Search Results - "N'Guyen Morel, M A"

Superior parietal lobule dysfunction in a homogeneous group of dyslexic children with a visual attention span disorder by Peyrin, C., Démonet, J.F., N’Guyen-Morel, M.A., Le Bas, J.F., Valdois, S.

“…A visual attention (VA) span disorder has been reported in dyslexic children as potentially responsible for their poor reading outcome. The purpose of the…”
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Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathy by Rosas-Vargas, H, Bahi-Buisson, N, Philippe, C, Nectoux, J, Girard, B, N'Guyen Morel, M A, Gitiaux, C, Lazaro, L, Odent, S, Jonveaux, P, Chelly, J, Bienvenu, T

“…Mutations in the human X-linked cyclin-dependent kinase-like 5 (CDKL5) gene have been shown to cause infantile spasms as well as Rett syndrome-like phenotype…”
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Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases by Humbertclaude, V, Hamroun, D, Picot, M-C, Bezzou, K, Bérard, C, Boespflug-Tanguy, O, Bommelaer, C, Campana-Salort, E, Cances, C, Chabrol, B, Commare, M-C, Cuisset, J-M, de Lattre, C, Desnuelle, C, Echenne, B, Halbert, C, Jonquet, O, Labarre-Vila, A, N'guyen-Morel, M-A, Pages, M, Pepin, J-L, Petitjean, T, Pouget, J, Ollagnon-Roman, E, Richelme, C, Rivier, F, Sacconi, S, Tiffreau, V, Vuillerot, C, Béroud, C, Tuffery-Giraud, S, Claustres, M

“…The objective of this work was to study the natural history of dystrophinopathies and the genotype-phenotype correlations made possible by the development of…”
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Don’t forget methylmalonic acid quantification in symptomatic exclusively breast-fed infants by Van Noolen, L, Nguyen-Morel, M A, Faure, P, Corne, C

“…Vitamin B 12 deficiency can lead to serious haematological and neurological signs in infants. The reported clinical cases of vitamin B 12 deficiency were found…”
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Superior parietal lobule dysfunction in a homogeneous group of dyslexic children with a visual attention span disorder: Neural Representations in Visual Word Recognition by PEYRIN, C, DEMONET, J. F, N'GUYEN-MOREL, M. A, LE BAS, J. F, VALDOIS, S

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Don't forget methylmalonic acid quantification in symptomatic exclusively breast-fed infants : MATERNAL AND PEDIATRIC NUTRITION HIGHLIGHTS REVIEW by VAN NOOLEN, L, NGUYEN-MOREL, M. A, FAURE, P, CORNE, C

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Variabilité phénotypique et corrélations génotype-phénotype des dystrophinopathies: contribution des banques de données: Affections musculaires by HUMBERTCLAUDE, V, HAMROUN, D, COMMARE, M.-C, CUISSET, J.-M, DE LATTRE, C, DESNUELLE, C, ECHENNE, B, HALBERT, C, JONQUET, O, LABARRE-VILA, A, N'GUYEN-MOREL, M.-A, PAGES, M, PICOT, M.-C, PEPIN, J.-L, PETITJEAN, T, POUGET, J, OLLAGNON-ROMAN, E, RICHELME, C, RIVIER, F, SACCONI, S, TIFFREAU, V, VUILLEROT, C, BEROUD, C, BEZZOU, K, TUFFERY-GIRAUD, S, CLAUSTRES, M, BERARD, C, BOESPFLUG-TANGUY, O, BOMMELAER, C, CAMPANA-SALORT, E, CANCES, C, CHABROL, B

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Variabilité phénotypique et corrélations génotype-phénotype des dystrophinopathies : contribution des banques de données by Humbertclaude, V., Hamroun, D., Picot, M.-C., Bezzou, K., Bérard, C., Boespflug-Tanguy, O., Bommelaer, C., Campana-Salort, E., Cances, C., Chabrol, B., Commare, M.-C., Cuisset, J.-M., de Lattre, C., Desnuelle, C., Echenne, B., Halbert, C., Jonquet, O., Labarre-Vila, A., N’Guyen-Morel, M.-A., Pages, M., Pepin, J.-L., Petitjean, T., Pouget, J., Ollagnon-Roman, E., Richelme, C., Rivier, F., Sacconi, S., Tiffreau, V., Vuillerot, C., Béroud, C., Tuffery-Giraud, S., Claustres, M.

“…L’objectif de ce travail est d’étudier l’histoire naturelle des dystrophinopathies et les corrélations génotype-phénotype grâce au développement de la partie…”
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