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D Markova

Showing results (111-120 of 146) with videos related to

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Journal of Medical Genetics|March 2, 1999
The His1069Gln mutation in the ATP7B gene in Russian patients with Wilson diseaseI A Ivanova-Smolenskaya, I V Ovchinnikov, A V Karabanov, 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.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|January 1, 1995
[Triplet expansion analysis--a new molecular genetic method for studying the mechanism of mutations in neurogenetics (exemplified by Huntington chorea)]I A Ivanova-Smolenskaia, N V Vereshchagin, S N Illarioshkin, et al.
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.
Pageof 15

Showing results (111-120 of 146) with videos related to

Sort By:
Pageof 15
Journal of Medical Genetics|March 2, 1999
The His1069Gln mutation in the ATP7B gene in Russian patients with Wilson diseaseI A Ivanova-Smolenskaya, I V Ovchinnikov, A V Karabanov, 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.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|January 1, 1995
[Triplet expansion analysis--a new molecular genetic method for studying the mechanism of mutations in neurogenetics (exemplified by Huntington chorea)]I A Ivanova-Smolenskaia, N V Vereshchagin, S N Illarioshkin, et al.
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.
Pageof 15