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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 9, 2002
White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutationD Lev, M Yanoov-Sharav, N Watemberg, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 18, 2012
Neonatal vocal cord paralysis-an early presentation of hereditary neuralgic amyotrophy due to a mutation in the SEPT9 geneE Leshinsky-Silver, M Ginzberg, R Dabby, et al.Journal of Child Neurology|January 21, 2000
Neurologic presentations of mitochondrial disordersA Nissenkorn, A Zeharia, D Lev, et al.Journal of Child Neurology|December 30, 1999
Phenobarbital still has a role in epilepsy treatmentT Lerman-Sagie, P LermanHarefuah|July 26, 2000
[Ketogenic diet--an alternative therapy for epilepsy in adults]Y Schiff, T Lerman-SagieHuman Genetics|May 14, 1999
Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier motherS M Tanner, K H Orstavik, M Kristiansen, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 24, 2007
A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletionE Leshinsky-Silver, M Michelson, S Cohen, et al.European Journal of Radiology|January 3, 2006
Normal and abnormal fetal brain development during the third trimester as demonstrated by neurosonographyG Malinger, D Lev, T Lerman-SagieDevelopmental Medicine and Child Neurology|March 1, 1991
Effect of early corticosteroid therapy for Landau-Kleffner syndromeP Lerman, T Lerman-Sagie, S KivityPageof 20