas, J., Schiemann, Uwe, Martin, K.   +8 more
core   +1 more source

Intestinal Permeability in Dogs with Chronic Enteropathy [PDF]

, 2023
Dogs with chronic clinical signs of gastrointestinal disease such as diarrhea, vomiting, weight loss, and/or loss of appetite are often diagnosed with chronic enteropathy after infectious, parasitic, neoplasia, and extra-intestinal diseases have been ...
Ishii Miyagawa, Patricia Eri
core   +1 more source

Monogenic SLCO2A1 gene mutation presenting as early onset inflammatory bowel disease-A report of rare case with review of literature

Indian Journal of Pathology and Microbiology
Chronic enteropathy associated with the SLCO2A1 gene (CEAS) is a rare, autosomal recessive disorder characterized by multiple chronic ulcerative and structuring lesions in the small intestine, primarily affecting the ileum.
Mukund Namdev Sable, M. Shameema Farween, Susama Patra, Saswati Kar, Subash Chandra Samal   +4 more
doaj   +1 more source

Olmesartan-Associated Enteropathy: An Unexpected Cause of Chronic Diarrhoea [PDF]

, 2019
Olmesartan-associated enteropathy is a rare cause of severe enteropathy that should be considered in the differential diagnosis of patients with unexplained chronic diarrhoea.
Mónica Martins Teixeira, Maria Costa, António Novais, Martins, Ana Sofia, Eugénia Maria Cancela, Ana Sofia Martins, Sara Macedo, Novais, António, Macedo, Sara, Teixeira, Mónica Martins, Tânia Batista, Costa, Maria, Cancela, Eugénia Maria, Batista, Tânia   +13 more
core   +1 more source

Biallelic SLCO2A1 variants in two siblings with primary hypertrophic osteoarthropathy and possible chronic enteropathy

Frontiers in Endocrinology
Background and aimsPathogenic variants in the SLCO2A1 gene are responsible for two rare monogenic disorders: primary hypertrophic osteoarthropathy (PHO) and chronic enteropathy (CEAS).
Tao Wang, Qian Zhang, Tingting Shi, Xin Chen, Li Wang, Xiuming Liu, Yihui Wang, Kaikai Shen, Fei Zhao, Litao Qin   +9 more
doaj   +1 more source

Association of the CCR5 gene with juvenile idiopathic arthritis [PDF]

, 2010
The CC chemokine receptor 5 (CCR5) has been shown to be important in the recruitment of T-helper cells to the synovium, where they accumulate, drive the inflammatory process and the consequent synovitis and joint destruction.
Martin, P., BSPAR Study Group, Barton, A., UKRAG Consortium, Worthington, J., Gardner-Medwin, J. [CAPS and BSPAR Study Groups], Thomson, W., W Thomson, Flynn, E., A Hinks, E Flynn, J Packham, Packham, J., Hinks, A., S Eyre, J Worthington, Eyre, S.; id_orcid, Eyre, S., Barton, A.; id_orcid, P Martin, Childhood Arthritis Prospective Study (CAPS), Martin, P.; id_orcid, A Barton   +22 more
core   +1 more source

A frequent variant in the human bile salt export pump gene ABCB11 is associated with hepatitis C virus infection, but not liver stiffness in a German population [PDF]

, 2012
Background: The human ATP-binding cassette, subfamily B, member 11 (ABCB11) gene encodes the bile salt export pump, which is exclusively expressed at the canalicular membrane of hepatocytes.
Müllenbach, Roman, Marcin Krawczyk, Weber, Susanne N., Grünhage, Frank, Sarrazin, Christoph, Zimmer, Vincent, Frank Grünhage, Krawczyk, Marcin, Lammert, Frank, Christoph Sarrazin, Roman Müllenbach, Susanne N Weber, Vincent Zimmer, Frank Lammert   +13 more
core   +2 more sources

Long-chain PUFA supplementation in rural African infants: a randomized controlled trial of effects on gut integrity, growth, and cognitive development. [PDF]

, 2013
BACKGROUND: Intestinal damage and malabsorption caused by chronic environmental enteropathy are associated with growth faltering seen in infants in less-developed countries.
Drammeh, Saikou, Stephen Young, Andrew M Prentice, van der Merwe, Liandré F, Young, Stephen, Fulford, Anthony J, Halliday, Katherine E, Prentice, Andrew M, Saikou Drammeh, Sophie E Moore, Anthony J Fulford, Moore, Sophie E, Liandré F van der Merwe, Katherine E Halliday   +13 more
core   +1 more source