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santé - iate.europa.eu
santé - iate.europa.eu
santé - iate.europa.eu
santé - iate.europa.eu
A genetic study of hirschsprung disease.Hirschsprung disease, or congenital aganglionic megacolon, is commonly assumed to be a sex-modified multifactorial trait....
général - core.ac.uk - PDF: www.pubmedcentral.nih.gov
Neurogenic placodes provide migratory enteric sensory neural progenitors in response to endothelin signaling pathway... Abnormal development of ENS may cause the congenital aganglionic megacolon phenotype as Hirschsprung’s disease (HSCR)....
Null mutation of endothelin receptor type b gene in spotting lethal rats causes aganglionic megacolon and white coat color.Mutations in the gene encoding the endothelin receptor type B (EDNRB) produce congenital aganglionic megacolon and pigment abnormalities in mice and humans....
Functional aerophagia in children: a frequent, atypical disorder... Mechanical intestinal obstruction, chronic intestinal pseudo-obstruction, malabsorption and congenital aganglionic megacolon were ruled out....
 PDF: doaj.org
Congenital aganglionic megacolonTwenty-one pull-through procedures for congenital aganglionic megacolon (Hirschsprung's disease) have been performed at the Los Angeles Children's Hospital since the adoption of the etiological concept of a distal ...

Publications scientifiques

Long-term outcome of hirschsprung disease: impact on quality of life and social condition at adult ageBACKGROUND: Hirschsprung disease is a rare congenital disease typically requiring surgical treatment during childhood....
santé / activité agricole - core.ac.uk - PDF: okina.univ-angers.fr
Explaining change in quality of life of children and adolescents with anorectal malformations or hirschsprung disease...examine changes in quality of life, disease-specific functioning, and psychosocial competencies of children and adolescents (8-16 years of age) with anorectal malformations or Hirschsprung disease and to identify predictors of change in quality of life by testing an explanatory model in which background variables explained changes in quality of life...
santé - core.ac.uk - PDF: www.loc.gov
Down-regulation of circ-prkci inhibits cell migration and proliferation in hirschsprung disease by suppressing the expression of mir-1324 target plcb1... Hirschsprung disease (HSCR) is a well-known congenital gut motility disorder which roots in the aberrance of cranial-caudal neural crest cell migration....
santé - core.ac.uk - PDF: figshare.com
Waardenburg syndrome with isolated deficiency of myenteric ganglion cells at the sigmoid colon and rectum... When it is Hirschsprung disease (HD), the WS is diagnosed as type 4 WS....
santé - core.ac.uk - PDF: doaj.org
Gdnf haploinsufficiency causes hirschsprung-like intestinal obstruction and early-onset lethality in mice Hirschsprung disease (HSCR) is a common congenital disorder that results in intestinal obstruction and lethality, as a result of defective innervation of the gastrointestinal ...
santé - core.ac.uk -

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