Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M A Cournelle

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
La Revue Du Praticien|July 11, 2000
[Cognitive and socio-educational ramifications of epilepsy in the child]M O Livet, M A Cournelle, J Mancini
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Neuropsychological phenotypes of genetic diseases]M O Livet, M A Cournelle, A Moncla, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Information for the epileptic child]M O Livet, M A Cournelle, C Billard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Breast feeding: what role for the pediatrician]S Le Menestrel, N André, M A Cournelle, et al.
Pediatrie|January 1, 1993
[Study of risk factors for recurrence in severe life-threatening conditions in infants]Y Rimet, A Poujol, M A Cournelle, et al.
Archives Francaises De Pediatrie|February 1, 1993
[Dwarfism, arterial hypertension and hyperkalemic acidosis corrected with thiazides. A case of type II pseudohypoaldosteronism]A Poujol, Y Rimet, M A Cournelle, 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.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric aciduria: two further casesP Divry, C Jakobs, C Vianey-Saban, et al.
Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
La Revue Du Praticien|July 11, 2000
[Cognitive and socio-educational ramifications of epilepsy in the child]M O Livet, M A Cournelle, J Mancini
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Neuropsychological phenotypes of genetic diseases]M O Livet, M A Cournelle, A Moncla, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 25, 2000
[Information for the epileptic child]M O Livet, M A Cournelle, C Billard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 6, 1998
[Breast feeding: what role for the pediatrician]S Le Menestrel, N André, M A Cournelle, et al.
Pediatrie|January 1, 1993
[Study of risk factors for recurrence in severe life-threatening conditions in infants]Y Rimet, A Poujol, M A Cournelle, et al.
Archives Francaises De Pediatrie|February 1, 1993
[Dwarfism, arterial hypertension and hyperkalemic acidosis corrected with thiazides. A case of type II pseudohypoaldosteronism]A Poujol, Y Rimet, M A Cournelle, 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.
Journal of Inherited Metabolic Disease|January 1, 1993
L-2-hydroxyglutaric aciduria: two further casesP Divry, C Jakobs, C Vianey-Saban, et al.
Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.
Pageof 1