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familial type 2 Hemiplegic migraine

An autosomal dominant type of familial hemiplegic migraine (Migraine with Aura) with onset between 6 to 30 years and characterized by hemiparesis or paresthesias, aphasia, headaches, and behavioral changes, with subsequent loss of consciousness. Mutations in the ATP1A2 gene have been identified. OMIM: 602481
Also Known As:
Hemiplegic migraine, familial type 2; Familial hemiplegic migraine, type 2; Migraine, familial hemiplegic, 2
Networked: 36 relevant articles (0 outcomes, 1 trials/studies)

Disease Context: Research Results

Related Diseases

1. Migraine with Aura (Familial Hemiplegic Migraine)
2. Dystonia 12
3. Migraine Disorders (Migraine)
4. Alternating hemiplegia of childhood
5. Nervous System Diseases (Neurological Disorders)

Experts

1. Lykke-Hartmann, Karin: 6 articles (01/2022 - 02/2012)
2. Pietrobon, Daniela: 4 articles (01/2021 - 06/2011)
3. Aalkjaer, Christian: 2 articles (01/2022 - 01/2019)
4. Staehr, Christian: 2 articles (01/2022 - 01/2019)
5. Conti, Fiorenzo: 2 articles (01/2021 - 01/2016)
6. Melone, Marcello: 2 articles (01/2021 - 01/2016)
7. Kawakami, Kiyoshi: 2 articles (01/2020 - 01/2018)
8. Santello, Mirko: 2 articles (01/2020 - 01/2016)
9. Friedrich, Thomas: 2 articles (11/2017 - 11/2008)
10. Tavraz, Neslihan N: 2 articles (11/2017 - 11/2008)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to familial type 2 Hemiplegic migraine:
1. SodiumIBA
2. PotassiumIBA
3. Adenosine Triphosphatases (ATPase)IBA
4. Protein Isoforms (Isoforms)IBA
5. Glutamic Acid (Glutamate)FDA Link
6. Sodium-Potassium-Exchanging ATPase (Sodium, Potassium ATPase)IBA
7. Potassium Channels (Potassium Channel)IBA
8. Protons (Proton)IBA
9. Proteins (Proteins, Gene)FDA Link
10. Nitric Oxide (Nitrogen Monoxide)FDA Link