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Showing results (51-60 of 61) with videos related to

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Voprosy Meditsinskoi Khimii|November 1, 1990

[Comparative study of human erythrocyte membranes in normal people and in Huntington's chorea patients]S F Zakharov, A M Shandala, M V Shcheglova, et al.

Genetika|September 3, 2004

[Molecular genetic analysis of hereditary neurodegenerative diseases]S N Illarioshkin, I A Ivanova-Smolenskaia, E D Markova, et al.

European Journal of Neurology|March 29, 2007

A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in RussiaS N Illarioshkin, M I Shadrina, P A Slominsky, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|August 9, 2001

[Analysis of mutations in ATP7B gene and experience with direct DNA-diagnosis in hepato-lenticular degeneration]A V Karabanov, I V Ovchinnikov, S N Illarioshkin, et al.

Journal of Neurology|July 1, 1996

Spinocerebellar ataxia type 1 in RussiaS N Illarioshkin, P A Slominsky, I V Ovchinnikov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|April 2, 2008

[A PARK8 form of Parkinson's disease: a mutational analysis of the LRRK2 gene in Russian population]M I Shadrina, S N Illarioshkin, G Kh Bagyeva, et al.

Human Molecular Genetics|June 9, 1998

De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystoniaC Klein, M F Brin, D de Leon, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|November 24, 2004

[Clinical and genetic analysis of juvenile parkinsonism in Russia]T B Zagorovskaia, S N Illarioshkin, P A Slominskiĭ, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|December 21, 2006

[7-year experience in usage of mirapex in patients with different forms of primary parkinsonism]S N Illarioshkin, I A Ivanova-Smolenskaia, T B Zagorovskaia, et al.

Brain : a Journal of Neurology|December 1, 1996

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophyS N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.

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Showing results (51-60 of 61) with videos related to

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Voprosy Meditsinskoi Khimii|November 1, 1990

[Comparative study of human erythrocyte membranes in normal people and in Huntington's chorea patients]S F Zakharov, A M Shandala, M V Shcheglova, et al.

Genetika|September 3, 2004

[Molecular genetic analysis of hereditary neurodegenerative diseases]S N Illarioshkin, I A Ivanova-Smolenskaia, E D Markova, et al.

European Journal of Neurology|March 29, 2007

A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in RussiaS N Illarioshkin, M I Shadrina, P A Slominsky, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|August 9, 2001

[Analysis of mutations in ATP7B gene and experience with direct DNA-diagnosis in hepato-lenticular degeneration]A V Karabanov, I V Ovchinnikov, S N Illarioshkin, et al.

Journal of Neurology|July 1, 1996

Spinocerebellar ataxia type 1 in RussiaS N Illarioshkin, P A Slominsky, I V Ovchinnikov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|April 2, 2008

[A PARK8 form of Parkinson's disease: a mutational analysis of the LRRK2 gene in Russian population]M I Shadrina, S N Illarioshkin, G Kh Bagyeva, et al.

Human Molecular Genetics|June 9, 1998

De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystoniaC Klein, M F Brin, D de Leon, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|November 24, 2004

[Clinical and genetic analysis of juvenile parkinsonism in Russia]T B Zagorovskaia, S N Illarioshkin, P A Slominskiĭ, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|December 21, 2006

[7-year experience in usage of mirapex in patients with different forms of primary parkinsonism]S N Illarioshkin, I A Ivanova-Smolenskaia, T B Zagorovskaia, et al.

Brain : a Journal of Neurology|December 1, 1996

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophyS N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.

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