Migraine: gene mutations and functional consequences-Reference-Cited by-同舟云学术

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Migraine: gene mutations and functional consequences

Published:2007-06 Issue:3 Volume:20 Page:299-305
ISSN:1350-7540
Container-title:Current Opinion in Neurology
language:en
Short-container-title:Current Opinion in Neurology

Author:

van den Maagdenberg Arn MJM,Haan Joost,Terwindt Gisela M,Ferrari Michel D

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Neurology

Reference67 articles.

1. Recent advances in understanding migraine mechanisms, molecules and therapeutics

2. Increased risk of migraine with typical aura in probands with familial hemiplegic migraine and their relatives

3. Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

Cited by 115 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. Unravelling the Genetic Landscape of Hemiplegic Migraine: Exploring Innovative Strategies and Emerging Approaches;Genes;2024-03-31

2. Glutamate in Migraine Neurobiology and Treatment;Glutamate and Neuropsychiatric Disorders;2022

3. Migraine;Neuroscience in the 21st Century;2022

4. Rolling Nagoya Mouse;Handbook of the Cerebellum and Cerebellar Disorders;2021-12-05

5. UNC-2 CaV2 Channel Localization at Presynaptic Active Zones Depends on UNC-10/RIM and SYD-2/Liprin-α in Caenorhabditis elegans;The Journal of Neuroscience;2021-05-11

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