Illarioshkin SN - Search Results

1

miRNA expression is highly sensitive to a drug therapy in Parkinson's disease.

Alieva AKh, Filatova EV, Karabanov AV, Illarioshkin SN, Limborska SA, Shadrina MI, Slominsky PA. Alieva AKh, et al. Among authors: illarioshkin sn. Parkinsonism Relat Disord. 2015 Jan;21(1):72-4. doi: 10.1016/j.parkreldis.2014.10.018. Epub 2014 Oct 27. Parkinsonism Relat Disord. 2015. PMID: 25465742

2

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

3

Clinical and molecular analysis of a large family with three distinct phenotypes of progressive muscular dystrophy.

Illarioshkin SN, Ivanova-Smolenskaya IA, Tanaka H, Vereshchagin NV, Markova ED, Poleshchuk VV, Lozhnikova SM, Sukhorukov VS, Limborska SA, Slominsky PA, Bulayeva KB, Tsuji S. Illarioshkin SN, et al. Brain. 1996 Dec;119 ( Pt 6):1895-909. doi: 10.1093/brain/119.6.1895. Brain. 1996. PMID: 9009996

4

The GTP cyclohydrolase I gene in Russian families with dopa-responsive dystonia.

Illarioshkin SN, Markova ED, Slominsky PA, Miklina NI, Popova SN, Limborska SA, Tsuji S, Ivanova-Smolenskaya IA. Illarioshkin SN, et al. Arch Neurol. 1998 Jun;55(6):789-92. doi: 10.1001/archneur.55.6.789. Arch Neurol. 1998. PMID: 9626769

5

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 dystonia.

Markova ED, Slominsky PA, Illarioshkin SN, Miklina NI, Popova SN, Limborska SA, Ivanova-Smolenskaya IA. Markova ED, et al. Among authors: illarioshkin sn. Eur J Neurol. 1999 Sep;6(5):605-8. doi: 10.1046/j.1468-1331.1999.650605.x. Eur J Neurol. 1999. PMID: 10457396

6

A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia.

Slominsky PA, Markova ED, Shadrina MI, Illarioshkin SN, Miklina NI, Limborska SA, Ivanova-Smolenskaya IA. Slominsky PA, et al. Among authors: illarioshkin sn. Hum Mutat. 1999 Sep 19;14(3):269. doi: 10.1002/(SICI)1098-1004(1999)14:3<269::AID-HUMU12>3.0.CO;2-9. Hum Mutat. 1999. PMID: 10477437

7

[Molecular-genetic analysis of torsion dystonia in Russia].

Markova ED, Slominskiĭ PA, Illarioshkin SN, Miklina NI, Shadrina MI, Popova SN, Limborskaia SA, Ivanova-Smolenskaia IA. Markova ED, et al. Among authors: illarioshkin sn. Genetika. 2000 Jul;36(7):952-8. Genetika. 2000. PMID: 10994500 Russian.

8

[7-year experience in usage of mirapex in patients with different forms of primary parkinsonism].

Illarioshkin SN, Ivanova-Smolenskaia IA, Zagorovskaia TB, Karabanov AV, Poleshchuk VV, Markova ED, Karpova EA, Polevaia EV, Bagyeva GKh, Timerbaeva SL, Nurmanova ShA. Illarioshkin SN, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2006;106(11):26-32. Zh Nevrol Psikhiatr Im S S Korsakova. 2006. PMID: 17180757 Russian.

9

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

10

[A PARK8 form of Parkinson's disease: a mutational analysis of the LRRK2 gene in Russian population].

Shadrina MI, Illarioshkin SN, Bagyeva GKh, Bespalova EV, Zagorodskaia TB, Slominskiĭ PA, Markova ED, Kliushnikov SA, Limborskaia SA, Ivanova-Smolenskaia IA. Shadrina MI, et al. Among authors: illarioshkin sn. Zh Nevrol Psikhiatr Im S S Korsakova. 2007;107(3):46-50. Zh Nevrol Psikhiatr Im S S Korsakova. 2007. PMID: 18379513 Russian.

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