Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Olivier De Dreuzy"'
Autor:
Slimane Allali, Jean-Baptiste Muller, Raja Brauner, Diana Lourenço, Radia Boudjenah, Vasiliki Karageorgou, Christine Trivin, Henri Lottmann, Stephen Lortat-Jacob, Claire Nihoul-Fékété, Olivier De Dreuzy, Ken McElreavey, Anu Bashamboo
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e24117 (2011)
BACKGROUND: Mutations of the NR5A1 gene encoding steroidogenic factor-1 have been reported in association with a wide spectrum of 46,XY DSD (Disorder of Sex Development) phenotypes including severe forms of hypospadias. METHODOLOGY/PRINCIPAL FINDINGS
Externí odkaz:
https://doaj.org/article/d05b61189b364974bec123afba8f5069
Autor:
Frédéric Gauthier, Philippe Montupet, Blandine Roblot-Maigret, Mario Mendoza-Sagaon, Olivier de Dreuzy
Publikováno v:
Pediatric Endosurgery & Innovative Techniques. 5:305-308
Background: The laparoscopic approach for antireflux surgery is becoming the gold standard for children with gastroesophageal reflux disease (GERD) when surgical treatment is indicated. Preferences for a partial or a full fundoplication still relate
Autor:
Sophie Branchereau, Jacques Valayer, Dominique Debray, Christophe Chardot, Yumi Okawa, Frédéric Gauthier, Olivier de Dreuzy, Denis Devictor, Didier Jacolot
Publikováno v:
The Tohoku Journal of Experimental Medicine. 181:129-138
According to French rules for cadaver organ sharing, children with biliary atresia (BA) complicated with acute necrosis (ALN) can be registered on the waiting list for liver transplantation (LT) in a special intermediate grade urgent code. Over a 7 y
Publikováno v:
Pediatric Surgery International. 11:8-13
An abdominal or pelvic tumor in very seldom detected in a prenatal ultrasound examination. The most commonly detected tumors are, in order of decreasing frequency, sacrococcygeal teratomas, neuroblastomas and kidney tumors. According to the present s
Autor:
Ken McElreavey, Claire Nihoul-Fékété, Radia Boudjenah, Stephen Lortat-Jacob, Christine Trivin, Olivier De Dreuzy, Anu Bashamboo, Raja Brauner, Diana Lourenco, Henri Lottmann, Jean-Baptiste Muller, Vasiliki Karageorgou, Slimane Allali
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e24117 (2011)
PLoS ONE
PLoS ONE; Vol 6
PLoS ONE
PLoS ONE; Vol 6
Background Mutations of the NR5A1 gene encoding steroidogenic factor-1 have been reported in association with a wide spectrum of 46,XY DSD (Disorder of Sex Development) phenotypes including severe forms of hypospadias. Methodology/Principal Findings
Autor:
Philippe Montupet, Mario Mendoza-Sagaon, Olivier De Dreuzy, Blandine Roblot-Maigret, Frederic Gauthier
Publikováno v:
Pediatric Endosurgery & Innovative Techniques; Sep2001, Vol. 5 Issue 3, p305-308, 4p