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Voprosy Meditsinskoi Khimii
|
October 1, 1996
[Search for expansion of CAG-repeats in DNA sequences expressed in the brain of humans with psychiatric and neurological diseases]
I V Ovchinnikov, E A Braga, M G Aksenova, et al.
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 Russia
S 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 Russia
S 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.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 31, 2003
Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism
Sergei N Illarioshkin, Magali Periquet, Nina Rawal, 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 dystonia
C 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.
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Search research articles
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Showing results (131-140 of 146) with videos related to
Sort By:
Page
of 15
Voprosy Meditsinskoi Khimii
|
October 1, 1996
[Search for expansion of CAG-repeats in DNA sequences expressed in the brain of humans with psychiatric and neurological diseases]
I V Ovchinnikov, E A Braga, M G Aksenova, et al.
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 Russia
S 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 Russia
S 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.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 31, 2003
Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism
Sergei N Illarioshkin, Magali Periquet, Nina Rawal, 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 dystonia
C 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.
Page
of 15