Search Results - "Ginies, J L"

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    Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutations by Roussey, M., Le Bihannic, A., Scotet, V., Audrezet, M. P., Blayau, M., Dagorne, M., David, V., Deneuville, E., Giniès, J. L., Laurans, M., Moisan‐Petit, V., Rault, G., Vigneron, P., Férec, C.

    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 by Weil, B, Chaillou, E, Troussier, F, Pelatan, C, Chiffoleau, M, Darviot, E, Chevalier, M-C, Martin, L, Giniès, J-L

    “…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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    Chronic intestinal pseudoobstruction syndrome : Clinical analysis, outcome, and prognosis in 105 children by FAURE, C, GOULET, O, PAQUOT, I, HERMIER, M, DE NAPOLI, S, DABADIE, A, HUET, F, BAUDON, J.-J, LARCHET, M, ATEGBO, S, BRETON, A, TOUNIAN, P, GINIES, J.-L, ROQUELAURE, B, DESPRES, C, SCAILLON, M, MAURAGE, C

    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 by Malbrunot-Wagner, A C, Bridoux, L, Nousbaum, J B, Riou, C, Dirou, A, Ginies, J L, Maurage, C, Cagnard, B, Pelatan, C, Dabadie, A

    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 by Hubert, G, Giniès, J-L, Dabadie, A, Tourtelier, Y, Willot, S, Pariente, D, Lefrançois, T, Caldari, D

    “…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 by Allard, L, Giniès, J-L, Champion, G, Chevailler, A, Subra, J-F

    “…Antineutrophil cytoplasmic antibodies (ANCA) are usually considered as serological markers of vasculitis (microscopic polyangiitis, granulomatosis with…”
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    A Curable Cause of Chronic Idiopathic Intestinal Pseudo-Obstruction in Children: Idiopathic Myositis of the Small Intestine by Giniès, Jean-Louis, François, Henri, Joseph, Marie-Geneviève, Champion, Gérard, Coupris, Lionel, Limal, Jean-Marie

    “…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 by Malbrunot-Wagner, A-C, Bonnemains, C, Troussier, F, Darviot, E, Chiffoleau, M, Person, C, Urban, T, Giniès, J-L

    “…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 by Hubert, G., Giniès, J.-L., Dabadie, A., Tourtelier, Y., Willot, S., Pariente, D., Lefrançois, T., Caldari, D.

    “…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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    Auto-anticorps anticytoplasme des polynucléaires neutrophiles en pédiatrie : caractéristiques cliniques by Allard, L., Giniès, J.-L., Champion, G., Chevailler, A., Subra, J.-F.

    “…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 by Weil, B., Chaillou, E., Troussier, F., Pelatan, C., Chiffoleau, M., Darviot, E., Chevalier, M.-C., Martin, L., Giniès, J.-L.

    “…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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    Diarrhée néonatale par malabsorption du glucose et du galactose : à propos de 7 observations by Chedane-Girault, C., Dabadie, A., Maurage, C., Piloquet, H., Chailloux, E., Colin, E., Pelatan, C., Giniès, J.-L.

    “…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 by Beaumesnil, M., Chaillou, E., Wagner, A.-C., Rouquette, A., Audran, M., Giniès, J.-L.

    “…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 by Nicaise, D., Beaumesnil, M., Chaillou, E., Wagner, A.-C., Avarello, G., Audran, M., Giniès, J.-L.

    “…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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