E D Markova - JoVE Visualize

Showing results (31-40 of 61) with videos related to

Pageof 7

Sort By:

European Journal of Neurology|October 29, 2000

Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical featuresS N Illarioshkin, G K Bagieva, S A Klyushnikov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|November 20, 2001

[Nervous tissue protein autoantibodies in hepatolenticular degeneration]S G Morozov, M P Usanova, V V Poleshchuk, et al.

Genetika|January 1, 1996

[Analysis of trinucleotide repeat expansion as a new mechanism of mutation in Huntington's chorea: theoretical and applied aspects]S N Illarioshkin, I A Ivanova-Smolenskaia, E D Markova, et al.

Voprosy Meditsinskoi Khimii|January 1, 1997

[Immunochemical correlates of the severity of Parkinson's disease]S G Morozov, I A Ivanova-Smolenskaia, E D Markova, et al.

Human Mutation|September 8, 1999

A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystoniaP A Slominsky, E D Markova, M I Shadrina, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 7, 2000

[Friedreich's disease: a real spectrum of clinical manifestations in terms of direct DNA diagnosis]S N Illarioshkin, E B Drizuna, G Kh Bagieva, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|January 1, 1996

[The molecular genetic approach to the study of dominant spinocerebellar ataxias]S N Illarioshkin, I V Ovchinnikov, I A Ivanova-Smolenskaia, et al.

Laboratornoe Delo|January 1, 1989

[Ceruloplasmin activity in the blood during progressive diseases of the central nervous system]T I Mzhel'skaia, I A Zavalishin, I A Ivanova-Smolenskaia, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|May 12, 1998

[Molecular genetic testing in the diagnosis of sporadic cases of Huntington's chorea]I A Ivanova-Smolenskaia, I V Ovchinnikov, S N Illarioshkin, et al.

European Journal of Neurology|August 24, 1999

A novel mutation in the GTP cyclohydrolase I gene associated with a broad range of clinical presentations in a family with autosomal dominant dopa-responsive dystoniaE D Markova, P A Slominsky, S N Illarioshkin, et al.

Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:

Pageof 7

European Journal of Neurology|October 29, 2000

Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical featuresS N Illarioshkin, G K Bagieva, S A Klyushnikov, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|November 20, 2001

[Nervous tissue protein autoantibodies in hepatolenticular degeneration]S G Morozov, M P Usanova, V V Poleshchuk, et al.

Genetika|January 1, 1996

[Analysis of trinucleotide repeat expansion as a new mechanism of mutation in Huntington's chorea: theoretical and applied aspects]S N Illarioshkin, I A Ivanova-Smolenskaia, E D Markova, et al.

Voprosy Meditsinskoi Khimii|January 1, 1997

[Immunochemical correlates of the severity of Parkinson's disease]S G Morozov, I A Ivanova-Smolenskaia, E D Markova, et al.

Human Mutation|September 8, 1999

A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystoniaP A Slominsky, E D Markova, M I Shadrina, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|October 7, 2000

[Friedreich's disease: a real spectrum of clinical manifestations in terms of direct DNA diagnosis]S N Illarioshkin, E B Drizuna, G Kh Bagieva, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|January 1, 1996

[The molecular genetic approach to the study of dominant spinocerebellar ataxias]S N Illarioshkin, I V Ovchinnikov, I A Ivanova-Smolenskaia, et al.

Laboratornoe Delo|January 1, 1989

[Ceruloplasmin activity in the blood during progressive diseases of the central nervous system]T I Mzhel'skaia, I A Zavalishin, I A Ivanova-Smolenskaia, et al.

Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|May 12, 1998

[Molecular genetic testing in the diagnosis of sporadic cases of Huntington's chorea]I A Ivanova-Smolenskaia, I V Ovchinnikov, S N Illarioshkin, et al.

European Journal of Neurology|August 24, 1999

A novel mutation in the GTP cyclohydrolase I gene associated with a broad range of clinical presentations in a family with autosomal dominant dopa-responsive dystoniaE D Markova, P A Slominsky, S N Illarioshkin, et al.

Pageof 7