Enrichment of Patients With Ehlers Danlos Syndrome in Idiopathic Gastroparesis—A Gene Set Enrichment Analysis-Reference-Cited by-同舟云学术

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Enrichment of Patients With Ehlers Danlos Syndrome in Idiopathic Gastroparesis—A Gene Set Enrichment Analysis

Published:2022-08-22 Issue:3 Volume:14 Page:e00521
ISSN:2155-384X
Container-title:Clinical and Translational Gastroenterology
language:en
Short-container-title:Clinical and Translational Gastroenterology

Author:

Smieszek Sandra P.,Carlin Jesse L.,Fisher Michaela A.,Madonick Darby S.,Kupersmith Caleigh Q.,Moszczynski Paula D.,Xiao Changfu,Polymeropoulos Christos M.,Birznieks Gunther,Polymeropoulos Mihael H.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Gastroenterology

Reference20 articles.

1. Homozygous Gly530Ser substitution in COL5A1 causes mild classical Ehlers-Danlos syndrome;Giunta;Am J Med Genet,2002

2. Nosology and inheritance pattern(s) of joint hypermobility syndrome and ehlers-Danlos syndrome, hypermobility type: A study of intrafamilial and interfamilial variability in 23 Italian pedigrees;Castori;Am J Med Genet Part A,2014

3. The genetic basis of the joint hypermobility syndromes;Malfait;Rheumatology,2006

4. Efficacy and safety of tradipitant in patients with diabetic and idiopathic gastroparesis in a randomized, placebo-controlled trial;Carlin;Gastroenterology,2021

5. Clinical guideline: Management of gastroparesis;Camilleri;Am J Gastroenterol,2013

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