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Harefuah
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July 7, 2000
[Mitochondrial diseases: molecular genetics and clinical applications]
E Leshinsky-Silver, D Lev, T Lerman-Sagie
Hearing Research
|
April 7, 2005
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness
E Leshinsky-Silver, Z Berman, C Vinkler, et al.
Human Genetics
|
June 29, 2007
Gene symbol: GJB2
E Leshinsky-Silver, Z Berman, C Vinkler, et al.
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 mutation
D 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 gene
E Leshinsky-Silver, M Ginzberg, R Dabby, et al.
Journal of Inherited Metabolic Disease
|
November 1, 2002
Reversible fulminant lactic acidosis and liver failure in an infant with hepatic cytochrome-c oxidase deficiency
D Lev, E Gilad, E Leshinsky-Silver, et al.
International Journal of Colorectal Disease
|
March 3, 2007
Lack of association of the 3'-UTR polymorphism in the NFKBIA gene with Crohn's disease in an Israeli cohort
E Leshinsky-Silver, A Karban, S Cohen, 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 depletion
E Leshinsky-Silver, M Michelson, S Cohen, et al.
Journal of Inherited Metabolic Disease
|
April 5, 2001
Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenone
T Lerman-Sagie, P Rustin, D Lev, et al.
Biochemical and Biophysical Research Communications
|
July 19, 2005
Fulminant neurological deterioration in a neonate with Leigh syndrome due to a maternally transmitted missense mutation in the mitochondrial ND3 gene
E Leshinsky-Silver, D Lev, Z Tzofi-Berman, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Harefuah
|
July 7, 2000
[Mitochondrial diseases: molecular genetics and clinical applications]
E Leshinsky-Silver, D Lev, T Lerman-Sagie
Hearing Research
|
April 7, 2005
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness
E Leshinsky-Silver, Z Berman, C Vinkler, et al.
Human Genetics
|
June 29, 2007
Gene symbol: GJB2
E Leshinsky-Silver, Z Berman, C Vinkler, et al.
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 mutation
D 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 gene
E Leshinsky-Silver, M Ginzberg, R Dabby, et al.
Journal of Inherited Metabolic Disease
|
November 1, 2002
Reversible fulminant lactic acidosis and liver failure in an infant with hepatic cytochrome-c oxidase deficiency
D Lev, E Gilad, E Leshinsky-Silver, et al.
International Journal of Colorectal Disease
|
March 3, 2007
Lack of association of the 3'-UTR polymorphism in the NFKBIA gene with Crohn's disease in an Israeli cohort
E Leshinsky-Silver, A Karban, S Cohen, 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 depletion
E Leshinsky-Silver, M Michelson, S Cohen, et al.
Journal of Inherited Metabolic Disease
|
April 5, 2001
Dramatic improvement in mitochondrial cardiomyopathy following treatment with idebenone
T Lerman-Sagie, P Rustin, D Lev, et al.
Biochemical and Biophysical Research Communications
|
July 19, 2005
Fulminant neurological deterioration in a neonate with Leigh syndrome due to a maternally transmitted missense mutation in the mitochondrial ND3 gene
E Leshinsky-Silver, D Lev, Z Tzofi-Berman, et al.
Page
of 2