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Familial hemiplegic migraine
- ... ATP1A2 gene have been identified in people with familial hemiplegic migraine type 2 (FHM2). This condition is characterized by ... are not as well-studied as those in familial hemiplegic migraine, it is thought that they have similar effects: ...
- ... PRRT2 gene have been identified in people with familial hemiplegic migraine. This condition is characterized by migraine headaches with ... pattern of neurological symptoms known as aura. In familial hemiplegic migraine, the aura includes temporary numbness or weakness on ...
- ... CACNA1A gene have been identified in people with familial hemiplegic migraine type 1 (FHM1). This condition is characterized by ... a dozen families. The CACNA1A variants that cause familial hemiplegic migraine are called gain-of-function variants, because they ...
- ... SCN1A gene have been identified in people with familial hemiplegic migraine type 3 (FHM3), a form of migraine headache ... the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. Lancet. 2005 Jul 30-Aug 5;366(9483): ...