Testing Genes Implicated in the Novel Case of Familial Hemiplegic Migraine-Reference-Cited by-同舟云学术

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Testing Genes Implicated in the Novel Case of Familial Hemiplegic Migraine

Published:2016-10-19 Issue:2 Volume:7 Page:265-268
ISSN:2191-1630
Container-title:BioNanoScience
language:en
Short-container-title:BioNanoSci.

Author:

Khaiboullina S. F.,Mendelevich E. G.,Martynova E. V.,Davidyuk Y. N.,Giniatullin R. A.,Rizvanov A. A.

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Bioengineering

Link

http://link.springer.com/article/10.1007/s12668-016-0314-x/fulltext.html

Reference20 articles.

1. van den Maagdenberg, A. M., et al. (2007). Migraine: gene mutations and functional consequences. Current Opinion in Neurology, 20(3), 299–305.

2. Russell, M. B., & Ducros, A. (2011). Sporadic and familial hemiplegic migraine: pathophysiological mechanisms, clinical characteristics, diagnosis, and management. Lancet Neurology, 10(5), 457–470.

3. Montagna, P. (2000). Molecular genetics of migraine headaches: a review. Cephalalgia, 20(1), 3–14.

4. Stam, A. H., et al. (2008). CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine. Clinical Genetics, 74(5), 481–485.

5. Vanmolkot, K. R., et al. (2003). Novel mutations in the Na+, K + −ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. Annals of Neurology, 54(3), 360–366.

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Melkersson–Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants?;Genes;2023-07-20

2. SCN1A Mutation—Beyond Dravet Syndrome: A Systematic Review and Narrative Synthesis;Frontiers in Neurology;2021-12-24

3. Mutations in the Voltage Dependent Calcium Channel CACNA1A (P/Q type alpha 1A subunit) Causing Neurological Disorders - An Overview;Neurology India;2021

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