Results 171 to 180 of about 55,733 (294)

Comparison of the bacterial flora of the duodenum in healthy cats and cats with signs of gastrointestinal tract disease [PDF]

open access: bronze, 2001
Karen L. Johnston   +6 more
openalex   +1 more source

Homozygosity for a variant in SLC10A2 and infancy onset severe fat‐soluble vitamin deficiency due to bile acid malabsorption

open access: yesJPGN Reports, EarlyView.
Abstract We present a case of a young female patient with persistent and severe fat‐soluble vitamin deficiency since infancy. Despite extensive investigations during childhood, the underlying cause remained elusive. The patient was generally asymptomatic while receiving continuous vitamin subsidy.
Christine Rungoe   +4 more
wiley   +1 more source

Elevated tissue transglutaminase immunoglobulin A: Celiac disease or polytypic plasmacytosis?

open access: yesJPGN Reports, EarlyView.
Abstract We report a case of an adolescent girl post cardiac transplant with hypergammaglobulinemia and presumed celiac disease (CD), who had a persistently elevated anti‐tissue transglutaminase immunoglobulin A despite a gluten free diet. Refractory CD and Crohn's disease were excluded.
Andrew Turunen   +4 more
wiley   +1 more source

The environmental impact of pediatric celiac disease diagnosis and follow‐up

open access: yesJPGN Reports, EarlyView.
ABSTRACT Objectives To evaluate carbon dioxide (CO2) footprint of celiac disease (CeD) diagnostic guidelines and follow‐up practices for children/adolescents. Methods Two‐hundred and thirty‐six patients diagnosed and followed up for CeD in Umbria region during 2020–2023 were included in this retrospective study.
Mario Brusco   +7 more
wiley   +1 more source

Efficacy of dual therapy vs. triple therapy for eradication of H. pylori in duodenal ulcer disease

open access: bronze, 1998
Bo Ohlin   +5 more
openalex   +1 more source

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

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