Results 211 to 220 of about 800,833 (311)

A CASE OF ILEO-COLONIC FISTULA WHICH WAS ASSUMED TO BE CAUSED BY INTESTINAL TUBERCULOSIS

open access: bronze, 1996
Kazuo Kitabayashi   +5 more
openalex   +2 more sources

Hereditary angioedema as a cause of recurrent abdominal pain in a pediatric patient with Crohn's disease

open access: yesJPGN Reports, EarlyView.
Abstract Hereditary angioedema (HAE) is a rare genetic condition caused by deficient or dysfunctional C1 inhibitor protein (C1INH) resulting in episodic angioedema of the skin, upper airway, and gastrointestinal tract. HAE most often presents within the first two decades of life and may cause severe abdominal pain, nausea, diarrhea, and emesis, making ...
Stephanie L. Rager   +2 more
wiley   +1 more source

Problems of Nutritional and Metabolic Therapy of Patients with Intestinal Fistulas

open access: diamond
В. М. Луфт   +8 more
openalex   +1 more source

An incidental finding of mesenteric hematoma in a patient with a new diagnosis of inflammatory bowel disease

open access: yesJPGN Reports, EarlyView.
Abstract Mesenteric hematomas (MHs) are relatively rare and are characterized by localized bleeding in the mesenteric vascular tree presenting with abdominal pain, vomiting, abdominal distension, masses, and hypotension. We report a case of a MH which was incidentally found in a 10‐year‐old patient with a new diagnosis of ulcerative colitis (UC).
Breanna Brown   +2 more
wiley   +1 more source

Complex treatment of a patient with multiple external intestinal fistulas after pancreatoduodenal resection

open access: bronze, 1997
A. L. Lomonosov   +5 more
openalex   +2 more sources

Chronic atrial and intestinal dysrythmia syndrome: A late‐onset intestinal pseudo‐obstruction and cardiac dysfunction due to an SGO1 mutation

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Pediatric intestinal pseudo‐obstruction (PIPO) is a rare, heterogeneous, and severe gut motility disorder. In 2014, Chetaille et al. described chronic atrial and intestinal dysrhythmia (CAID) syndrome associated with a recessive SGO1 mutation (p.Lys23Glu) linking it to both intestinal pseudo‐obstruction and cardiac dysrhythmia. This
Linda Adouane   +4 more
wiley   +1 more source

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