I A Ivanova-Smolenskaya - JoVE Visualize

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Bulletin of Experimental Biology and Medicine|January 10, 2002

Peculiarities of carnosine metabolism in a patient with pronounced homocarnosinemiaG G Kramarenko, E D Markova, I A Ivanova-Smolenskaya, et al.

Annals of Neurology|July 1, 1996

X-linked nonprogressive congenital cerebellar hypoplasia: clinical description and mapping to chromosome XqS N Illarioshkin, H Tanaka, E D Markova, et al.

Genomics|June 1, 1997

Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy geneS N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.

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.

Bulletin of Experimental Biology and Medicine|December 18, 2010

Therapeutic efficacy of the neuroprotective plant adaptogen in neurodegenerative disease (Parkinson's disease as an example)E V Bocharov, I A Ivanova-Smolenskaya, V V Poleshchuk, et al.

Neuroscience and Behavioral Physiology|September 17, 2004

Characteristics of learning voluntary control of posture in lesions of the pyramidal and nigrostriatal systemsM E Ioffe, K I Ustinova, L A Chernikova, 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.

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.

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.

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Showing results (1-10 of 19) with videos related to

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Bulletin of Experimental Biology and Medicine|January 10, 2002

Peculiarities of carnosine metabolism in a patient with pronounced homocarnosinemiaG G Kramarenko, E D Markova, I A Ivanova-Smolenskaya, et al.

Annals of Neurology|July 1, 1996

X-linked nonprogressive congenital cerebellar hypoplasia: clinical description and mapping to chromosome XqS N Illarioshkin, H Tanaka, E D Markova, et al.

Genomics|June 1, 1997

Refined genetic location of the chromosome 2p-linked progressive muscular dystrophy geneS N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.

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.

Bulletin of Experimental Biology and Medicine|December 18, 2010

Therapeutic efficacy of the neuroprotective plant adaptogen in neurodegenerative disease (Parkinson's disease as an example)E V Bocharov, I A Ivanova-Smolenskaya, V V Poleshchuk, et al.

Neuroscience and Behavioral Physiology|September 17, 2004

Characteristics of learning voluntary control of posture in lesions of the pyramidal and nigrostriatal systemsM E Ioffe, K I Ustinova, L A Chernikova, 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.

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.

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.

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