Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism
Illarioshkin, Sergei N., Periquet, Magali, Rawal, Nina, Lücking, Christoph B., Zagorovskaya, Tatyana B., Slominsky, Pyotr A., Miloserdova, Olga V., Markova, Elena D., Limborska, Svetlana A., Ivanova-Smolenskaya, Irina A., Brice, Alexis
Published in Movement disorders (01.08.2003)
Published in Movement disorders (01.08.2003)
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Nikolai V. Konovalov (1900-1966): His Role in the Development of Neurology and the Creation of the Institute of Neurology of the Russian Academy of Medical Sciences
Ivanova-Smolenskaya, Irina A., Markova, Elena D.
Published in Journal of the history of the neurosciences (01.01.2007)
Published in Journal of the history of the neurosciences (01.01.2007)
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A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia
Slominsky, Petr A., Markova, Elena D., Shadrina, Marya I., Illarioshkin, Sergey N., Miklina, Natalia I., Limborska, Svetlana A., Ivanova-Smolenskaya, Irina A.
Published in Human mutation (1999)
Published in Human mutation (1999)
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Clinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan
Illarioshkin, Sergei N., Ivanova-Smolenskaya, Irina A., Rahmonov, Rahmatullo A., Markova, Elena D., Stevanin, Giovanni, Brice, Alexis
Published in Movement disorders (01.09.2000)
Published in Movement disorders (01.09.2000)
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Refined Genetic Location of the Chromosome 2p-Linked Progressive Muscular Dystrophy Gene
Illarioshkin, Sergei N., Ivanova-Smolenskaya, Irina A., Tanaka, Hajime, Poleshchuk, Vsevolod V., Markova, Elena D., Tsuji, Shoji
Published in Genomics (San Diego, Calif.) (01.06.1997)
Published in Genomics (San Diego, Calif.) (01.06.1997)
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The GTP Cyclohydrolase I Gene in Russian Families With Dopa-Responsive Dystonia
Illarioshkin, Sergei N, Markova, Elena D, Slominsky, Pyotr A, Miklina, Natalya I, Popova, Svetlana N, Limborska, Svetlana A, Tsuji, Shoji, Ivanova-Smolenskaya, Irina A
Published in Archives of neurology (Chicago) (01.06.1998)
Published in Archives of neurology (Chicago) (01.06.1998)
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De Novo Mutations (GAG Deletion) in the DYT1 Gene in Two Non-Jewish Patients with Early-onset Dystonia
Klein, Christine, Brin, Mitchell F., de Leon, Deborah, Limborska, Svetlana A., Ivanova-Smolenskaya, Irina A., Bressman, Susan B., Friedman, Andrzej, Markova, Elena D., Risch, Neil J., Breakefield, Xandra O., Ozelius, Laurie J.
Published in Human molecular genetics (01.07.1998)
Published in Human molecular genetics (01.07.1998)
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Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium
Ozelius, L J, Hewett, J, Kramer, P, Bressman, S B, Shalish, C, de Leon, D, Rutter, M, Risch, N, Brin, M F, Markova, E D, Limborska, S A, Ivanova-Smolenskaya, I A, McCormick, M K, Fahn, S, Buckler, A J, Gusella, J F, Breakefield, X O
Published in Genome research (01.05.1997)
Published in Genome research (01.05.1997)
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Trinucleotide repeat length and rate of progression of Huntington's disease
Illarioshkin, S N, Igarashi, S, Onodera, O, Markova, E D, Nikolskaya, N N, Tanaka, H, Chabrashwili, T Z, Insarova, N G, Endo, K, Ivanova-Smolenskaya, I A
Published in Annals of neurology (01.10.1994)
Published in Annals of neurology (01.10.1994)
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The His1069Gln mutation in the ATP7B gene in Russian patients with Wilson disease
IVANOVA-SMOLENSKAYA, IRINA A, OVCHINNIKOV, IGOR V, KARABANOV, ALEXEY V, DEINEKO, NATALYA L, POLESHCHUK, VSEVOLOD V, MARKOVA, ELENA D, ILLARIOSHKIN, SERGEI N
Published in Journal of medical genetics (01.02.1999)
Published in Journal of medical genetics (01.02.1999)
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Alcohol dehydrogenase alleles in Parkinson's disease
Buervenich, Silvia, Sydow, Olof, Carmine, Andrea, Zhang, Zhiping, Anvret, Maria, Olson, Lars
Published in Movement disorders (01.09.2000)
Published in Movement disorders (01.09.2000)
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A common 3-bp deletion in theDYT1 gene in Russian families with early-onset torsion dystonia
Slominsky, Petr A., Markova, Elena D., Shadrina, Marya I., Illarioshkin, Sergey N., Miklina, Natalia I., Limborska, Svetlana A., Ivanova-Smolenskaya, Irina A.
Published in Human mutation (1999)
Published in Human mutation (1999)
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Studies of the candidate genes in X-linked congenital cerebellar hypoplasia
Illarioshkin, S N, Allen, K M, Gleeson, J G, Tsuji, S, Ikeuchi, T, Markova, E D, Walsh, C A, Ivanova-Smolenskaya, I A
Published in Journal of neurology (01.12.1999)
Published in Journal of neurology (01.12.1999)
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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 dystonia
Markova, Elena D., Slominsky, Pyotr A., Illarioshkin, Sergei N., Miklina, Natalya I., Popova, Svetlana N., Limborska, Svetlana A., Ivanova-Smolenskaya, Irina A.
Published in European journal of neurology (01.09.1999)
Published in European journal of neurology (01.09.1999)
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Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism
ILLARIOSHKIN, Sergei N, PERIQUET, Magali, BRICE, Alexis, RAWAL, Nina, LÜCKING, Christoph B, ZAGOROVSKAYA, Tatyana B, SLOMINSKY, Pyotr A, MILOSERDOVA, Olga V, MARKOVA, Elena D, LIMBORSKA, Svetlana A, IVANOVA-SMOLENSKAYA, Irina A
Published in Movement disorders (2003)
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Published in Movement disorders (2003)
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Spinocerebellar ataxia type 1 in Russia
Illarioshkin, S N, Slominsky, P A, Ovchinnikov, I V, Markova, E D, Miklina, N I, Klyushnikov, S A, Shadrina, M, Vereshchagin, N V, Limborskaya, S A, Ivanova-Smolenskaya, I A
Published in Journal of neurology (01.07.1996)
Published in Journal of neurology (01.07.1996)
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