Microvillus inclusion disease-Reference-Cited by-同舟云学术

Microvillus inclusion disease

Published:1991 Issue:3 Volume:100 Page:811-817
ISSN:0016-5085
Container-title:Gastroenterology
language:en
Short-container-title:Gastroenterology

Author:

Rhoads J. Marc,Vogler Robert C.,Lacey Stuart R.,Reddick Robert L.,Keku Emmanuel O.,Azizkhan Richard G.,Berschneider Helen M.

Publisher

Elsevier BV

Subject

Gastroenterology,Hepatology

Reference29 articles.

1. Familial enteropathy: a syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villus atrophy;Davidson;Gastroenterology,1978

2. Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation;Cutz;N Engl J Med,1989

3. Congenital microvillous atrophy: specific diagnostic features;Phillips;Arch Dis Child,1985

4. Intravenous epidermal growth factor/urogastrone increases small intestinal proliferation in congenital microvillous atrophy;Walker-Smith;Lancet,1985

5. Urogastrone/epidermal growth factor in treatment of congenital microvillous atrophy;Drumm;Lancet,1988

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1. Weight loss and metabolic acidosis in a neonate: Answers;Pediatric Nephrology;2023-01-04

2. Loss of Serum Glucocorticoid-Inducible Kinase 1 SGK1 Worsens Malabsorption and Diarrhea in Microvillus Inclusion Disease (MVID);Journal of Clinical Medicine;2022-07-19

3. Altered MYO5B Function Underlies Microvillus Inclusion Disease: Opportunities for Intervention at a Cellular Level;Cellular and Molecular Gastroenterology and Hepatology;2022

4. Pharmacological and Parenteral Nutrition-Based Interventions in Microvillus Inclusion Disease;Journal of Clinical Medicine;2020-12-23

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