E. Markova

Most-cited papers

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

   S. Illarioshkin, I. Ivanova-Smolenskaya, C. R. Greenberg, E. Nylen +4 more

   2000Neurology128 citations

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

   S. Illarioshkin, S. Igarashi, O. Onodera, E. Markova +7 more

   1994Annals of Neurology103 citations

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3. Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism

   S. Illarioshkin, M. Periquet, N. Rawal, C. Lücking +7 more

   2003Movement Disorders33 citations

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

   S. Illarioshkin, E. Markova, P. A. Slominsky, N. Miklina +4 more

   1998Archives of Neurology29 citations Open access

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5. Spinocerebellar ataxia type 1 in Russia

   S. Illarioshkin, P. A. Slominsky, I. Ovchinnikov, E. Markova +6 more

   1996Journal of Neurology27 citations

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

   S. Illarioshkin, G. K. Bagieva, S. Klyushnikov, I. Ovchinnikov +2 more

   2000European Journal of Neurology14 citations

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7. Lack of α-synuclein gene mutations in families with autosomal dominant Parkinson's disease in Russia

   S. Illarioshkin, I. Ivanova-Smolenskaya, E. Markova, T. Zagorovskaya +1 more

   2000Journal of Neurology9 citations

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8. Peculiarities of Carnosine Metabolism in a Patient with Pronounced Homocarnosinemia

   G. Kramarenko, E. Markova, I. Ivanova-Smolenskaya, Alexander A. Boldyrev

   2001Bulletin of experimental biology and medicine8 citations

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

   S. N. Illarioshkin, I. Ivanova-smolenskaia, E. Markova, N. N. Nikol'skaia +2 more

   1996Genetika7 citations

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10. [Clinical and genetic analysis of juvenile parkinsonism in Russia].

    T. B. Zagorovskaia, S. N. Illarioshkin, P. A. Slominskii, I. Ivanova-smolenskaia +7 more

    2004Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova4 citations

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11. [Immunochemical correlates of the severity of Parkinson's disease].

    S. Morozov, I. Ivanova-smolenskaia, E. Markova, M. Piradov +3 more

    1997Voprosy medicinskoj himii4 citations

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

    S. N. Illarioshkin, I. Ivanova-smolenskaia, E. Markova

    1995Genetika4 citations

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

    M. Shadrina, S. Illarioshkin, G. Bagyeva, E. Bespalova +6 more

    2007Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova3 citations

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

    S. Illarioshkin, K. Allen, J. Gleeson, S. Tsuji +4 more

    1999Journal of Neurology3 citations

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15. [The surgical results in patients with different forms of torsion dystonia].

    E. Sungurov, V. Peresedov, E. Markova, I. Ivanova-smolenskaia +2 more

    1998Voprosy neirokhirurgii imeni N N Burdenko3 citations

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16. Novel mutational mechanism in man: Expansion of trinucleotide repeats

    S. N. Ilarioshkin, I. Ivanova-Smolenskaya, E. Markova

    19953 citations

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17. [Comparative study of human erythrocyte membranes in normal people and in Huntington's chorea patients].

    S. F. Zakharov, A. M. Shandala, M. V. Shcheglova, P. Gromov +5 more

    1990Voprosy medicinskoj himii3 citations

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18. 2.206 Carnosine increases efficiency of L-DOPA therapy of parkinsonics

    A. Boldyrev, N. Fedorova, S. Stvolinsky, M. Stepanova +6 more

    20072 citations

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19. [7-year experience in usage of mirapex in patients with different forms of primary parkinsonism].

    S. N. Illarioshkin, I. Ivanova-smolenskaia, T. B. Zagorovskaia, A. Karabanov +7 more

    2006Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova2 citations

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

    E. Markova, P. A. Slominskii, S. N. Illarioshkin, N. Miklina +4 more

    2000Genetika2 citations

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21. [Mapping of the gene for autosomal-recessive progressive muscular dystrophy in an isolate from a highland region of Dagestan to chromosome 2-13].

    S. N. Illarioshkin, I. Ivanova-smolenskaia, S. A. Dimborskaia, V. Poleshchuk +4 more

    1997Genetika2 citations

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22. 5-29-06 Molecular analysis in Russian families with Wilson's disease

    I. Ivanova-Smolenskaya, A. Karabanov, Sergey N. Illarioshkin, I. Ovchinnikov +2 more

    19972 citations

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23. Programmed type movement in patients with lesion to different cerebellar systems

    N. Burlachkova, N. Gurskaya, I. Kozlovskaya, E. Markova

    1986Neurophysiology (New York)2 citations

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24. [Quantitative evaluation of the T- and B-systems of immunity in various hereditary diseases of the nervous system].

    I. Gannushkina, I. Zhirnova, N. Г. Toropova, T. D. Toporkina +1 more

    1981Zhurnal Nevropatologii I Psikhiatrii Imeni S S Korsakova2 citations

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25. [Nervous tissue protein autoantibodies in hepatolenticular degeneration].

    S. Morozov, M. P. Usanova, V. Poleshchuk, A. V. Poletaev +2 more

    2001Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova1 citations

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26. [Molecular genetics of the hereditary dystonic syndromes].

    S. N. Illarioshkin, E. Markova, N. Miklina, I. A. Ivanova-Smolianskaia

    2000Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova1 citations

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27. [Friedreich's disease: a real spectrum of clinical manifestations in terms of direct DNA diagnosis].

    S. N. Illarioshkin, E. B. Drizuna, G. K. Bagieva, E. Markova +3 more

    1999Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova1 citations

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28. [Molecular genetic testing in the diagnosis of sporadic cases of Huntington's chorea].

