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Molekuliarnaia Genetika, Mikrobiologiia I Virusologiia|July 27, 2011
[Analysis of single nucleotide polymorphism rs415430 in the WNT3 gene in the Russian population with the Parkinson disease]E V Filatova, M I Shadrina, E Iu Fedotova, et al.Voprosy Meditsinskoi Khimii|January 1, 1997
[Immunochemical correlates of the severity of Parkinson's disease]S G Morozov, I A Ivanova-Smolenskaia, E D Markova, et al.Human Mutation|September 8, 1999
A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystoniaP A Slominsky, E D Markova, M I Shadrina, et al.European Journal of Neurology|August 24, 1999
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 dystoniaE D Markova, P A Slominsky, S N Illarioshkin, et al.Neurology|January 3, 2001
Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathyS N Illarioshkin, I A Ivanova-Smolenskaya, C R Greenberg, et al.Journal of Neurology|February 1, 2000
Studies of the candidate genes in X-linked congenital cerebellar hypoplasiaS N Illarioshkin, K M Allen, J G Gleeson, et al.Genetika|February 28, 1998
[Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13]S N Illarioshkin, I A Ivanova-Smolenskaia, S A Dimborskaia, et al.Kardiologiia|September 2, 2004
[Anticholinergic Effect of a New Antiarrhythmic Class III Drug RG-2]V V Fedorov, I A Ivanova, A V Glukhov, et al.Zhurnal Nevropatologii I Psikhiatrii Imeni S.S. Korsakova (Moscow, Russia : 1952)|January 1, 1990
[Clinico-immunologic correlations and various characteristics of the lymphocyte receptors in hepatocerebral dystrophy]I V Gannushkina, I G Zhirnova, A Chlonkovska, et al.Vestnik Rossiiskoi Akademii Meditsinskikh Nauk|May 1, 1999
[Adamantane derivatives enhancing body's resistance to emergencies]I S Morozov, N V Klimova, S A Sergeeva, et al.Pageof 15