Results 101 to 110 of about 2,210 (159)

Protein-losing enteropathy in a patient on peritoneal dialysis

open access: yesNefrología (English Edition), 2017
Juan Egea-Valenzuela   +5 more
doaj   +1 more source

A case of systemic lupus erythematosus presenting with protein-losing enteropathy

open access: yesThe Turkish Journal of Gastroenterology, 2006
Nuran TÜRKÇAPAR   +7 more
doaj  

[Protein-losing enteropathies].

open access: yesPediatria polska, 1989
B, Lisowska-Myjak, L, Tomaszewski
openaire   +1 more source

[Protein-losing enteropathies].

open access: yesBoletin medico del Hospital Infantil de Mexico, 1981
openaire   +1 more source

Protein-Losing Enteropathy Associated with Henoch-Schönlein Purpura

open access: yesPediatric Reports, 2010
The gastrointestinal manifestations of Henoch-Schönlein purpura include abdominal pain, gastrointestinal bleeding, intussusception, and perforation. Protein-losing enteropathy is rarely associated with Henoch-Schönlein purpura.
Tatsuo Fuchigami, Yasuji Inamo
exaly   +4 more sources

Protein-losing enteropathy

open access: yesCurrent Opinion in Gastroenterology, 2020
Purpose of review The present review offers its readers a practical overview of protein-losing enteropathy, particularly with regard to diagnostic and therapeutic approaches. The aim is to support clinicians in their daily practice with a practical tool to deal with protein-losing enteropathy ...
Elli L., Topa M., Rimondi A.
openaire   +3 more sources
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Protein-Losing Enteropathy

Pediatric Clinics of North America, 1962
SummaryA man, aged 54 years, presented with œdema, ascites and hypoproteinæmia of 20 years' duration. Results of investigation of cardiac, renal and hepatic function were normal. There was no history suggesting a gastro‐intestinal disorder and investigation of bowel function was largely unproductive.
E. A. ESPINER, D. W. BEAVEN
  +5 more sources

Protein-losing enteropathies

Veterinary Clinics of North America: Small Animal Practice, 2003
GI protein loss can result from a heterogeneous group of diseases, including lymphangiectasia, IBD, neoplasia, ulceration, intussusception, and histoplasmosis. PLE should be suspected in any hypoalbuminemic patient with no evidence of exudative protein loss, proteinuria, or HI.
Polly B, Peterson, Michael D, Willard
openaire   +2 more sources

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