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Results: 1-18 |
Results: 18
MOLECULAR-GENETIC TESTING IN DIAGNOSIS OF SPORADIC CASES OF HUNTINGTONS-DISEASE
Authors: IVANOVASMOLENSKAYA IA OVCHINNIKOV IV ILLARIOSHKIN SN MARKOVA ED KLYUSHNIKOV SA NIKOLSKAYA NN MIKLINA NI
Citation: Ia. Ivanovasmolenskaya et al., MOLECULAR-GENETIC TESTING IN DIAGNOSIS OF SPORADIC CASES OF HUNTINGTONS-DISEASE, Zurnal nevropatologii i psihiatrii im. S.S. Korsakova, 98(3), 1998, pp. 19-22
THE GTP CYCLOHYDROLASE-I GENE IN RUSSIAN FAMILIES WITH DOPA-RESPONSIVE DYSTONIA
Authors: ILLARIOSHKIN SN MARKOVA ED SLOMINSKY PA MIKLINA NI POPOVA SN LIMBORSKA SA TSUJI S IVANOVASMOLENSKAYA IAI
Citation: Sn. Illarioshkin et al., THE GTP CYCLOHYDROLASE-I GENE IN RUSSIAN FAMILIES WITH DOPA-RESPONSIVE DYSTONIA, Archives of neurology, 55(6), 1998, pp. 789-792
REFINED GENETIC LOCATION OF THE CHROMOSOME 2P-LINKED PROGRESSIVE MUSCULAR-DYSTROPHY GENE
Authors: ILLARIOSHKIN SN IVANOVASMOLENSKAYA IA TANAKA H POLESHCHUK VV MARKOVA ED TSUJI S
Citation: Sn. Illarioshkin et al., REFINED GENETIC LOCATION OF THE CHROMOSOME 2P-LINKED PROGRESSIVE MUSCULAR-DYSTROPHY GENE, Genomics, 42(2), 1997, pp. 345-348
NEW FORM OF HEREDITARY ATAXIA - INBORN X- LINKED CEREBELLAR HYPOPLASIA (CLINICAL AND MOLECULAR-GENETIC ANALYSIS)
Authors: ILLARIOSHKIN SN IVANOVASMOLENSKAYA IA MARKOVA ED NIKOLSKAYA NN TSUDZI S
Citation: Sn. Illarioshkin et al., NEW FORM OF HEREDITARY ATAXIA - INBORN X- LINKED CEREBELLAR HYPOPLASIA (CLINICAL AND MOLECULAR-GENETIC ANALYSIS), Zurnal nevropatologii i psihiatrii im. S.S. Korsakova, 97(10), 1997, pp. 17-23
CLINICAL SPECTRUM AND REFINED GENETIC-MAPPING OF CHROMOSOME 2P-LINKEDAUTOSOMAL RECESSIVE PROGRESSIVE MUSCULAR-DYSTROPHY
Authors: ILLARIOSHKIN SN IVANOVASMOLENSKAYA IA TANAKA H POLESHCHUK VV TSUJI S
Citation: Sn. Illarioshkin et al., CLINICAL SPECTRUM AND REFINED GENETIC-MAPPING OF CHROMOSOME 2P-LINKEDAUTOSOMAL RECESSIVE PROGRESSIVE MUSCULAR-DYSTROPHY, Neurology, 48(3), 1997, pp. 5091-5091
PRESYMPTOMATIC DNA DIAGNOSIS OF SPINOCERE BELLAR ATAXIA TYPE-1
Authors: ILLARIOSHKIN SN IVANOVASMOLENSKAYA IA LIMBORSKAYA SA OVCHINNIKOV IV MARKOVA ED SLOMINSKII PA KLYUSHNIKOV SA MIKLINA NI
Citation: Sn. Illarioshkin et al., PRESYMPTOMATIC DNA DIAGNOSIS OF SPINOCERE BELLAR ATAXIA TYPE-1, Genetika, 33(5), 1997, pp. 693-698
LOCALIZATION OF THE AUTOSOMAL RECESSIVE M USCULAR-DYSTROPHY GENE TO CHROMOSOME 2P13 IN AN ISOLATE FROM A HIGHLAND REGION OF DAGESTAN
