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Dorit Lev

Showing results (31-40 of 175) with videos related to

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Journal of the Neurological Sciences|February 14, 2012
A novel mutation in the TPR6 domain of the RAPSN gene associated with congenital myasthenic syndromeEsther Leshinsky-Silver, Daniel Shapira, Keren Yosovitz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 29, 2006
Fatal outcome following foetal cerebellar haemorrhage associated with placental thrombosisGustavo Malinger, Neriman Zahalka, Dvora Kidron, et al.
Journal of Child Neurology|January 14, 2012
Dominantly inherited nonprogressive cerebellar hypoplasia identified in uteroAyelet Zerem, Yael Hacohen, Liat Ben-Sira, 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.
Journal of Child Neurology|January 25, 2013
Dominantly inherited nonprogressive cerebellar hypoplasia identified in utero: no doubtAyelet Zerem, Yael Hacohen, Liat Ben-Sira, et al.
Harefuah|March 7, 2009
[Enlargement of the fetal posterior fossa--what is the significance?]Raheli Dror, Gustavo Malinger, Liat Ben-Sira, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 17, 2008
Familial leukoencephalopathy with slowly progressive dystonia and ataxiaLubov Blumkin, Hanna Mandel, Marieta Anca-Herschkovitsch, 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 18

Showing results (31-40 of 175) with videos related to

Sort By:
Pageof 18
Journal of the Neurological Sciences|February 14, 2012
A novel mutation in the TPR6 domain of the RAPSN gene associated with congenital myasthenic syndromeEsther Leshinsky-Silver, Daniel Shapira, Keren Yosovitz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 29, 2006
Fatal outcome following foetal cerebellar haemorrhage associated with placental thrombosisGustavo Malinger, Neriman Zahalka, Dvora Kidron, et al.
Journal of Child Neurology|January 14, 2012
Dominantly inherited nonprogressive cerebellar hypoplasia identified in uteroAyelet Zerem, Yael Hacohen, Liat Ben-Sira, 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.
Journal of Child Neurology|January 25, 2013
Dominantly inherited nonprogressive cerebellar hypoplasia identified in utero: no doubtAyelet Zerem, Yael Hacohen, Liat Ben-Sira, et al.
Harefuah|March 7, 2009
[Enlargement of the fetal posterior fossa--what is the significance?]Raheli Dror, Gustavo Malinger, Liat Ben-Sira, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 17, 2008
Familial leukoencephalopathy with slowly progressive dystonia and ataxiaLubov Blumkin, Hanna Mandel, Marieta Anca-Herschkovitsch, 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 18