E D Markova - JoVE Visualize

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Neurology|January 3, 2001

Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathyS N Illarioshkin, I A Ivanova-Smolenskaya, C R Greenberg, et al.

Journal of Neurology|February 1, 2000

Studies of the candidate genes in X-linked congenital cerebellar hypoplasiaS N Illarioshkin, K M Allen, J G Gleeson, et al.

Zhurnal Nevropatologii I Psikhiatrii Imeni S.S. Korsakova (Moscow, Russia : 1952)|January 1, 1990

[Clinico-immunologic correlations and various characteristics of the lymphocyte receptors in hepatocerebral dystrophy]I V Gannushkina, I G Zhirnova, A Chlonkovska, et al.

Genetika|February 11, 2003

[Molecular genetic analysis of essential tremor]S N Illarioshkin, R A Rakhmonov, I A Ivanova-Smolenskaia, et al.

Archives of Neurology|June 17, 1998

The GTP cyclohydrolase I gene in Russian families with dopa-responsive dystoniaS N Illarioshkin, E D Markova, P A Slominsky, et al.

Genetika|February 28, 1998

[Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13]S N Illarioshkin, I A Ivanova-Smolenskaia, S A Dimborskaia, et al.

Genetika|May 1, 1997

[Presymptomatic DNA diagnosis of spinocerebellar ataxia type 1]S N Illarioshkin, I A Ivanova-Smolenskaia, S A Limborskaia, et al.

Genetika|September 20, 2000

[Molecular-genetic analysis of torsion dystonia in Russia]E D Markova, P A Slominskiĭ, S N Illarioshkin, et al.

Annals of Neurology|October 1, 1994

Trinucleotide repeat length and rate of progression of Huntington's diseaseS N Illarioshkin, S Igarashi, O Onodera, et al.

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.

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Showing results (41-50 of 61) with videos related to

Sort By:

Pageof 7

Neurology|January 3, 2001

Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathyS N Illarioshkin, I A Ivanova-Smolenskaya, C R Greenberg, et al.

Journal of Neurology|February 1, 2000

Studies of the candidate genes in X-linked congenital cerebellar hypoplasiaS N Illarioshkin, K M Allen, J G Gleeson, et al.

Zhurnal Nevropatologii I Psikhiatrii Imeni S.S. Korsakova (Moscow, Russia : 1952)|January 1, 1990

[Clinico-immunologic correlations and various characteristics of the lymphocyte receptors in hepatocerebral dystrophy]I V Gannushkina, I G Zhirnova, A Chlonkovska, et al.

Genetika|February 11, 2003

[Molecular genetic analysis of essential tremor]S N Illarioshkin, R A Rakhmonov, I A Ivanova-Smolenskaia, et al.

Archives of Neurology|June 17, 1998

The GTP cyclohydrolase I gene in Russian families with dopa-responsive dystoniaS N Illarioshkin, E D Markova, P A Slominsky, et al.

Genetika|February 28, 1998

[Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13]S N Illarioshkin, I A Ivanova-Smolenskaia, S A Dimborskaia, et al.

Genetika|May 1, 1997

[Presymptomatic DNA diagnosis of spinocerebellar ataxia type 1]S N Illarioshkin, I A Ivanova-Smolenskaia, S A Limborskaia, et al.

Genetika|September 20, 2000

[Molecular-genetic analysis of torsion dystonia in Russia]E D Markova, P A Slominskiĭ, S N Illarioshkin, et al.

Annals of Neurology|October 1, 1994

Trinucleotide repeat length and rate of progression of Huntington's diseaseS N Illarioshkin, S Igarashi, O Onodera, et al.

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.

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