Search Results - "Ginies, J L"
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Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutations
Published in Journal of inherited metabolic disease (01-08-2007)“…Summary Newborn screening (NBS) of cystic fibrosis (CF) was implemented throughout the whole of France in 2002, but it had been established earlier in three…”
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Aquagenic palmoplantar keratoderma in children with cystic fibrosis
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-12-2013)“…Aquagenic palmoplantar keratoderma (APK) is a cutaneous phenomenon marked by the formation of edematous, translucent papules and plaques on the palms after…”
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Knowledge of adolescents with inflammatory bowel disease: Results of a multicenter cross-sectional survey
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-05-2015)“…To assess knowledge acquired by adolescents about their inflammatory bowel disease (IBD). An anonymous questionnaire was given during consultation to…”
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Chronic intestinal pseudoobstruction syndrome : Clinical analysis, outcome, and prognosis in 105 children
Published in Digestive diseases and sciences (01-05-1999)“…Our aim was to collect a large number of cases to characterize clinical presentation, outcome, and prognosis of chronic intestinal pseusoobstruction in…”
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Transient elastography and portal hypertension in pediatric patients with cystic fibrosis Transient elastography and cystic fibrosis
Published in Journal of cystic fibrosis (01-09-2011)“…Esophageal varices (EV) are a complication of cystic fibrosis-associated liver disease. Esophagogastroduodenoscopy (EGD) is currently used to diagnose varices…”
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Congenital portosystemic shunts: experience of the western region of France over 5 years
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-11-2014)“…Congenital portosystemic shunts (CPS) are rare vascular malformations that lead to liver metabolic modifications. The aim of this study was to describe the…”
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Antineutrophil cytoplasmic autoantibodies in children: clinical features
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-03-2013)“…Antineutrophil cytoplasmic antibodies (ANCA) are usually considered as serological markers of vasculitis (microscopic polyangiitis, granulomatosis with…”
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Body composition analysis in patients with cystic fibrosis. Comparison of 3 methods: dual energy x-ray absorptiometry, bioelectrical impedance analysis, and skinfold measurements
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-04-2011)“…Nutritional status must be closely monitored in cystic fibrosis (CF) patients. This study compared three methods of measuring body composition in CF patients…”
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A Curable Cause of Chronic Idiopathic Intestinal Pseudo-Obstruction in Children: Idiopathic Myositis of the Small Intestine
Published in Journal of pediatric gastroenterology and nutrition (01-11-1996)“…SUMMARYWe report an intestinal pseudo-obstruction syndrome occurring in a 6-month-old infant girl suffering from acquired major and persistent abdominal…”
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Transition from pediatric to adult care: experience of a cystic fibrosis care center
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-03-2009)“…Even though patients with cystic fibrosis (CF) are continuously improving their life expectancy, guidelines for transition to adult services have not been…”
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Shunts porto-systémiques congénitaux : expérience du Grand-Ouest sur cinq ans
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-11-2014)“…Les shunts porto-systémiques congénitaux (SPSC) sont des malformations vasculaires rares, entraînant des modifications du métabolisme hépatique. Le but de ce…”
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Efficacy and tolerability of racecadotril in acute diarrhea in children
Published in Gastroenterology (New York, N.Y. 1943) (01-03-2001)“…Background & Aims: Oral rehydration therapy is the only treatment recommended by the World Health Organization in acute diarrhea in children. Antisecretory…”
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Auto-anticorps anticytoplasme des polynucléaires neutrophiles en pédiatrie : caractéristiques cliniques
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-03-2013)“…Les anticorps anticytoplasme des polynucléaires neutrophiles (antineutrophil cytoplasmic autoantibodies [ANCA]) sont des marqueurs de vascularites…”
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Kératodermie palmoplantaire aquagénique chez l’enfant mucoviscidosique
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-12-2013)“…La kératodermie palmoplantaire aquagénique (KPA) est une dermatose des paumes et des plantes dont les signes (œdème, majoration des plis et papules…”
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Hepatopulmonary Syndrome in a Child with Cystic Fibrosis
Published in Journal of pediatric gastroenterology and nutrition (01-11-1996)Get full text
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Hypomagnesemia after liver transplantation in children
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-08-2013)Get full text
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Diarrhée néonatale par malabsorption du glucose et du galactose : à propos de 7 observations
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-12-2012)“…Les intolérances aux sucres sont une cause classique de diarrhée à début néonatal. Nous en rapportons 7 observations d’étiologie particulière : la…”
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Composition corporelle des patients mucoviscidosiques – comparaison de 3 techniques de mesure : anthropométrie, absorptiométrie biphotonique et impédancemétrie
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-04-2011)“…La surveillance de l’état nutritionnel est essentielle dans la mucoviscidose. Le but de ce travail était de comparer chez ces patients 3 méthodes de mesure de…”
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Anorexie mentale de l’adolescent : conséquences sur la minéralisation osseuse
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (2012)“…L’anorexie mentale est responsable d’anomalies de la minéralisation osseuse connues et décrites chez l’adulte, mais beaucoup moins documentées chez…”
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