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Esther Leshinsky-Silver

Showing results (21-30 of 69) with videos related to

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Prenatal Diagnosis|January 21, 2003
Prenatal exclusion of Leigh syndrome due to T8993C mutation in the mitochondrial DNAEsther Leshinsky-Silver, Michal Perach, Erena Basilevsky, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Familial optic atrophy with white matter changesChana Vinkler, Dorit Lev, Hadas Kalish, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorderEsther Leshinsky-Silver, Ami Zinger, Chaim N Bibi, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 22, 2007
Evaluation of the interleukin-23 receptor gene coding variant R381Q in pediatric and adult Crohn diseaseEsther Leshinsky-Silver, Amir Karban, Ilan Dalal, et al.
Epilepsia|October 16, 2012
Resolution of epileptic encephalopathy following treatment with transdermal nicotineAyelet Zerem, Daniella Nishri, Yael Yosef, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 21, 2015
Atypical presentation of Costeff syndrome-severe psychomotor involvement and electrical status epilepticus during slow wave sleepNirit Carmi, Dorit Lev, Esther Leshinsky-Silver, et al.
Journal of the Neurological Sciences|March 17, 2015
Adult onset limb-girdle muscular dystrophy - a recessive titinopathy masquerading as myositisRon Dabby, Menachem Sadeh, David Hilton-Jones, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 19, 2014
Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorderDaniella Nishri, Simon Edvardson, Dorit Lev, et al.
The Israel Medical Association Journal : IMAJ|December 18, 2013
Association of the M3151 variant in the transient receptor potential vanilloid receptor-1 (TRPV1) gene with type 1 diabetes in an Ashkenazi Jewish populationMenachem Sadeh, Benjamin Glazer, Zohar Landau, et al.
Pediatric Research|April 28, 2006
Polymorphisms in the TNF-alpha promoter and variability in the granulomatous response in patients with Crohn's diseaseIlan Dalal, Amir Karban, Eytan Wine, et al.
Pageof 7

Showing results (21-30 of 69) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|January 21, 2003
Prenatal exclusion of Leigh syndrome due to T8993C mutation in the mitochondrial DNAEsther Leshinsky-Silver, Michal Perach, Erena Basilevsky, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Familial optic atrophy with white matter changesChana Vinkler, Dorit Lev, Hadas Kalish, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorderEsther Leshinsky-Silver, Ami Zinger, Chaim N Bibi, et al.
Journal of Pediatric Gastroenterology and Nutrition|November 22, 2007
Evaluation of the interleukin-23 receptor gene coding variant R381Q in pediatric and adult Crohn diseaseEsther Leshinsky-Silver, Amir Karban, Ilan Dalal, et al.
Epilepsia|October 16, 2012
Resolution of epileptic encephalopathy following treatment with transdermal nicotineAyelet Zerem, Daniella Nishri, Yael Yosef, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 21, 2015
Atypical presentation of Costeff syndrome-severe psychomotor involvement and electrical status epilepticus during slow wave sleepNirit Carmi, Dorit Lev, Esther Leshinsky-Silver, et al.
Journal of the Neurological Sciences|March 17, 2015
Adult onset limb-girdle muscular dystrophy - a recessive titinopathy masquerading as myositisRon Dabby, Menachem Sadeh, David Hilton-Jones, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 19, 2014
Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorderDaniella Nishri, Simon Edvardson, Dorit Lev, et al.
The Israel Medical Association Journal : IMAJ|December 18, 2013
Association of the M3151 variant in the transient receptor potential vanilloid receptor-1 (TRPV1) gene with type 1 diabetes in an Ashkenazi Jewish populationMenachem Sadeh, Benjamin Glazer, Zohar Landau, et al.
Pediatric Research|April 28, 2006
Polymorphisms in the TNF-alpha promoter and variability in the granulomatous response in patients with Crohn's diseaseIlan Dalal, Amir Karban, Eytan Wine, et al.
Pageof 7