Results 21 to 30 of about 144,432 (333)
Collagenous Enterocolitis: A Rare Condition with Simultaneous Involvement of the Upper and Lower Gastrointestinal Tract [PDF]
Journal of Clinical and Diagnostic Research, 2023 Collagenous colitis is a form of microscopic colitis, while Collagenous Sprue (CS) is a malabsorptive disorder that mimics celiac disease. Both conditions show increased Intraepithelial Lymphocytes (IELs) and basement membrane thickening due to collagen ...
Ankita Asthana +4 more
doaj +1 more source
Lithium toxicity following Roux-en-Y gastric bypass: Mini review and illustrative case [PDF]
Mental Health Clinician, 2022 Lithium is among the mainstays of treatment for bipolar disorder. Bariatric surgery can considerably change the oral bioavailability of drugs, particularly lithium.
Shahana Ayub, MD +5 more
doaj +1 more source
Specific features of impaired intestinal digestion, absorption, and microbiocenosis in patients with cholelithiasis [PDF]
Терапевтический архив, 2017 Aim. To perform a comprehensive study of intestinal digestion, absorption, and microbiocenosis in various stages of cholelithiasis (CL). Subjects and methods.
Ya M Vakhrushev, А Р Lukashevich
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Frontiers in Endocrinology, 2021 Approximately, 5% of the population is affected by hypothyroidism, mainly women and persons aged more than 60 years. After the diagnosis of hypothyroidism the usual therapy is tablet levothyroxine (L-T4), with a monitoring of the thyroid-stimulating ...
Alessandro Antonelli +9 more
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Secondary exocrine pancreatic insufficiency. Features of the choice of the enzyme
Медицинский совет, 2021 Exocrine pancreatic insufficiency is quite common in clinical practice of doctors of many specialties. Decrease in intraduodenal lipase levels below 5–10% of normal leads to pancreatic steatorrhea, weight loss and a potential decrease in quality of life.
I. G. Pakhomova
doaj +1 more source
Hereditary folate malabsorption
Definitions, 2020 Hereditary folate malabsorption (HFM) is an inherited disorder of folate transport characterized by a systemic and central nervous system (CNS) folate deficiency manifesting as megaloblastic anemia, failure to thrive, diarrhea and/or oral mucositis ...
semanticscholar +1 more source
Enteroendocrine Dysfunction in Two Saudi Sisters
Case Reports in Gastroenterology, 2021 Proprotein convertase (PC) deficiency is a rare autosomal recessive disorder caused by mutations in proprotein convertase subtilisin/kexin type 1 (PCSK1).
Amna Basheer M. Ahmed +1 more
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Frontiers in Physiology, 2022 Using metadata from previously published research, this investigation sought to explore: (1) whole-body total carbohydrate and fat oxidation rates of endurance (e.g., half and full marathon) and ultra-endurance runners during an incremental exercise test
Christopher E. Rauch +3 more
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Hepatology, EarlyView., 2022 Abstract Background and Aims Peroxisome proliferator‐activated receptor α (PPARα) regulates fatty acid transport and catabolism in liver. However, the role of intestinal PPARα in lipid homeostasis is largely unknown. Here, intestinal PPARα was examined for its modulation of obesity and NASH. Approach and Results Intestinal PPARα was activated and fatty
Tingting Yan +22 more
wiley +1 more source
CSF Obstruction and Malabsorption in Congenital Hydrocephalus
Pediatric Neurology Briefs, 2006 The relative contribution of CSF malabsorption and obstruction in three different etiological groups of neonatal high-pressure hydrocephalus (HC) was assessed in a study at University of Bonn, Germany, and University of Groningen, The Netherlands.
J Gordon Millichap
doaj +1 more source