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Human Molecular Genetics|June 9, 1998
De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystoniaC Klein, M F Brin, D de Leon, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|November 24, 2004
[Clinical and genetic analysis of juvenile parkinsonism in Russia]T B Zagorovskaia, S N Illarioshkin, P A Slominskiĭ, et al.
Klinicheskaia Laboratornaia Diagnostika|January 7, 1998
[Automated cytophotomorphometric tests of blood smears in general clinical studies and population screening]V S Medovyĭ, V A Balabutkin, N V Verdenskaia, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|December 21, 2006
[7-year experience in usage of mirapex in patients with different forms of primary parkinsonism]S N Illarioshkin, I A Ivanova-Smolenskaia, T B Zagorovskaia, et al.
Brain : a Journal of Neurology|December 1, 1996
Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophyS N Illarioshkin, I A Ivanova-Smolenskaya, H Tanaka, et al.
Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|September 11, 2015
[Identification of people at the latent stage of Parkinson's disease (the PARKINLAR study): first results and an optimization of the algorithm]E Yu Fedotova, A O Chechetkin, N Yu Abramycheva, et al.
Biomeditsinskaia Khimiia|September 26, 2024
Registration of activity of a single molecule of horseradish peroxidase using a detector based on a solid-state nanoporeYu D Ivanov, A N Ableev, A V Vinogradova, et al.
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