Authors: ILLARIOSHKIN SN IVANOVASMOLENSKAYA IA LIMBORSKAYA SA POLESHCHUK VV MARKOVA ED SLOMINSKII PA BULAEVA KB TSUJI S
Citation: Sn. Illarioshkin et al., LOCALIZATION OF THE AUTOSOMAL RECESSIVE M USCULAR-DYSTROPHY GENE TO CHROMOSOME 2P13 IN AN ISOLATE FROM A HIGHLAND REGION OF DAGESTAN, Genetika, 33(11), 1997, pp. 1551-1558
SEARCHING FOR MODIFIER GENE(S) IN LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE2B AND MIYOSHI-MYOPATHY
Authors: FRANZMANN TL GREENBERG CR ILLARIOSHKIN SN IVANOVASMOLENSKAYA IA MORGAN K WEILER T NYLEN E WROGEMANN K
Citation: Tl. Franzmann et al., SEARCHING FOR MODIFIER GENE(S) IN LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE2B AND MIYOSHI-MYOPATHY, American journal of human genetics, 61(4), 1997, pp. 1602-1602
MUTATION SCREENING IN RUSSIAN FAMILIES WITH DOPA-RESPONSIVE DYSTONIA
Authors: ILLARIOSHKIN SN MIKLINA NI SLOMINSKY PA MARKOVA ED LIMBORSKA SA TSUJI S IVANOVASMOLENSKAYA IA
Citation: Sn. Illarioshkin et al., MUTATION SCREENING IN RUSSIAN FAMILIES WITH DOPA-RESPONSIVE DYSTONIA, American journal of human genetics, 61(4), 1997, pp. 1962-1962
X-LINKED NONPROGRESSIVE CONGENITAL CEREBELLAR HYPOPLASIA - CLINICAL DESCRIPTION AND MAPPING TO CHROMOSOME XQ
Authors: ILLARIOSHKIN SN TANAKA H MARKOVA ED NIKOLSKAYA NN IVANOVASMOLENSKAYA IA TSUJI S
Citation: Sn. Illarioshkin et al., X-LINKED NONPROGRESSIVE CONGENITAL CEREBELLAR HYPOPLASIA - CLINICAL DESCRIPTION AND MAPPING TO CHROMOSOME XQ, Annals of neurology, 40(1), 1996, pp. 75-83
SPINOCEREBELLAR ATAXIA TYPE-1 IN RUSSIA
Authors: ILLARIOSHKIN SN SLOMINSKY PA OVCHINNIKOV IV MARKOVA ED MIKLINA NI KLYUSHNIKOV SA SHADRINA M VERESHCHAGIN NV LIMBORSKAYA SA IVANOVASMOLENSKAYA IA
Citation: Sn. Illarioshkin et al., SPINOCEREBELLAR ATAXIA TYPE-1 IN RUSSIA, Journal of neurology, 243(7), 1996, pp. 506-510
MOLECULAR-GENETIC APPROACH TO INVESTIGATION OF DOMINANT SPINOCEREBELLAR ATAXIAS
Authors: ILLARIOSHKIN SN OVCHINNIKOV IV IVANOVASMOLENSKAYA IA VERESCHAGIN NV MARKOVA ED MIKLINA NI KLUSHNIKOV SA
Citation: Sn. Illarioshkin et al., MOLECULAR-GENETIC APPROACH TO INVESTIGATION OF DOMINANT SPINOCEREBELLAR ATAXIAS, Zurnal nevropatologii i psihiatrii im. S.S. Korsakova, 96(1), 1996, pp. 37-41
X-LINKED CONGENITAL CEREBELLAR HYPOPLASIA - CLINICAL DESCRIPTION OF ANOVEL HEREDITARY SYNDROME AND LINKAGE TO THE PERICENTROMERIC REGION OF CHROMOSOME-X
