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Congenital Short Bowel Syndrome: from clinical and genetic diagnosis to the molecular mechanisms involved in intestinal elongation

  • Published:2015-11 Issue:11 Volume:1852 Page:2352-2361
  • ISSN:0925-4439
  • Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
  • language:en
  • Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

van der Werf Christine S.,Halim Danny,Verheij Joke B.G.M.,Alves Maria M.,Hofstra Robert M.W.

Funder

Junior Scientific Masterclass (University of Groningen)

Ter Meulen Fund

van Walree Fund

Royal Netherlands Academy of Arts and Sciences

Dutch Digestive Foundation

J.K. de Cock Stichting

Stichting Simonsfonds

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference100 articles.

1. Short small intestine associated with malrotation: a newly described congenital cause of intestinal malabsorption;Hamilton;Gastroenterology,1969

2. CLMP is required for intestinal development, and loss-of-function mutations cause congenital short-bowel syndrome;Van Der Werf;Gastroenterology,2012

3. Congenital short bowel syndrome as the presenting symptom in male patients with FLNA mutations;van der Werf;Genet. Med.,2013

4. Congenital short-gut syndrome;Sabharwal;Pediatr. Radiol.,2004

5. Synovial lipomatosis (lipoma arborescens) affecting multiple joints in a patient with congenital short bowel syndrome;Siva;J. Rheumatol.,2002

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1. Congenital short bowel syndrome: Cases series in the same family and review of literature;International Journal of Surgery Case Reports;2024-10

2. Congenital abnormalities of the small intestine;Morson and Dawson's Gastrointestinal Pathology;2024-08-30

3. Ruptured giant omphalocele with congenital short small intestine: a case report;Frontiers in Nutrition;2024-07-18

4. The IgSF Cell Adhesion Protein CLMP and Congenital Short Bowel Syndrome (CSBS);International Journal of Molecular Sciences;2023-03-16

5. Physical organogenesis of the gut;Development;2022-08-15
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