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Showing results (101-110 of 156) with videos related to

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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.
Acta Neuropathologica|January 1, 1995
Developmental aspects of type II lissencephaly. Comparative study of dysplastic lesions in fetal and post-natal brainsA Gelot, T Billette de Villemeur, C Bordarier, et al.
The New England Journal of Medicine|October 10, 1985
Detection of measles virus RNA in lymphocytes from peripheral-blood and brain perivascular infiltrates of patients with subacute sclerosing panencephalitisJ G Fournier, M Tardieu, P Lebon, et al.
Brain : a Journal of Neurology|March 2, 1999
DYT1 mutation in French families with idiopathic torsion dystoniaA S Lebre, A Durr, P Jedynak, et al.
Archives Francaises De Pediatrie|March 1, 1993
[Herpes encephalitis in newborn infants. Retrospective study of 12 cases]J Bigotte, J C Mselati, M C Routon, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1994
Reappraisal of Rasmussen's syndrome with special emphasis on treatment with high doses of steroidsD Chinchilla, O Dulac, O Robain, et al.
Acta Neuropathologica|July 10, 2004
Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic studyR De Armas, P Sindou, A Gelot, et al.
Radiology|October 1, 1987
Hemimegalencephaly: MR imaging in five childrenG L Kalifa, C Chiron, N Sellier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 7, 1999
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin]J M Pinard, C Marsac, E Barkaoui, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutationF Degoul, M Diry, D Rodriguez, et al.
Pageof 16

Showing results (101-110 of 156) with videos related to

Sort By:
Pageof 16
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.
Acta Neuropathologica|January 1, 1995
Developmental aspects of type II lissencephaly. Comparative study of dysplastic lesions in fetal and post-natal brainsA Gelot, T Billette de Villemeur, C Bordarier, et al.
The New England Journal of Medicine|October 10, 1985
Detection of measles virus RNA in lymphocytes from peripheral-blood and brain perivascular infiltrates of patients with subacute sclerosing panencephalitisJ G Fournier, M Tardieu, P Lebon, et al.
Brain : a Journal of Neurology|March 2, 1999
DYT1 mutation in French families with idiopathic torsion dystoniaA S Lebre, A Durr, P Jedynak, et al.
Archives Francaises De Pediatrie|March 1, 1993
[Herpes encephalitis in newborn infants. Retrospective study of 12 cases]J Bigotte, J C Mselati, M C Routon, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1994
Reappraisal of Rasmussen's syndrome with special emphasis on treatment with high doses of steroidsD Chinchilla, O Dulac, O Robain, et al.
Acta Neuropathologica|July 10, 2004
Demyelinating peripheral neuropathy associated with hemophagocytic lymphohistiocytosis. An immuno-electron microscopic studyR De Armas, P Sindou, A Gelot, et al.
Radiology|October 1, 1987
Hemimegalencephaly: MR imaging in five childrenG L Kalifa, C Chiron, N Sellier, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 7, 1999
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin]J M Pinard, C Marsac, E Barkaoui, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Clinical, biochemical, and molecular analysis of a maternally inherited case of Leigh syndrome (MILS) associated with the mtDNA T8993G point mutationF Degoul, M Diry, D Rodriguez, et al.
Pageof 16