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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 12, 2000
[Epilepsy presenting as life-threatening events in infants]L Heissessen, A Dusser, V Nouirygat, et al.The Journal of Pediatrics|November 5, 1997
Segregation of the G8993 mutant mitochondrial DNA through generations and embryonic tissues in a family at risk of Leigh syndromeT Ferlin, P Landrieu, C Rambaud, et al.Archives Francaises De Pediatrie|December 1, 1987
[Prognostic factors in cerebral hypoxic-ischemias in infants less than a year old]M Tardieu, D Devictor, C Wood, et al.Archives Francaises De Pediatrie|November 1, 1990
[Prognostic evaluation of severe head injuries in children]C Jeannin, E Straub, D Devictor, et al.Human Molecular Genetics|November 16, 2001
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptorN Monnier, N B Romero, J Lerale, et al.The Journal of Pediatrics|July 22, 1998
Bone marrow transplantation in metachromatic leukodystrophy caused by saposin-B deficiency: a case report with a 3-year follow-up periodP Landrieu, S Blanche, M T Vanier, et al.Neuropediatrics|August 1, 1987
Paralytic poliomyelitis in vaccinated childrenE Dussaix, G Huault, P Landrieu, et al.Revue Neurologique|January 1, 1992
[Cerebral complications of incontinentia pigmenti. A clinicopathological study of a case]C Triki, D Devictor, S Kah, et al.Journal of Neurology|May 1, 1993
Central nervous system lesions in hypomelanosis of Ito: an MRI and pathological studyV Malherbe, D Pariente, M Tardieu, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 1, 1997
[Ischemic cerebral vascular accident caused by vertebral artery dissection]B Tabarki, A el Madani, H Alvarez, et al.Pageof 12