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HEMIPLEGIC MIGRAINE

https://doi.org/10.1234/XXXX-XXXX-2013-4-3-7

Abstract

Familial hemiplegic migraine is only one type of migraine with well-studied molecular genetic mechanism. This is a rare neurological disease of humans that is described only in 200 families worldwide and in sporadic forms. However, understanding of the molecular mechanisms of hemiplegic migraine expands our understanding of the etiology of classical migraine. In this review available to date information about the genetic basis of hemiplegic migraine, its clinical presentations and a brief overview of approaches to treatment are presented.

 

About the Authors

J. E. Azimova
Laboratory of Neurology and Clinical Neurophysiology, Department of Neuroscience, Scientific-Research Centre, I.M. Sechenov First Moscow State Medi cal University, Moscow; University headache clinic, Moscow
Russian Federation

 

 



Е. А. Klimov
Bioiogical faculty of Lomonosov Moscow State University, Moscow
Russian Federation


K. V. Skorobogatykh
Laboratory of Neurology and Clinical Neurophysiology, Department of Neuroscience, Scientific-Research Centre, I.M. Sechenov First Moscow State Medi cal University, Moscow; University headache clinic, Moscow
Russian Federation


А. V. Sergeev
Laboratory of Neurology and Clinical Neurophysiology, Department of Neuroscience, Scientific-Research Centre, I.M. Sechenov First Moscow State Medi cal University, Moscow; University headache clinic, Moscow
Russian Federation


Z. G. Kokaeva
Bioiogical faculty of Lomonosov Moscow State University, Moscow
Russian Federation


G. R. Tabeeva
Laboratory of Neurology and Clinical Neurophysiology, Department of Neuroscience, Scientific-Research Centre, I.M. Sechenov First Moscow State Medi cal University, Moscow; University headache clinic, Moscow
Russian Federation


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Review

For citations:


Azimova J.E., Klimov Е.А., Skorobogatykh K.V., Sergeev А.V., Kokaeva Z.G., Tabeeva G.R. HEMIPLEGIC MIGRAINE. Medical Genetics. 2013;12(4):3-7. (In Russ.) https://doi.org/10.1234/XXXX-XXXX-2013-4-3-7

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