Hereditary spastic paraplegias
Kutlubaeva, R. F., Kutlubaev, M. A., Magzhanov, R. V., Sayfullina, E. V., Khidiyatova, I. M.
Published in Nervno-myshechnye bolezni (05.01.2024)
Published in Nervno-myshechnye bolezni (05.01.2024)
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Gaucher disease type 2 (case report)
Shagieva, D. R., Magzhanov, R. V., Rakhmatullin, A. R., Sayfullina, E. V., Musin, R. G.
Published in Russkiĭ zhurnal detskoĭ nevrologii (28.09.2020)
Published in Russkiĭ zhurnal detskoĭ nevrologii (28.09.2020)
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Depression and Anxiety in Parkinson’s Disease
Akhmadeeva, G. N., Magzhanov, R. V., Tayupova, G. N., Baitimerov, A. R., Khidiyatova, I. M.
Published in Neuroscience and behavioral physiology (01.06.2018)
Published in Neuroscience and behavioral physiology (01.06.2018)
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Clinical and epidemiological characteristics of hereditary motor-sensory neuropathy 1X caused by the mutation c. 259C> G (p. P87A) in the GJB1 gene of patients from the Republic of Bashkortostan
Saifullina, E V, Magzhanov, R V, Khidiyatova, I M, Khusnutdinova, E K
Published in Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova (2017)
Published in Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova (2017)
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Polymorphism of the apolipoprotein E gene and risk of multiple sclerosis in ethnic Russians
Mustafina, O. E, Mikhailova, A. M, Bakhtiyarova, K. Z, Nasibulin, T. R, Tuktarova, I. A, Makarycheva, O. Yu, Sudomoina, M. A, Boiko, A. N, Voronchikhina, S. A, Volkova, L. I, Magzhanov, R. V, Favorova, O. O
Published in Molecular biology (New York) (01.12.2008)
Published in Molecular biology (New York) (01.12.2008)
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Analysis of hormone-dependent pathology in female patients with juvenile myoclonic epilepsy
Anisimova, D. V., Magzhanov, R. V., Vlasov, P. N., Petrukhin, V. A., Tsevtsivadze, E. B., Nurmukhametova, S. R.
Published in Nevrologii͡a︡, neĭropsikhiatrii͡a︡, psikhosomatika (01.06.2017)
Published in Nevrologii͡a︡, neĭropsikhiatrii͡a︡, psikhosomatika (01.06.2017)
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The pattern of female genital hormonal disease in juvenile myoclonic epilepsy
Anisimova, D. V., Magzhanov, R. V., Vlasov, P. N., Petrukhin, V. A., Tsevtsevadze, E. B., Nurmukhametova, S. R., Garifullina, F. Yu
Published in Nevrologii͡a︡, neĭropsikhiatrii͡a︡, psikhosomatika (01.07.2016)
Published in Nevrologii͡a︡, neĭropsikhiatrii͡a︡, psikhosomatika (01.07.2016)
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MFN2 gene analysis in patients with hereditary motor and sensory neuropathy from Bashkortostan Republic
Khidiyatova, I. M., Skachkova, I. A., Saifullina, E. V., Magzhanov, R. V., Schagina, O. A., Zinchenko, R. A., Petrin, A. N., Khusnutdinova, E. K.
Published in Russian journal of genetics (01.07.2013)
Published in Russian journal of genetics (01.07.2013)
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Glutaric aciduria type 1 in children. Clinical presentation of 46 cases in Russian families
Mikhailova, S V, Saifullina, E V, Baranova, P V, Vorontsova, V P, Gribov, D I, Zhivihina, M V, Slatetskaya, A N, Magzhanov, R V, Samokhvalov, V A, Virtseva, M N, Borscheva, L P, Koh, E E, Novikova, M V, Abrukova, A V, E. Yu. Belyashova, N. Yu. Gerasimenko, Guseva, L V, Yukhimenko, Zh V, Nikitina, N V, Belyaeva, T I, Shkurko, T A, Pichkur, N A, Kakaulina, V S, Pechatnikova, N L, N . A. Polyakova, Korostelev, S A, Pyankov, D V, Kanivets, I V, Demina, N A, E. Yu. Pyrkova, Baidakova, G V, Kurkina, M V, E. Yu. Zakharova
Published in Nervno-myshechnye bolezni (01.01.2021)
Published in Nervno-myshechnye bolezni (01.01.2021)
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