Illarioshkin SN - Search Results

1

A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia.

Illarioshkin SN, Shadrina MI, Slominsky PA, Bespalova EV, Zagorovskaya TB, Bagyeva GKh, Markova ED, Limborska SA, Ivanova-Smolenskaya IA. Illarioshkin SN, et al. Eur J Neurol. 2007 Apr;14(4):413-7. doi: 10.1111/j.1468-1331.2007.01685.x. Eur J Neurol. 2007. PMID: 17388990

2

[Clinical polymorphism and genetic heterogeneity of hereditary spastic ataxia].

Dadali EL, Illarioshkin SN, Markova ED, Ivanova-Smolenskaia IA. Dadali EL, et al. Among authors: illarioshkin sn. Zh Nevropatol Psikhiatr Im S S Korsakova. 1992;92(4):10-3. Zh Nevropatol Psikhiatr Im S S Korsakova. 1992. PMID: 1333696 Review. Russian.

3

[Nosologic place of Pierre Marie's disease].

Markova ED, Insarova NG, Gurskaia NZ, Illarioshkin SN. Markova ED, et al. Among authors: illarioshkin sn. Zh Nevropatol Psikhiatr Im S S Korsakova. 1989;89(3):3-7. Zh Nevropatol Psikhiatr Im S S Korsakova. 1989. PMID: 2728744 Russian.

4

Trinucleotide repeat length and rate of progression of Huntington's disease.

Illarioshkin SN, Igarashi S, Onodera O, Markova ED, Nikolskaya NN, Tanaka H, Chabrashwili TZ, Insarova NG, Endo K, Ivanova-Smolenskaya IA, et al. Illarioshkin SN, et al. Ann Neurol. 1994 Oct;36(4):630-5. doi: 10.1002/ana.410360412. Ann Neurol. 1994. PMID: 7944295

5

[Analysis of trinucleotide repeat expansion as a new mechanism of mutation in Huntington's chorea: theoretical and applied aspects].

Illarioshkin SN, Ivanova-Smolenskaia IA, Markova ED, Nikol'skaia NN, Chabrashvili TZ, Insarova NG. Illarioshkin SN, et al. Genetika. 1996 Jan;32(1):103-9. Genetika. 1996. PMID: 8647411 Russian.

6

[A new mechanism of mutation in man: expansion of trinucleotide repeats].

Illarioshkin SN, Ivanova-Smolenskaia IA, Markova ED. Illarioshkin SN, et al. Genetika. 1995 Nov;31(11):1478-89. Genetika. 1995. PMID: 8666217 Review. Russian.

7

[The molecular genetic approach to the study of dominant spinocerebellar ataxias].

Illarioshkin SN, Ovchinnikov IV, Ivanova-Smolenskaia IA, Vereshchagin NV, Markova ED, Miklina NI, Kliushnikov SA. Illarioshkin SN, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 1996;96(1):37-41. Zh Nevrol Psikhiatr Im S S Korsakova. 1996. PMID: 8677716 Russian.

8

X-linked nonprogressive congenital cerebellar hypoplasia: clinical description and mapping to chromosome Xq.

Illarioshkin SN, Tanaka H, Markova ED, Nikolskaya NN, Ivanova-Smolenskaya IA, Tsuji S. Illarioshkin SN, et al. Ann Neurol. 1996 Jul;40(1):75-83. doi: 10.1002/ana.410400113. Ann Neurol. 1996. PMID: 8687195

9

[Molecular genetic analysis--a new stage in the study of hereditary diseases of the central nervous system].

Ivanova-Smolenskaia IA, Vereshchagin NV, Markova ED, Limborskaia SA, Illarioshkin SN, Ovchinnikov IV. Ivanova-Smolenskaia IA, et al. Among authors: illarioshkin sn. Vestn Ross Akad Med Nauk. 1996;(4):6-10. Vestn Ross Akad Med Nauk. 1996. PMID: 8754071 Review. Russian.

10

Spinocerebellar ataxia type 1 in Russia.

Illarioshkin SN, Slominsky PA, Ovchinnikov IV, Markova ED, Miklina NI, Klyushnikov SA, Shadrina M, Vereshchagin NV, Limborskaya SA, Ivanova-Smolenskaya IA. Illarioshkin SN, et al. J Neurol. 1996 Jul;243(7):506-10. doi: 10.1007/BF00886871. J Neurol. 1996. PMID: 8836939

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