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pro vyhledávání: '"Fibrosing colonopathy"'
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Akademický článek
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Autor:
Alexandra Wald, Jan Tuennemann, Thomas Karlas, Robert Henker, Albrecht Hoffmeister, Hubert Wirtz, Annett Oltmanns, Sabine Opitz, Joachim Mössner, Boris Jansen-Winkeln
Publikováno v:
Zeitschrift für Gastroenterologie. 57:312-316
The relevance of gastrointestinal manifestations of cystic fibrosis (CF) is increasing due to an improved life expectancy. We report on 2 adult patients with prior lung transplantation who presented with a severe inflammatory disorder of the ileoceca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86f8a8e35936c0186386d882c9e011d6
https://doi.org/10.1055/a-0829-7050
https://doi.org/10.1055/a-0829-7050
Publikováno v:
Journal of Pediatric Surgery.
Background Restorative proctocolectomy (RPC) is performed using a variety of staged procedures for several diseases. Our aim was to assess whether the severity of complications, classified according to Clavien–Dindo, was related to the diagnosis or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1abba81825b28fbc4b9382820749d0e
https://doi.org/10.1016/j.jpedsurg.2020.08.023
https://doi.org/10.1016/j.jpedsurg.2020.08.023
Publikováno v:
Clinics in Colon and Rectal Surgery. 31:121-126
Cystic fibrosis is one of the most common inheritable traits in Caucasians. Meconium ileus and its potential complications are the most likely reasons that these patients will need surgical care. Surgical intervention is usually needed in the neonata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6998bcf974b892e9548422cc9ba0b95b
https://doi.org/10.1055/s-0037-1609027
https://doi.org/10.1055/s-0037-1609027
Publikováno v:
European Journal of Pediatrics. 175:881-894
Cystic fibrosis is a life shortening hereditary disease, primarily leading to progressive pulmonary infection and exocrine pancreatic dysfunction. Several gastrointestinal complications other than malabsorption can arise during the disease course and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08d8d7c8267e99d298392b5fba71a0e1
https://doi.org/10.1007/s00431-016-2719-5
https://doi.org/10.1007/s00431-016-2719-5
Publikováno v:
European Journal of Medical Research, Vol 16, Iss 9, p 411 (2011)
Abstract Objective Fibrosing colonopathy (FC) is a rare entity associated with cystic fibrosis (CF). Until now, patients with stricturing FC have usually been treated surgically. In this instance, we aimed at avoiding surgery by applying a new conser
Externí odkaz:
https://doaj.org/article/af2589374f6b489491f93bbd5c69d6d0
Autor:
Eric Heffernan, Dermot E. Malone, Elaine Ni Mhurchu, Lisa P. Lavelle, Robert G. Gibney, Sinead H. McEvoy, Colm J. McMahon
Publikováno v:
RadioGraphics. 35:680-695
Cystic fibrosis (CF) is the most common lethal autosomal recessive disease in the white population. Mutation of the CF transmembrane conductance regulator gene on chromosome 7 results in production of abnormally viscous mucus and secretions in the lu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::194306f82cd79833483ec74885a0e4d2
https://doi.org/10.1148/rg.2015140110
https://doi.org/10.1148/rg.2015140110
Autor:
Samuel Bitton, Michael J. Pettei
Publikováno v:
Pediatrics In Review. 37:85-87
1. Samuel Bitton, MD* 2. Michael J Pettei, MD, PhD* 1. *Hofstra North Shore-LIJ School of Medicine/Steven and Alexandra Cohen Children's Medical Center of NY, Lake Success, NY. 1. 1. Taylor CJ, 2. Chen K, 3. Horvath K, 4. et al ESPGHAN and NASPGHAN R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54f8be8864ab2dc8bb3f214bd2695ddd
https://doi.org/10.1542/pir.2015-0084
https://doi.org/10.1542/pir.2015-0084