Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Irina A. Ivanova-Smolenskaya"'
Autor:
Gulbakhar Bagyeva, Sergei N. Illarioshkin, Maria Shadrina, Elena V. Semenova, Irina A. Ivanova-Smolenskaya, P. A. Slominsky, Svetlana A. Limborska
Publikováno v:
Movement Disorders. 27:139-143
Background: Deletions and duplications of single exons or exon groups account for a large proportion of the PARK2 gene mutations described in juvenile autosomal recessive Parkinson’s disease (PD). Methods: We analyzed rearrangements in exons 1 to 1
Autor:
Elena V. Filatova, Svetlana A. Limborska, Irina A. Ivanova-Smolenskaya, Sergey N. Illarioshkin, Petr Slominsky, A. V. Karabanov, Maria Shadrina
Publikováno v:
Molecular Biology. 45:417-420
Parkinson’s disease (PD) is the second most common progressive neurodegenerative disorder characterized by the degeneration of dopaminergic neurons. Detecting changes in gene expression in untreated de novo patients with PD is important for underst
Publikováno v:
Journal of the History of the Neurosciences. 16:160-167
Nikolai V. Konovalov (1900-1966) has left a significant imprint in the history of Russian neuroscience. He was among the coryphaei of international and national neurology. Along with the large number of fundamental scientific papers that have determi
Autor:
Petr Slominsky, Irina A. Ivanova-Smolenskaya, Sergei N. Illarioshkin, Svetlana A. Limborska, Elena V. Filatova, Ekaterina Yu. Fedotova, Maria Shadrina
Publikováno v:
Advances in Parkinson's Disease. :28-30
Background: Parkinson’s disease (PD) is caused by complex interactions between genetic and environmental factors. Mendelian forms of PD rarely occur in practice, but respective genes may play some role in pathogenesis of a common sporadic form of t
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
Autor:
Olga V. Miloserdova, Irina A. Ivanova-Smolenskaya, Magali Periquet, P. A. Slominsky, Tatyana B. Zagorovskaya, Sergei N. Illarioshkin, Alexis Brice, Markova Ed, Christoph B. Lücking, Nina Rawal, Svetlana A. Limborska
Publikováno v:
Movement Disorders. 18:914-919
Autosomal recessive juvenile parkinsonism (AR-JP) is a form of hereditary parkinsonism characterized by variable clinical presentations and caused by mutations in a novel gene, parkin, on chromosome 6q25.2–27. Until now, no Russian cases of parkin-
Autor:
Alexis Brice, Sergey N. Illarioshkin, Markova Ed, Irina A. Ivanova-Smolenskaya, Miklina Ni, S. A. Klyushnikov, Svetlana A. Limborska, R. A. Rakhmonov
Publikováno v:
Russian Journal of Genetics. 38:1447-1451
Essential tremor (ET) is the most common extrapyramidal disorder of the central nervous system with autosomal dominant transmission in the majority of cases and age-dependent penetrance of the mutant gene. In a number of cases, it shares some phenoty
Autor:
Elena V. Filatova, Maria Shadrina, Irina A. Ivanova-Smolenskaya, Svetlana A. Limborska, E. Yu. Fedotova, Petr Slominsky, Sergey N. Illarioshkin
Publikováno v:
Molecular Genetics, Microbiology and Virology. 26:47-49
Parkinson’s disease (PD) is the second most common progressive neurodegenerative disease that arises as a result of the destruction of dopaminergic neurons. Reasons for the development of PD are not completely clarified and, at present, a number of
Autor:
Alexis Brice, Markova Ed, Sergei N. Illarioshkin, Rahmatullo A. Rahmonov, Irina A. Ivanova-Smolenskaya, Giovanni Stevanin
Publikováno v:
Movement Disorders. 15:1020-1023