Limborska SA - 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. Among authors: limborska sa. 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

Special Issue "Genomics of Stroke" 2022.

Limborska SA, Filippenkov IB. Limborska SA, et al. Genes (Basel). 2023 Feb 17;14(2):514. doi: 10.3390/genes14020514. Genes (Basel). 2023. PMID: 36833441 Free PMC article.

3

Neuroprotective Peptides and New Strategies for Ischemic Stroke Drug Discoveries.

Dergunova LV, Filippenkov IB, Limborska SA, Myasoedov NF. Dergunova LV, et al. Among authors: limborska sa. Genes (Basel). 2023 Apr 22;14(5):953. doi: 10.3390/genes14050953. Genes (Basel). 2023. PMID: 37239313 Free PMC article. Review.

4

Heterogeneity of beta-thalassemia in Azerbaidzhan.

Dergunova LV, Ryskov AP, Slominsky PA, Rustamov RS, Limborska SA. Dergunova LV, et al. Among authors: limborska sa. Haematologia (Budap). 1984;17(4):473-81. Haematologia (Budap). 1984. PMID: 6241915

5

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. Among authors: limborska sa. Brain. 1996 Dec;119 ( Pt 6):1895-909. doi: 10.1093/brain/119.6.1895. Brain. 1996. PMID: 9009996

6

Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium.

Ozelius LJ, Hewett J, Kramer P, Bressman SB, Shalish C, de Leon D, Rutter M, Risch N, Brin MF, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, McCormick MK, Fahn S, Buckler AJ, Gusella JF, Breakefield XO. Ozelius LJ, et al. Among authors: limborska sa. Genome Res. 1997 May;7(5):483-94. doi: 10.1101/gr.7.5.483. Genome Res. 1997. PMID: 9149944 Free article.

7

De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.

Klein C, Brin MF, de Leon D, Limborska SA, Ivanova-Smolenskaya IA, Bressman SB, Friedman A, Markova ED, Risch NJ, Breakefield XO, Ozelius LJ. Klein C, et al. Among authors: limborska sa. Hum Mol Genet. 1998 Jul;7(7):1133-6. doi: 10.1093/hmg/7.7.1133. Hum Mol Genet. 1998. PMID: 9618171

8

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. Among authors: limborska sa. Arch Neurol. 1998 Jun;55(6):789-92. doi: 10.1001/archneur.55.6.789. Arch Neurol. 1998. PMID: 9626769

9

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: limborska sa. Eur J Neurol. 1999 Sep;6(5):605-8. doi: 10.1046/j.1468-1331.1999.650605.x. Eur J Neurol. 1999. PMID: 10457396

10

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: limborska sa. 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

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