Limborska SA - 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: limborska sa. 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

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

3

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

4

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

5

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

6

Apolipoprotein B 3'-VNTR polymorphism in the Udmurt population.

Spitsyn VA, Khorte MV, Pogoda TV, Slominsky PA, Nurbaev SD, Agapova RK, Limborska SA. Spitsyn VA, et al. Among authors: limborska sa. Hum Hered. 2000 Jul-Aug;50(4):224-6. doi: 10.1159/000022919. Hum Hered. 2000. PMID: 10782013

7

CuZn-superoxide dismutase gene in sporadic amyotrophic lateral sclerosis patients from Russia: Asp90Ala (D90A) mutation and novel rare polymorphism IVS3+35 A>C.

Slominsky PA, Shadrina MI, Kondratyeva EA, Tupitsina TV, Levitsky GN, Skvortsova VI, Limborska SA. Slominsky PA, et al. Among authors: limborska sa. Hum Mutat. 2000 Sep;16(3):277-8. doi: 10.1002/1098-1004(200009)16:3<277::AID-HUMU27>3.0.CO;2-P. Hum Mutat. 2000. PMID: 10980551 No abstract available.

8

Sporadic ALS associated with the D90A Cu,Zn superoxide dismutase mutation in Russia.

Skvortsova VI, Limborska SA, Slominsky PA, Levitskaya NI, Levitsky GN, Shadrina MI, Kondratyeva EA. Skvortsova VI, et al. Among authors: limborska sa. Eur J Neurol. 2001 Mar;8(2):167-72. doi: 10.1046/j.1468-1331.2001.00186.x. Eur J Neurol. 2001. PMID: 11284995 Review.

9

Rapid induction of neurotrophin mRNAs in rat glial cell cultures by Semax, an adrenocorticotropic hormone analog.

Shadrina MI, Dolotov OV, Grivennikov IA, Slominsky PA, Andreeva LA, Inozemtseva LS, Limborska SA, Myasoedov NF. Shadrina MI, et al. Among authors: limborska sa. Neurosci Lett. 2001 Aug 3;308(2):115-8. doi: 10.1016/s0304-3940(01)01994-2. Neurosci Lett. 2001. PMID: 11457573

10

Polymorphism of trinucleotide repeats in loci DM, DRPLA and SCA1 in East European populations.

Popova SN, Slominsky PA, Pocheshnova EA, Balanovskaya EV, Tarskaya LA, Bebyakova NA, Bets LV, Ivanov VP, Livshits LA, Khusnutdinova EK, Spitcyn VA, Limborska SA. Popova SN, et al. Among authors: limborska sa. Eur J Hum Genet. 2001 Nov;9(11):829-35. doi: 10.1038/sj.ejhg.5200716. Eur J Hum Genet. 2001. PMID: 11781699

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