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Journal of Neurology
|
February 1, 2000
Studies of the candidate genes in X-linked congenital cerebellar hypoplasia
S 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.
Folia Biologica
|
April 19, 2022
Prostaglandin F2α Causes Fast Degenerative Changes in Ovulated Mouse Oocytes
A I Kolarov, V P Hadzhinesheva, I V Chakarova, 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 dystonia
S 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.
Anatomical Record (Hoboken, N.J. : 2007)
|
June 3, 2009
Aged human thymus hassall's corpuscles are immunoreactive for IGF-I and IGF-I receptor
Tsvetana Ts Marinova, Lyubomir D Spassov, Veselin I Vlassov, 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 disease
S N Illarioshkin, S Igarashi, O Onodera, et al.
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Search research articles
Search
Showing results (121-130 of 146) with videos related to
Sort By:
Page
of 15
Journal of Neurology
|
February 1, 2000
Studies of the candidate genes in X-linked congenital cerebellar hypoplasia
S 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.
Folia Biologica
|
April 19, 2022
Prostaglandin F2α Causes Fast Degenerative Changes in Ovulated Mouse Oocytes
A I Kolarov, V P Hadzhinesheva, I V Chakarova, 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 dystonia
S 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.
Anatomical Record (Hoboken, N.J. : 2007)
|
June 3, 2009
Aged human thymus hassall's corpuscles are immunoreactive for IGF-I and IGF-I receptor
Tsvetana Ts Marinova, Lyubomir D Spassov, Veselin I Vlassov, 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 disease
S N Illarioshkin, S Igarashi, O Onodera, et al.
Page
of 15