Search Results - "Odièvre, M."

Aggregatibacter actinomycetemcomitans infection in children: two case reports and a review of the literature by Karila-Cohen, J., Kerner, S., Blondiaux, E., Vimont, S., Odièvre, M. H., Fournier, B., Grimprel, E., Lorrot, M., Romain, A. S.

“…Aggregatibacter actinomycetemcomitans ( Aa ), a Gram-negative coccobacillus commonly associated with endocarditis, poses a rare diagnostic challenge in…”
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Drépanocytose chez l’enfant by Odièvre, M.-H., Quinet, B.

“…La drépanocytose, maladie génétique la plus fréquente en France, est non seulement une maladie de l’hémoglobine, mais aussi une maladie vasculaire associée à…”
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Pneumonia due to adenovirus type 7: a case report in a healthy infant by Odièvre, M-H, Danékova, N, Picard, C, Mesples, B, BenCheikha, Z, Avran, D, De Blic, J, Leruez-Ville, M, Parez, N

“…A 15-month-old boy treated with amoxicillin and clavulanic acid therapy for 8 days was admitted for persistent gastroenteritis and fever. He received…”
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Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases by Alagille, D, Estrada, A, Hadchouel, M, Gautier, M, Odièvre, M, Dommergues, J P

“…We have observed two types of paucity of interlobular bile ducts (PILBD) in children with chronic cholestasis: the syndromic type, which is more frequent (80…”
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Hypogonadisme hypergonadotrophique et galactosémie congénitale by Odièvre, M.-H., Labrune, P., Odièvre, M.

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Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene by Leclerc, Daniel, Odièvre, Marie-Hélène, Wu, Qing, Wilson, Aaron, Huizenga, Jack J, Rozen, Rima, Scherer, Stephen W, Gravel, Roy A

“…Methionine synthase reductase (EC 2.1.1.135) is a flavoprotein essential for maintenance of methionine synthase in an active state. We characterized the human…”
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Cytopathies mitochondriales secondaires chez l’enfant : concept récent, concept d’avenir ? by Odièvre, M.H, Lombès, A, Odièvre, M

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Partial effect of bromocriptine on lactose and galactose synthesis in a pregnant woman heterozygous for galactosaemia by ODIEVRE, M, BRIVET, M, RIVIERE, M-F, LABRUNE, P

“…Bromocriptine combined with galactose restriction in the matenal diet seems to be partially effective in decreasing endogenous lactose and galactose synthesis,…”
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Treatment of galactosemia: new strategies? by Odièvre, M

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Mutations in the phosphorylase kinase gene PHKA2 are responsible for X-linked liver glycogen storage disease by Hendrickx, J, Coucke, P, Dams, E, Lee, P, Odièvre, M, Corbeel, L, Fernandes, J F, Willems, P J

“…Phosphorylase kinase (PHK) is a key enzyme in the control of glycogen breakdown. Several types of PHK deficiency have been described of which X-linked liver…”
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Long-term outcome after surgery for biliary atresia. Study of 40 patients surviving for more than 10 years by Laurent, J, Gauthier, F, Bernard, O, Hadchouel, M, Odièvre, M, Valayer, J, Alagille, D

“…To define long-term prognosis of children who underwent surgery for biliary atresia, a retrospective study was undertaken in 122 children who underwent one of…”
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Le traitement de la galactosémie : de nouvelles stratégies ? by ODIEVRE, M

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Ondansetron for pruritus in child with chronic cholestasis by Trioche, P, Samuel, D, Odièvre, M, Labrune, P

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Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 cases by Labrune, P, Myara, A, Hadchouel, M, Ronchi, F, Bernard, O, Trivin, F, Chowdhury, N R, Chowdhury, J R, Munnich, A, Odièvre, M

“…Crigler-Najjar syndrome type I (CN-I) is an autosomal recessive condition characterized by severe unconjugated hyperbilirubinemia caused by the lack of…”
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Bilateral pulmonary embolism mimicking acute chest syndrome in an adolescent with sickle cell disease by Mornand, P, Chalard, F, Romain, A-S, Rohr, M, Paluel-Marmont, C, Niakaté, A, Quinet, B, Grimprel, E, Odièvre-Montanié, M-H

“…Pulmonary embolism is a life-threatening and potentially lethal disease. Its incidence in children with sickle cell disease is probably underestimated and…”
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Fratries d'enfants atteints de maladie chronique by ODIEVRE, M

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Drépanocytose chez l’enfant by Odièvre, M.H., Quinet, B.

“…La drépanocytose, maladie génétique la plus fréquente en France, est non seulement une maladie de l’hémoglobine, mais aussi une maladie vasculaire associée à…”
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Failure of cefotaxime treatment in two children with meningitis caused by highly penicillin-resistant Streptococcus pneumoniae by Guibert, M, Chahime, H, Petit, J, Odièvre, M, Labrune, P

“…Two infants, aged 8.5 and 11 months, were admitted for meningitis caused by Streptococcus pneumoniae. Failure of cefotaxime led to the identification of highly…”
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Sweet syndrome as the presenting manifestation of chronic granulomatous disease in an infant by Sedel, D, Huguet, P, Lebbe, C, Donadieu, J, Odièvre, M, Labrune, P

“…A 2.5-month-old infant had Sweet syndrome. Chronic granulomatous disease was subsequently diagnosed by the nitroblue tetrazolium reduction test. To date, this…”
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Accueil des parents d’enfants hospitalisés by ODIEVRE, M

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