    I. Ivanova-smolenskaia, I. Ovchinnikov, S. N. Illarioshkin, E. Markova +3 more

    1998Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova1 citations

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29. [Presymptomatic DNA diagnosis of spinocerebellar ataxia type 1].

    S. N. Illarioshkin, I. Ivanova-smolenskaia, S. A. Limborskaia, I. Ovchinnikov +4 more

    1997Genetika1 citations

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30. [A new form of hereditary ataxia: X-linked congenital cerebellar hypoplasia (a clinical and molecular genetic analysis)].

    S. N. Illarioshkin, I. Ivanova-smolenskaia, E. Markova, N. N. Nikol'skaia +1 more

    1997Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova1 citations

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

    S. N. Illarioshkin, I. Ovchinnikov, I. Ivanova-smolenskaia, N. Vereshchagin +3 more

    1996Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova1 citations

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32. [Pathological status of catecholamines in the corpus striatum in hepatocerebral dystrophy (Wilson-Konovalov disease)].

    V. P. Barkhatova, E. G. Larskiĭ, I. Ivanova-smolenskaia, E. Markova +1 more

    1992Zhurnal Nevropatologii I Psikhiatrii Imeni S S Korsakova1 citations

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33. [Ceruloplasmin activity in the blood during progressive diseases of the central nervous system].

    T. I. Mzhel'skaia, I. Zavalishin, I. Ivanova-smolenskaia, E. G. Larskiĭ +3 more

    1989Laboratornoe delo1 citations

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34. [Pathogenesis and treatment of torsion dystonia].

    V. P. Barkhatova, E. Markova

    1978Zhurnal Nevropatologii I Psikhiatrii Imeni S S Korsakova1 citations

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35. Nikolai V. Konovalov (1900–1966): His Role in the Development of Neurology and the Creation of the Institute of Neurology of the Russian Academy of Medical Sciences

    I. Ivanova-Smolenskaya, E. Markova

    2007Journal of the History of the Neurosciences0 citations

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36. Impaired step-tracking control in patients with cerebellar and pyramidal lesions

    N. Burlachkova, N. Gurskaya, I. Kozlovskaya, E. Markova

    2005Neurophysiology (New York)0 citations

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37. [Voluntary postural control learning with a use of visual bio-feedback in patients with spinocerebellar degenerations].

    Ksenia I. Ustinova, M. Ioffe, L. Chernikova, M. Kulikov +2 more

    2004Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova0 citations

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38. [Cytochemical activity of mitochondrial enzymes in Parkinson's disease].

    E. V. Polevaia, I. Ivanova-smolenskaia, S. N. Illarioshkin, V. Sukhorukov +1 more

    2004Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova0 citations

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39. [Clinical and stabilometric analysis of postural instability in Parkinson's disease].

    E. Karpova, I. Ivanova-smolenskaia, L. A. Chernikova, E. Markova +1 more

    2004Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova0 citations

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40. [Regularities of fixation of brain serum antibodies from patients with lateral amyotrophic sclerosis in rabbit CNS].

    L. S. Musaeva, I. V. Gannyshkina, I. Zavalishin, E. Markova +1 more

    2002Patologicheskaia fiziologiia i eksperimental'naia terapiia0 citations

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41. [Analysis of mutations in ATP7B gene and experience with direct DNA-diagnosis in hepato-lenticular degeneration].

    A. Karabanov, I. Ovchinnikov, S. N. Illarioshkin, V. Poleshchuk +5 more

    2001Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova0 citations

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42. [Botulin A toxin: a highly effective drug in the treatment of focal dystonia].

    S. Timerbaeva, I. Ivanova-smolenskaia, E. Markova, V. Poleshchuk +2 more

    2000Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova0 citations

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43. [Acoustic brain stem and cognitive evoked potentials (P300) in patients with hepatolenticular degeneration].

    V. V. Gnezditskiĭ, P. Fedin, V. Poleshchuk, E. Markova +1 more

    2000Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova0 citations

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44. Long-term results of stereotactic operations in patients with torsion dystonia

    E. Sungurov, E. Markova, V. Peresdov, V. Tjiumikov +1 more

    19970 citations

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

    I. Ivanova-smolenskaia, N. Vereshchagin, E. Markova, S. A. Limborskaia +2 more

    1996Vestnik Rossiiskoi akademii meditsinskikh nauk0 citations

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46. [Search for expansion of CAG-repeats in DNA sequences expressed in the brain of humans with psychiatric and neurological diseases].

    I. Ovchinnikov, E. Braga, M. Aksenova, E. Druzina +5 more

    1996Voprosy medicinskoj himii0 citations

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47. [Genetic study of idiopathic torsion dystonia in Russia].

    E. Dadali, E. Markova, A. N. Petrin, I. Ivanova-smolenskaia +1 more

    1996Genetika0 citations

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48. [Triplet expansion analysis--a new molecular genetic method for studying the mechanism of mutations in neurogenetics (exemplified by Huntington chorea)].

    I. Ivanova-smolenskaia, N. Vereshchagin, S. N. Illarioshkin, E. Markova +3 more

    1995Zhurnal Nevrologii i Psikhiatrii imeni S.S. Korsakova0 citations

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49. [Molecular-genetic analysis of Huntington chorea (review of the foreign literature)].

    I. Ivanova-smolenskaia, T. I. Mzhel'skaia, Iu K Milovidov, T. S. Gulevskaia +1 more

    1992Zhurnal Nevropatologii I Psikhiatrii Imeni S S Korsakova0 citations

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50. Parkinsonian hereditary syndromes and their phenotypes

    I. Ivanova-Smolenskaya, E. Markova

    19920 citations

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