Familial Hemiplegic Migraine
What's New
Last Posted: Jan 16, 2025
- Exploring the association between familial hemiplegic migraine genes (CACNA1A, ATP1A2 and SCN1A) with migraine and epilepsy: A UK Biobank exome-wide association study.
Christian Staehr, et al. Cephalalgia : an international journal of headache 2025 0 (1) 3331024241306103 - De novo SCN1A missense variant in a patient with Parkinson's disease.
Majed Alluqmani, et al. Frontiers in genetics 2024 0 1496683 - Efficacy of galcanezumab in proline-rich transmembrane protein 2 (PRRT2)-associated familial hemiplegic migraine: A case series.
Costanza Sottani, et al. Headache 2024 0 - Familial hemiplegic migraine in pediatric patients: A genetic, clinical, and follow-up study.
Giuseppe Donato Mangano, et al. Headache 2023 0 - Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study.
Riant Florence, et al. Neurology 2021 0 (1) e51-e61 - Epilepsy in patients with familial hemiplegic migraine.
Has?rc? Bay?r Buse Rahime, et al. Seizure 2021 0 87-94 - Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine.
Rasmussen Andreas Hoiberg, et al. Journal of medical genetics 2020 0 (9) 610-616 - [An update on the familial headache syndromes].
Takeshima Takao, et al. Rinsho shinkeigaku = Clinical neurology 2005 0 (11) 944-7 - Possible Involvement of the CACNA1E Gene in Migraine: A Search for Single Nucleotide Polymorphism in Different Clinical Phenotypes.
Ambrosini Anna, et al. Headache 2017 6 - Molecular factors in migraine.
Kowalska Marta, et al. Oncotarget 2016 5
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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