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Esther Leshinsky-Silver

Showing results (1-10 of 69) with videos related to

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Journal of Child Neurology|July 1, 2004
Should autistic children be evaluated for mitochondrial disorders?Tally Lerman-Sagie, Esther Leshinsky-Silver, Nathan Watemberg, et al.
Molecular Genetics and Metabolism|January 27, 2005
White matter involvement in mitochondrial diseasesTally Lerman-Sagie, Esther Leshinsky-Silver, Nathan Watemberg, et al.
Journal of the Neurological Sciences|July 27, 2010
MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletionsSharon Aharoni, Teres A Traves, Eldad Melamed, et al.
Journal of the Neurological Sciences|March 29, 2011
A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosumLubov Blumkin, Tally Lerman-Sagie, Dorit Lev, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 30, 2015
Painful small fiber neuropathy with gastroparesis: A new phenotype with a novel mutation in the SCN10A geneRon Dabby, Menachem Sadeh, Yelena Broitman, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
A new autosomal recessive syndrome with Zellweger-like manifestationsJoe K Ahn, Dorit Lev, Esther Leshinsky-Silver, et al.
Journal of Child Neurology|November 6, 2004
Familial hyperekplexia and refractory status epilepticus: a new autosomal recessive syndromeTally Lerman-Sagie, Nathan Watemberg, Chana Vinkler, et al.
European Journal of Medical Genetics|April 9, 2014
A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial featuresChana Vinkler, Esther Leshinsky-Silver, Marina Michelson, et al.
JIMD Reports|September 20, 2013
Heterozygous Mutations in the ADCK3 Gene in Siblings with Cerebellar Atrophy and Extreme Phenotypic VariabilityLubov Blumkin, Esther Leshinsky-Silver, Ayelet Zerem, et al.
Journal of Child Neurology|January 4, 2011
Juvenile Leigh syndrome, optic atrophy, ataxia, dystonia, and epilepsy due to T14487C mutation in the mtDNA-ND6 gene: a mitochondrial syndrome presenting from birth to adolescenceEsther Leshinsky-Silver, Ruslan Shuvalov, Shani Inbar, et al.
Pageof 7

Showing results (1-10 of 69) with videos related to

Sort By:
Pageof 7
Journal of Child Neurology|July 1, 2004
Should autistic children be evaluated for mitochondrial disorders?Tally Lerman-Sagie, Esther Leshinsky-Silver, Nathan Watemberg, et al.
Molecular Genetics and Metabolism|January 27, 2005
White matter involvement in mitochondrial diseasesTally Lerman-Sagie, Esther Leshinsky-Silver, Nathan Watemberg, et al.
Journal of the Neurological Sciences|July 27, 2010
MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletionsSharon Aharoni, Teres A Traves, Eldad Melamed, et al.
Journal of the Neurological Sciences|March 29, 2011
A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosumLubov Blumkin, Tally Lerman-Sagie, Dorit Lev, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 30, 2015
Painful small fiber neuropathy with gastroparesis: A new phenotype with a novel mutation in the SCN10A geneRon Dabby, Menachem Sadeh, Yelena Broitman, et al.
American Journal of Medical Genetics. Part A|June 5, 2003
A new autosomal recessive syndrome with Zellweger-like manifestationsJoe K Ahn, Dorit Lev, Esther Leshinsky-Silver, et al.
Journal of Child Neurology|November 6, 2004
Familial hyperekplexia and refractory status epilepticus: a new autosomal recessive syndromeTally Lerman-Sagie, Nathan Watemberg, Chana Vinkler, et al.
European Journal of Medical Genetics|April 9, 2014
A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial featuresChana Vinkler, Esther Leshinsky-Silver, Marina Michelson, et al.
JIMD Reports|September 20, 2013
Heterozygous Mutations in the ADCK3 Gene in Siblings with Cerebellar Atrophy and Extreme Phenotypic VariabilityLubov Blumkin, Esther Leshinsky-Silver, Ayelet Zerem, et al.
Journal of Child Neurology|January 4, 2011
Juvenile Leigh syndrome, optic atrophy, ataxia, dystonia, and epilepsy due to T14487C mutation in the mtDNA-ND6 gene: a mitochondrial syndrome presenting from birth to adolescenceEsther Leshinsky-Silver, Ruslan Shuvalov, Shani Inbar, et al.
Pageof 7