Zobrazeno 1 - 10
of 75
pro vyhledávání: '"M. O. Livet"'
Publikováno v:
EMC - Pediatría. 44:1-10
Publikováno v:
EMC - Pédiatrie - Maladies infectieuses. 3:1-10
Publikováno v:
Developmental Medicine & Child Neurology. 44:391-398
Publikováno v:
Neuropsychiatrie de l'Enfance et de l'Adolescence. 54:159-164
Resume Le syndrome de Williams est un syndrome neurodeveloppemental d'origine genetique. Ce syndrome se caracterise par une grande heterogeneite des fonctions cognitives, certaines etant preservees comme le langage, la musique, et la reconnaissance d
Publikováno v:
Archives de Pédiatrie. 9:709-725
The identification of an etiology in children with mental deficiency is a major challenge in routine pediatrics. As the result of a workshop leaded by the Societe francaise de neurologie pediatrique (SFNP), we propose a three steps diagnostic procedu
Autor:
Andrea Ballabio, Francesca Moro, M. O. Livet, Renzo Guerrini, Daniela T. Pilz, Pierangelo Veggiotti, Emilio Fernandez-Alvarez, Alessandra Renieri, Antonella Fogli, Elena Rossi, Maddalena Cioni, Romeo Carrozzo
Publikováno v:
Annals of Neurology. 45:154-161
We report on the genotype–phenotype correlation in 7 patients with classical lissencephaly carrying a heterozygous subtle mutation in the LIS1 gene. Six patients showed a mutation predicted to encode for a truncated protein, and one mutation altere
Autor:
J, Mancini, C, Pech-Georgel, F, Brun, F, George, M O, Livet, R, Camps, A, Massoulier, E, Suzineau, V, Guagliardo, P, Verger
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 15(4)
To prevent learning disorders, the authors propose a standardized approach of linguistic competences and psychomotor development in young children.Children were evaluated during the systematic examination that was carried out in nursery school betwee
Autor:
C, Mathey, J-N, Di Marco, A, Poujol, M-A, Cournelle, V, Brevaut, M-O, Livet, B, Chabrol, G, Michel
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 14(5)
The newborn's vitamin B12 storage exclusively comes from placenta transfer, later from animal food. We relate 3 observations of infants (3-11-13 months) with failure to thrive, anorexia, vomiting and for the two olders refusal of weaning, associated
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 9(7)
The identification of an etiology in children with mental deficiency is a major challenge in routine pediatrics. As the result of a workshop leaded by the Société française de neurologie pédiatrique (SFNP), we propose a three steps diagnostic pro
Publikováno v:
Developmental medicine and child neurology. 44(6)
The Battery for Rapid Evaluation of Cognitive Functions (Batterie Rapide d'Evaluation des Fonctions Cognitives: BREV) is a quick test to screen children with higher-functioning disorders and to define the patterns of their disorders. After standardiz