Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Varvara A. Kadnikova"'
Autor:
Galina E. Rudenskaya, Varvara A. Kadnikova, Oksana P. Ryzhkova, Nina A. Dyomina, Inna V. Sharkova, Alexander V. Polyakov
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 15, Iss 2, Pp 13-20 (2021)
Introduction. Since 2017, the Research Centre for Medical Genetics has been conducting the first clinical and molecular study in Russia of a heterogeneous spastic paraplegia group based on the MPS high throughput sequencing method. Our group of molec
Externí odkaz:
https://doaj.org/article/a61d816dee3049b39be805c39aa7b9f7
Autor:
Galina E. Rudenskaya, Varvara A. Kadnikova, Oksana P. Ryzhkova, Inga V. Anisimova, Elena L. Dadaly, Nina A. Dyomina, Irina A. Mishina, Ilya V. Kanivets, Anna V. Antonetz, Alexander V. Polyakov
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 14, Iss 4, Pp 29-38 (2020)
Introduction. A heterogeneous group of hereditary spastic paraplegias (HSP) with known causative genes, alongside the predominant autosomal dominant ones, includes numerous and diagnostically more complex autosomal recessive (AR) forms with diverse p
Externí odkaz:
https://doaj.org/article/4140eebb4fc04a26a5c3f2372b904175
Autor:
Galina E. Rudenskaya, Varvara A. Kadnikova, Christian Beetz, Tatyana N. Proskokova, Irina G. Sermyagina, Anna A. Stepanova, Valery P. Fedotov, Elena L. Dadaly, Darya M. Guseva, Тatiana V. Markova, Oksana P. Ryzhkova
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 14, Iss 1, Pp 44-54 (2020)
Introduction. The autosomal dominant hereditary spastic paraplegia type 3 (SPG3), associated with the ATL1 gene, is a common form of the hereditary spastic paraplegia (HSP). The molecular genetic and clinical features of the SPG3 have not been suffic
Externí odkaz:
https://doaj.org/article/cb785b6c298746ea89b96a7bb419e2f1