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pro vyhledávání: '"J L Ginies"'
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Autor:
A C, Malbrunot-Wagner, L, Bridoux, J B, Nousbaum, C, Riou, A, Dirou, J L, Ginies, C, Maurage, B, Cagnard, C, Pelatan, A, Dabadie
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 10(5)
Esophageal varices (EV) are a complication of cystic fibrosis-associated liver disease. Esophagogastroduodenoscopy (EGD) is currently used to diagnose varices but is invasive for pediatric patients. The goal of this study was to explore the relations
Autor:
I, Sermet-Gaudelus, R, Nove-Josserand, G-A, Loeille, G, Dacremont, J-C, Souberbielle, J, Fritsch, M, Laurans, P, Moulin, B, Cortet, J-P, Salles, J-L, Ginies, M, Guillot, S, Perez-Martin, J-C, Ruiz, V, Montagne, M, Cohen-Solal, C, Cormier, M, Garabédian, E, Mallet, Carine, Wouters
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 15(3)
A high prevalence of low bone mineralization is documented in adult patients with cystic fibrosis (CF). Osteopenia is present in as much as 85% of adult patients and osteoporosis in 13 to 57% of them. In children, studies are discordant probably beca
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 8
Autor:
Marc Bellaiche, A. Morali, Jean Francois Duhamel, Thierry Lamireau, Chantal Maurage, J L Ginies, Jean Michel Vaillant, Sylvie Audrain, Jean Philippe Girardet, Jean Pierre Olives, Isabelle Pharaon, Jean Pierre Cezard, Jeanne Marie Lecomte, Jacques Sarles, Caroline Whately-Smith, Alain Poujol, M. Meyer
Publikováno v:
Gastroenterology. 120(4)
Background & Aims: Oral rehydration therapy is the only treatment recommended by the World Health Organization in acute diarrhea in children. Antisecretory drugs available could not be used because of their side effects, except for racecadotril, whic
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 6(7)
The aim of this study was to assess the bone mineral density of cystic fibrosis patients.We have retrospectively studied 45 patients with cystic fibrosis, 22 females and 23 males, aged between six and 27 years (mean 13 +/- 5.5 years). Nutritional sta
Autor:
C, Faure, O, Goulet, S, Ategbo, A, Breton, P, Tounian, J L, Ginies, B, Roquelaure, C, Despres, M, Scaillon, C, Maurage, I, Paquot, M, Hermier, S, De Napoli, A, Dabadie, F, Huet, J J, Baudon, M, Larchet
Publikováno v:
Digestive diseases and sciences. 44(5)
Our aim was to collect a large number of cases to characterize clinical presentation, outcome, and prognosis of chronic intestinal pseusoobstruction in children. We conducted a retrospective multicenter study that included children treated for chroni
Publikováno v:
Annales de dermatologie et de venereologie. 125(5)
Dorfman-Chanarin syndrome is an uncommon condition characterized by non-bullous congenital ichtyosiform erythrodermia and lipid vacuoles in circulating leukocytes.We report an unusual presentation in a child who had a dry congenital ichtyosiform eryt
Publikováno v:
Presse medicale (Paris, France : 1983). 26(33)
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 3(11)
Malformative uropathies diagnosed in utero are increasing in number. This work describes the decision strategy adopted in Angers concerning the neonatal handling of those abnormalities.One hundred children born between 1988 and 1990, with prenatally