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M L Moutard

Showing results (21-30 of 52) with videos related to

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Anesthesiology|December 22, 1999
Changes in electroencephalogram and autonomic cardiovascular activity during induction of anesthesia with sevoflurane compared with halothane in childrenI Constant, M C Dubois, V Piat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 12, 2004
[Parent's information and prenatal diagnosis of cerebral malformation with an uncertain prognosis]M-L Moutard, I Fauriel, G Moutel, et al.
AJNR. American Journal of Neuroradiology|July 30, 2011
Biometry of the corpus callosum in children: MR imaging reference dataC Garel, I Cont, C Alberti, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 3, 2015
[A difficult transition from childhood to adult healthcare: the case of epilepsy]A-O Affdal, M-L Moutard, T Billette de Villemeur, et al.
Presse Medicale (Paris, France : 1983)|April 11, 1987
[Severe neonatal myasthenia with arthrogryposis]M L Moutard-Codou, M M Delleur, O Dulac, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 15, 2015
Abnormal shape of the cavum septi pellucidi: an indirect sign of partial agenesis of the corpus callosumO Shen, A B Gelot, M L Moutard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 16, 2006
[Fetal neurology: conditions of diagnostic uncertainty]M-L Moutard, A Gélot, D Rodriguez, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissuesF Degoul, D François, M Diry, et al.
Neuropediatrics|November 5, 2003
Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutationI Desguerre, F Pinton, R Nabbout, et al.
Fetal Diagnosis and Therapy|September 11, 2010
Prenatal diagnosis of 18q-syndrome: a case of fetal mosaicism with a normal karyotype in chorionic villiO Anselem, A Bazin, C Mechler, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Anesthesiology|December 22, 1999
Changes in electroencephalogram and autonomic cardiovascular activity during induction of anesthesia with sevoflurane compared with halothane in childrenI Constant, M C Dubois, V Piat, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 12, 2004
[Parent's information and prenatal diagnosis of cerebral malformation with an uncertain prognosis]M-L Moutard, I Fauriel, G Moutel, et al.
AJNR. American Journal of Neuroradiology|July 30, 2011
Biometry of the corpus callosum in children: MR imaging reference dataC Garel, I Cont, C Alberti, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 3, 2015
[A difficult transition from childhood to adult healthcare: the case of epilepsy]A-O Affdal, M-L Moutard, T Billette de Villemeur, et al.
Presse Medicale (Paris, France : 1983)|April 11, 1987
[Severe neonatal myasthenia with arthrogryposis]M L Moutard-Codou, M M Delleur, O Dulac, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 15, 2015
Abnormal shape of the cavum septi pellucidi: an indirect sign of partial agenesis of the corpus callosumO Shen, A B Gelot, M L Moutard, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 16, 2006
[Fetal neurology: conditions of diagnostic uncertainty]M-L Moutard, A Gélot, D Rodriguez, et al.
Journal of Inherited Metabolic Disease|March 1, 1997
A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissuesF Degoul, D François, M Diry, et al.
Neuropediatrics|November 5, 2003
Infantile spasms with basal ganglia MRI hypersignal may reveal mitochondrial disorder due to T8993G MT DNA mutationI Desguerre, F Pinton, R Nabbout, et al.
Fetal Diagnosis and Therapy|September 11, 2010
Prenatal diagnosis of 18q-syndrome: a case of fetal mosaicism with a normal karyotype in chorionic villiO Anselem, A Bazin, C Mechler, et al.
Pageof 6