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Natalya I. Miklina
Observed names:
N I Miklina,
N. I. Miklina,
N. Miklina,
Natalia I. Miklina,
Н.И. Миклина
Observed institution:
Research Center of Neurology
OpenAlex ID:
A5110048530
Spinocerebellar ataxia type 1 in Russia
1996
·
Sergei N. Illarioshkin
, Pyotr A. Slominsky
, et al.
·
Journal of Neurology
·
33
A common 3-bp deletion in theDYT1 gene in Russian families with early-onset torsion dystonia
1999
·
Petr A. Slominsky
, Elena D. Markova
, et al.
·
Human Mutation
·
29
Molecular Genetic Analysis of Essential Tremor
2002
·
S. N. Illarioshkin
, R. A. Rakhmonov
, et al.
·
Russian Journal of Genetics
·
22
The GTP Cyclohydrolase I Gene in Russian Families With Dopa-Responsive Dystonia
1998
·
Sergei N. Illarioshkin
, Elena D. Markova
, et al.
·
Archives of Neurology
·
18
Molecular Genetic Analysis of Hereditary Neurodegenerative Diseases
2004
·
S. N. Illarioshkin
, I. A. Ivanova-Smolenskaya
, et al.
·
Russian Journal of Genetics
·
10
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
1999
·
Elena D. Markova
, Pyotr A. Slominsky
, et al.
·
European Journal of Neurology
·
4
[Molecular-genetic analysis of torsion dystonia in Russia].
2000
·
E D Markova
, P A Slominskiĭ
, et al.
·
PubMed
·
1
[Friedreich's disease: a real spectrum of clinical manifestations in terms of direct DNA diagnosis].
1999
·
S N Illarioshkin
, E B Drizuna
, et al.
·
PubMed
·
1
[Molecular genetic testing in the diagnosis of sporadic cases of Huntington's chorea].
1998
·
I A Ivanova-Smolenskaia
, I V Ovchinnikov
, et al.
·
PubMed
·
1
Repeat expansion and phenotypic variability of Friedreich's ataxia in families of different ethnic origin from European-Asian region
1997
·
I. Ovchinnikov
, S. Illarioshkin
, et al.
·
Neuromuscular Disorders
·
1
[Presymptomatic DNA diagnosis of spinocerebellar ataxia type 1].
1997
·
S N Illarioshkin
, I A Ivanova-Smolenskaia
, et al.
·
PubMed
·
1
[The molecular genetic approach to the study of dominant spinocerebellar ataxias].
1996
·
S N Illarioshkin
, I V Ovchinnikov
, et al.
·
PubMed
·
1
[Molecular genetics of the hereditary dystonic syndromes].
2000
·
S N Illarioshkin
, E D Markova
, et al.
·
PubMed
5-29-05 DNA diagnostics in Russian families with hereditary neurological diseases
1997
·
S. Illarioshkin
, I. Ivanova-Smolenskaya
, et al.
·
Journal of the Neurological Sciences
Молекулярно-генетический подход в изучении доминантных спиноцеребеллярных атаксий
1996
·
С.Н. Иллариошкин
, И.В. Овчинников
, et al.
·
S S Korsakov Journal of Neurology and Psychiatry
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Works count:
15
Citation count:
122
H-index:
5
I10-index:
5
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