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Familial hemiplegic migraine type 1
- ... CACNA1A gene have been identified in people with familial hemiplegic migraine type 1 (FHM1). This condition is characterized by migraines with ...
- ... SCN1A gene have been identified in people with familial hemiplegic migraine type 3 (FHM3), a form of migraine headache that runs in families. Each of these mutations changes a single protein building block (amino acid) in the NaV1.1 channel, which alters the channel's structure. The ...
- ... Organization for Rare Disorders (NORD) ClinicalTrials.gov MIGRAINE, FAMILIAL HEMIPLEGIC, 1; FHM1 MIGRAINE, FAMILIAL HEMIPLEGIC, 2; FHM2 MIGRAINE, FAMILIAL HEMIPLEGIC, 3; ...
- ... ATP1A2 gene have been identified in people with familial hemiplegic migraine type 2 (FHM2). This condition is characterized by migraine ... ATPase alpha2-subunit ATP1A2 gene in patients with familial hemiplegic ... phenotypes. Clin Genet. 2008 Jan;73(1):37-43. doi: 10.1111/j.1399-0004. ...
- ... The genetic features of 24 patients affected by familial and sporadic hemiplegic migraine. Neurol Sci. 2011 May;32 Suppl 1:S141-2. doi: 10.1007/s10072-011-0517- ...
- ... head.People with migraine, particularly women who have migraine with aura, have an increased risk of a type of stroke that is caused by a lack ... usually include additional signs and symptoms. For example, familial hemiplegic ... common disorder worldwide, affecting 1 in 7 people. Chronic migraines affect about 1 ...
- ... is thought to affect the function of several types of ion channels. In addition, the PRRT2 ... hemiplegic migraine. This condition is characterized by migraine headaches with ...