Markova ED - 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: markova ed. 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

Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology.

Shadrina M, Nikopensius T, Slominsky P, Illarioshkin S, Bagyeva G, Markova E, Ivanova-Smolenskaia I, Kurg A, Limborska S, Metspalu A. Shadrina M, et al. Neurosci Lett. 2006 Sep 25;405(3):212-6. doi: 10.1016/j.neulet.2006.06.066. Epub 2006 Jul 28. Neurosci Lett. 2006. PMID: 16876316

3

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. Among authors: markova ed. J Neurol. 1996 Jul;243(7):506-10. doi: 10.1007/BF00886871. J Neurol. 1996. PMID: 8836939

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. Among authors: markova ed. 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. 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

Studies of the candidate genes in X-linked congenital cerebellar hypoplasia.

Illarioshkin SN, Allen KM, Gleeson JG, Tsuji S, Ikeuchi T, Markova ED, Walsh CA, Ivanova-Smolenskaya IA. Illarioshkin SN, et al. Among authors: markova ed. J Neurol. 1999 Dec;246(12):1177-80. doi: 10.1007/s004150050539. J Neurol. 1999. PMID: 10653312

7

Different phenotypes of Friedreich's ataxia within one 'pseudo-dominant' genealogy: relationships between trinucleotide (GAA) repeat lengths and clinical features.

Illarioshkin SN, Bagieva GK, Klyushnikov SA, Ovchinnikov IV, Markova ED, Ivanova-Smolenskaya IA. Illarioshkin SN, et al. Among authors: markova ed. Eur J Neurol. 2000 Sep;7(5):535-40. doi: 10.1046/j.1468-1331.2000.t01-1-00113.x. Eur J Neurol. 2000. PMID: 11054139

8

Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy.

Illarioshkin SN, Ivanova-Smolenskaya IA, Greenberg CR, Nylen E, Sukhorukov VS, Poleshchuk VV, Markova ED, Wrogemann K. Illarioshkin SN, et al. Among authors: markova ed. Neurology. 2000 Dec 26;55(12):1931-3. doi: 10.1212/wnl.55.12.1931. Neurology. 2000. PMID: 11134403

9

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. Among authors: markova ed. Ann Neurol. 1994 Oct;36(4):630-5. doi: 10.1002/ana.410360412. Ann Neurol. 1994. PMID: 7944295

10

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: markova ed. Brain. 1996 Dec;119 ( Pt 6):1895-909. doi: 10.1093/brain/119.6.1895. Brain. 1996. PMID: 9009996

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