Zobrazeno 1 - 4
of 4
pro vyhledávání: '"T. B. Zagorovskaya"'
Autor:
S. N. Illarioshkin, P. A. Slominsky, M. I. Shadrina, G. Kh. Bagyeva, T. B. Zagorovskaya, E. D. Markova, A. V. Karabanov, V. V. Poleshchuk, E. V. Polevaya, N. V. Fedorova, S. A. Limborskaya, I. A. Ivanova-Smolenskaya
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 1, Iss 1, Pp 23-31 (2007)
We performed search for mutations in the LRRK2, PRKN (parkin)and SNCA (a-synuclein) genes in 359 patients of Slavonic ethnicorigin (169 men and 190 women) with Parkinsons disease, ofwhom 345 represented sporadic cases. Age at the disease onset wasfro
Externí odkaz:
https://doaj.org/article/eea0e4fea6f94c35b934597007f0b95d
Autor:
Sergey N. Illarioshkin, Markova Ed, M. I. Shadrina, T. B. Zagorovskaya, Miklina Ni, Irina A. Ivanova-Smolenskaya, Svetlana A. Limborska, S. A. Klyushnikov, P. A. Slominsky
Publikováno v:
Russian Journal of Genetics. 40:663-671
The review summarizes the results of a decade of molecular genetic studies of several high-incidence hereditary neurodegenerative diseases, including primary parkinsonism, various forms of hereditary dystonia and ataxia, polyglutamine disorders, hepa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af4fedf9ec41aebfbf9f4dfa2fb94cd2
https://doi.org/10.1023/b:ruge.0000033314.49573.db
https://doi.org/10.1023/b:ruge.0000033314.49573.db
Autor:
G. Kh. Bagyeva, Maria Shadrina, Markova Ed, T. B. Zagorovskaya, E. V. Bespalova, Irina A. Ivanova-Smolenskaya, Petr Slominsky, Svetlana A. Limborska, Sergey N. Illarioshkin
Publikováno v:
European journal of neurology. 14(4)
A PARK8 form of Parkinson's disease (PD) is caused by a novel gene, leucine-rich repeat kinase 2 (LRRK2), and a single mutation G2019S was found in a proportion of LRRK2-associated cases of diverse ethnic origins. We performed the LRRK2 G2019S mutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4b6aa3e52c47bfc0ebc5cccbba2b705
https://pubmed.ncbi.nlm.nih.gov/17388990
https://pubmed.ncbi.nlm.nih.gov/17388990
Lack of α-synuclein gene mutations in families with autosomal dominant Parkinson's disease in Russia
Autor:
Sergei N. Illarioshkin, Irina A. Ivanova-Smolenskaya, Alexis Brice, Markova Ed, T. B. Zagorovskaya
Publikováno v:
Journal of Neurology. 247:968-969
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5542f93df5458375f123fefc79868f77
https://doi.org/10.1007/s004150070056
https://doi.org/10.1007/s004150070056