Authors: ILLARIOSHKIN SN TANAKA H MARKOVA ED IVANOVASMOLENSKAYA IA TSUJI S
Citation: Sn. Illarioshkin et al., X-LINKED CONGENITAL CEREBELLAR HYPOPLASIA - CLINICAL DESCRIPTION OF ANOVEL HEREDITARY SYNDROME AND LINKAGE TO THE PERICENTROMERIC REGION OF CHROMOSOME-X, Neurology, 46(2), 1996, pp. 2097-2097
ANALYSIS OF TRINUCLEOTIDE REPEAT EXPANSIO N AS A NEW MECHANISM OF MUTATION IN HUNTINGTONS-CHOREA - THEORETICAL AND APPLIED ASPECTS
Authors: ILLARIOSHKIN SN IVANOVASMOLENSKAYA IA MARKOVA ED NIKOLSKAYA NN CHABRASHVILI TZ INSAROVA NG
Citation: Sn. Illarioshkin et al., ANALYSIS OF TRINUCLEOTIDE REPEAT EXPANSIO N AS A NEW MECHANISM OF MUTATION IN HUNTINGTONS-CHOREA - THEORETICAL AND APPLIED ASPECTS, Genetika, 32(1), 1996, pp. 103-109
CLINICAL AND MOLECULAR ANALYSIS OF A LARGE FAMILY WITH 3 DISTINCT PHENOTYPES OF PROGRESSIVE MUSCULAR-DYSTROPHY
Authors: ILLARIOSHKIN SN IVANOVASMOLENSKAYA IA TANAKA H VERESHCHAGIN NV MARKOVA ED POLESHCHUK VV LOZHNIKOVA SM SUKHORUKOV VS LIMBORSKA SA SLOMINSKY PA BULAYEVA KB TSUJI S
Citation: Sn. Illarioshkin et al., CLINICAL AND MOLECULAR ANALYSIS OF A LARGE FAMILY WITH 3 DISTINCT PHENOTYPES OF PROGRESSIVE MUSCULAR-DYSTROPHY, Brain, 119, 1996, pp. 1895-1909
ANALYSIS OF TRIPLET EXPANSION - NEW MOLEC ULAR-GENETIC METHOD OF INVESTIGATION OF MUTATION MESSIANISM IN NEUROGENETICS (HUNTINGTONS-CHOREA)
Authors: IVANOVASMOLENSKAYA IA VERESCHAGIN NV ILLARIOSHKIN SN MARKOVA ED NIKOLSKAYA NN CHABRASHVILI TZ INSAROVA NG
Citation: Ia. Ivanovasmolenskaya et al., ANALYSIS OF TRIPLET EXPANSION - NEW MOLEC ULAR-GENETIC METHOD OF INVESTIGATION OF MUTATION MESSIANISM IN NEUROGENETICS (HUNTINGTONS-CHOREA), Zurnal nevropatologii i psihiatrii im. S.S. Korsakova, 95(1), 1995, pp. 52-57
NOVEL MUTATIONAL MECHANISM IN MAN - EXPAN SION OF TRINUCLEOTIDE REPEATS
Authors: ILLARIOSHKIN SN IVANOVASMOLENSKAYA IA MARKOVA ED
Citation: Sn. Illarioshkin et al., NOVEL MUTATIONAL MECHANISM IN MAN - EXPAN SION OF TRINUCLEOTIDE REPEATS, Genetika, 31(11), 1995, pp. 1478-1489
TRINUCLEOTIDE REPEAT LENGTH AND RATE OF PROGRESSION OF HUNTINGTONS-DISEASE
Authors: ILLARIOSHKIN SN IGARASHI S ONODERA O MARKOVA ED NIKOLSKAYA NN TANAKA H CHABRASHWILI TZ INSAROVA NG ENDO K IVANOVASMOLENSKAYA IA TSUJI S
Citation: Sn. Illarioshkin et al., TRINUCLEOTIDE REPEAT LENGTH AND RATE OF PROGRESSION OF HUNTINGTONS-DISEASE, Annals of neurology, 36(4), 1994, pp. 630-635
Risultati: 1-18 |