Results 21 to 30 of about 9,951 (218)

A Case of Gastroduodenal Strongyloidiasis Causing Protein Losing Enteropathy

open access: yesJournal of Microbiology and Infectious Diseases, 2020
Strongylodiasis is an intestinal parasitic infection which can cause cataclysmic hyper infection syndrome in immunocompromised. Here we report an interesting and rare case of gastroduodenal strongyloidiasis presenting as protein losing enteropathy which ...
sandheep janardhanan   +5 more
doaj   +1 more source

Alterations in serum amino acid concentrations in dogs with protein-losing enteropathy [PDF]

open access: yes, 2018
BackgroundCertain amino acids are decreased in humans with inflammatory bowel disease (IBD) and supplementation with the same amino acids has shown beneficial effects in animal models of IBD.
Allenspach   +25 more
core   +4 more sources

A comprehensive pathological survey of duodenal biopsies from dogs with diet-responsive chronic enteropathy [PDF]

open access: yes, 2013
Background: The detailed pathological phenotype of diet-responsive chronic enteropathy (CE) and its modulation with dietary therapy remain poorly characterized. Hypothesis/Objectives: Key mucosal lesions of diet-responsive CE resolve with dietary therapy.
Alam   +71 more
core   +2 more sources

Urinary and faecal N-methylhistamine concentrations do not serve as markers for mast cell activation or clinical disease activity in dogs with chronic enteropathies [PDF]

open access: yes, 2014
This study sought to correlate faecal and urinary N-methylhistamine (NMH) concentrations with resting versus degranulated duodenal mast cell numbers in dogs with chronic enteropathies (CE), and investigate correlations between intestinal mast cell ...
Allenspach, K   +5 more
core   +4 more sources

Why is the skeleton still in the hospital closet? A look at the complex aetiology of protein-energy malnutrition and its implications for the nutrition care team [PDF]

open access: yes, 2018
Extract: The acknowledgement of protein-energy malnutrition (PEM) as one of “…the most serious nutritional problems of our time” was actually made by Dr Butterworth Jr in 1974 in his seminal article, “the skeleton in the hospital closet” (1).
Marshall, S.
core   +1 more source

Protein-losing enteropathy in systemic lupus erythematosus: case report [PDF]

open access: yes, 2012
Protein-losing enteropathy is rarely seen in patients with systemic lupus erythematosus. This clinical condition should be suspected in the presence of persistent hypoalbuminemia despite normal liver function, adequate protein intake, and no significant ...
Aguiar, Fernando Moreira Batista   +5 more
core   +3 more sources

Protein-Losing Enteropathy in Ulcerative Colitis

open access: yesCase Reports in Gastroenterology, 2012
Protein-losing enteropathy (PLE) is a debilitating potential complication of ulcerative colitis (UC). We report a case of PLE in a 26-year-old male patient with UC.
Ryan Ungaro   +3 more
doaj   +1 more source

Pathophysiology, Diagnosis, and Management of Canine Intestinal Lymphangiectasia: A Comparative Review

open access: yesAnimals, 2022
Intestinal lymphangiectasia was first described in the dog over 50 years ago. Despite this, canine IL remains poorly understood and challenging to manage.
Sara A. Jablonski
doaj   +1 more source

A Case of Protein Losing Enteropathy as Only Clinical manifestation of Systemic Lupus Erythematosus [PDF]

open access: yesKosin Medical Journal, 2017
Protein losing enteropathy (PLE) due to systemic lupus erythematosus (SLE) is relatively uncommon. PLE may be appeared sequentially after the diagnosis of SLE or concurrently with SLE.
Tae Hyun Kim   +5 more
doaj   +1 more source

Case report: Noonan syndrome with protein-losing enteropathy

open access: yesFrontiers in Genetics, 2023
Background: Noonan syndrome (NS) is characterized by typical facial features, short stature, congenital heart defects and other comorbidities. Lymphedema and chylous pleural effusions are also common in NS, but protein-losing enteropathy (PLE) is rarely ...
Yang Ou   +6 more
doaj   +1 more source

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