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M O Livet

Showing results (41-50 of 53) with videos related to

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Developmental Medicine and Child Neurology|August 1, 1992
Epilepsy and focal gyral anomalies detected by MRI: electroclinico-morphological correlations and follow-upR Guerrini, C Dravet, C Raybaud, et al.
Developmental Medicine and Child Neurology|August 1, 1992
Neurological findings and seizure outcome in children with bilateral opercular macrogyric-like changes detected by MRIR Guerrini, C Dravet, C Raybaud, et al.
Archives Francaises De Pediatrie|April 1, 1978
[Evaluation of one year experience with cerebral tomodensitometry in pediatric neurology]N Pinsard, C Raybaud, J L Gastaut, et al.
Journal of Medical Genetics|July 29, 1999
Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counsellingA Moncla, P Malzac, M O Livet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 7, 2007
[Failure to thrive and psychomotor regression revealing vitamin B12 deficiency in 3 infants]C Mathey, J-N Di Marco, A Poujol, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 2, 2008
[EVAL MATER: Proposal for a paediatric evaluation of linguistic and psychomotor competences during the 1st medical check-up in nursery school]J Mancini, C Pech-Georgel, F Brun, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patientsA Moncla, P Malzac, M A Voelckel, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric aciduria: two further casesP Divry, C Jakobs, C Vianey-Saban, et al.
Blood|July 27, 2000
Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)C Valentin, S Pissard, J Martin, et al.
Annales De Pediatrie|September 1, 1978
[Craniostenoses]R Bernard, L Anquez, G Bosvieux, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Developmental Medicine and Child Neurology|August 1, 1992
Epilepsy and focal gyral anomalies detected by MRI: electroclinico-morphological correlations and follow-upR Guerrini, C Dravet, C Raybaud, et al.
Developmental Medicine and Child Neurology|August 1, 1992
Neurological findings and seizure outcome in children with bilateral opercular macrogyric-like changes detected by MRIR Guerrini, C Dravet, C Raybaud, et al.
Archives Francaises De Pediatrie|April 1, 1978
[Evaluation of one year experience with cerebral tomodensitometry in pediatric neurology]N Pinsard, C Raybaud, J L Gastaut, et al.
Journal of Medical Genetics|July 29, 1999
Angelman syndrome resulting from UBE3A mutations in 14 patients from eight families: clinical manifestations and genetic counsellingA Moncla, P Malzac, M O Livet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 7, 2007
[Failure to thrive and psychomotor regression revealing vitamin B12 deficiency in 3 infants]C Mathey, J-N Di Marco, A Poujol, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 2, 2008
[EVAL MATER: Proposal for a paediatric evaluation of linguistic and psychomotor competences during the 1st medical check-up in nursery school]J Mancini, C Pech-Georgel, F Brun, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patientsA Moncla, P Malzac, M A Voelckel, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric aciduria: two further casesP Divry, C Jakobs, C Vianey-Saban, et al.
Blood|July 27, 2000
Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)C Valentin, S Pissard, J Martin, et al.
Annales De Pediatrie|September 1, 1978
[Craniostenoses]R Bernard, L Anquez, G Bosvieux, et al.
Pageof 6