Results 31 to 40 of about 59,884 (365)
Intestinal pseudo-obstruction caused by Giardia lamblia infection. [PDF]
Pessarelli T+3 more
europepmc +3 more sources
A Case of Chronic Intestinal Pseudo-Obstruction [PDF]
Scleroderma is a systemic disease characterized by the deposition of excessive collagen and other matrix elements in the skin as well as in multiple internal organs.
Matt Baichi
openalex +4 more sources
Prucalopride for chronic intestinal pseudo‐obstruction [PDF]
Pantelis Oustamanolakis, Jan Tack
openalex +4 more sources
Endoscopic Management of Benign Colonic Obstruction and Pseudo-Obstruction [PDF]
There are a variety of causes of intestinal obstruction, with the most common cause being malignant diseases; however, volvulus, inflammatory bowel disease or diverticulitis, radiation injury, ischemia, and pseudo-obstruction can also cause colonic ...
Su Jin Jeong, Jongha Park
doaj +1 more source
Familial Pernicious Chronic Intestinal Pseudo-obstruction with a Mitochondrial DNA A3243G Mutation
Junichiro Suzuki+5 more
exaly +2 more sources
Chronic intestinal pseudo-obstruction (CIPO) is caused by metabolic and endocrine factors, but it can also be caused by the cancer's paraneoplastic effect.
Deniz Esin Tekcan Şanlı+5 more
doaj +1 more source
Intestinal pseudo-obstruction: A rare presentation of congenital hypothyroidism. [PDF]
Peña-Vélez R+4 more
europepmc +2 more sources
The 5HT4R agonist velusetrag efficacy on neuropathic chronic intestinal pseudo-obstruction in PrP-SCA7-92Q transgenic mice. [PDF]
Liu Y+11 more
europepmc +3 more sources
Gastrointestinal motility disorders involve alterations to the structure and/or function of the enteric nervous system (ENS) but the causal mechanisms remain unresolved in most cases. Homeostasis and disease in the ENS are processes that are regulated by
Mohammad M. Ahmadzai+6 more
semanticscholar +1 more source
Mitochondrial neurogastrointestinal encephalomyopathy: approaches to diagnosis and treatment [PDF]
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is an ultra-rare disease caused by mutations in TYMP, the gene encoding for the enzyme thymidine phosphorylase.
Bax, BE
core +1 more source