.... Abstract Familial hemiplegic migraine type 2 results from pathogenic variants in the ATP1A2 gene, which encodes for a catalytic subunit of sodium/potassium ATPase. This extremely rare autosomal dominant disorder manifests with a spectrum of symptoms, most commonly pure hemiplegic phenotype...

...Lokesh Saini; Pradeep Kumar Gunasekaran; Sarbesh Tiwari; Bharat Choudhary; Sujatha Manjunathan; Ashna Kumar Familial hemiplegic migraine (FHM), an autosomal dominant subtype of hemiplegic migraine, is a channelopathy presenting with severe headache, visual field defects, nystagmus, paresthesia...

.... Clinically, the two are often treated in a similar manner ^{7 , 9 – 11} however, instances of more severe phenotypes (i.e., hemiplegic migraine) may present unique challenges both for military providers as well as force readiness. Abstract Introduction Headaches are one of the world’s most common...

... of neuronal hyperexcitability, rather than a PRRT2 specific molecular mechanism. However, it remains to be established whether novel PRRT2-associated diseases, such as for example hemiplegic migraine attacks, respond to classic anticonvulsants in the same way that classic PKD attacks do...

... 22 4 2010 31 8 2010 11 9 2010 © The Author (2010). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved. For Permissions, please email: [email protected] 2010 Abstract Episodic ataxia type 2 and familial hemiplegic migraine...

...L. L. Thomsen; M. Kirchmann; A. Bjornsson; H. Stefansson; R. M. Jensen; A. C. Fasquel; H. Petursson; M. Stefansson; M. L. Frigge; A. Kong; J. Gulcher; K. Stefansson; J. Olesen Abstract Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura and transient hemiplegia. FHM...

... of Copenhagen, Department of Neurology, Glostrup Hospital, Ndr. Ringvej 57, 2600 Glostrup, Denmark E‐mail: [email protected] 24 01 2002 25 10 2001 16 01 2002 2002 Abstract Familial hemiplegic migraine (FHM) is a rare autosomal dominantly inherited subtype of migraine with aura. The clinical...

... channel gene are associated with familial hemiplegic migraine, episodic or progressive ataxia, coma and epilepsy. Future developments are likely to include the discovery of other ion channel genes associated with inherited and sporadic CNS disorders. The full range of manifestations of inherited ion...

... University Press 2000 2000 Abstract Neurotransmitter release at many synapses is regulated by P/Q-type Ca²⁺ channels containing the α_1A pore-forming subunit. Mutations in α_1A cause cerebral disorders including familial hemiplegic migraine (FHM) and ataxia in humans...

...Oxford University Press Migraine subtypes include probable migraine, hemiplegic migraine, migraine with brainstem aura (MWBA), retinal migraine, visual snow, vestibular migraine, and postictal headache. Probable migraine meets all the criteria but one for migraine with or without aura. Hemiplegic...

...; and (5) hemiplegic migraine; basilar migraine; frequent, prolonged or uncomfortable aura symptoms; or a history of migrainous infarction. prevention chronic migraine hemiplegic migraine basilar migraine migrainous infarction aura Preventive treatment Silberstein S D Topiramate Atenolol ß...

... disorders (channelopathies) are either hereditary or autoimmune. Phenotypes of hereditary channelopathies are usually paroxysmal or episodic disorders such as hereditary epilepsies, familial hemiplegic migraine, startle disease, episodic ataxia, and periodic paralysis. hereditary channelopathies familial...

...Oxford University Press Migraine is a complex neurological disorder with a strong genetic basis. Familial hemiplegic migraine is a classic monogenic subtype of which there are three well defined genes implicated. There are also a number of monogenic disorders where migraine is a prominent clinical...

... be categorized as channel disorders. Ion channel disorders hereditary channelopathy familial hemiplegic migraine hereditary epilepsy periodic paralysis autoimmune channelopathy myasthenia gravis Lambert-Eaton syndrome Isaacs syndrome Ataxia Channelopathies Genetic heterogeneity Hereditary startle...

...Oxford University Press Hemiplegic migraine (HM) is a rare monogenic subtype of migraine with aura that includes reversible motor weakness and can be either familial or sporadic. Three genes have been associated with HM. Migraine can also be part of more elaborate monogenic syndromes. When...

... disorders of childhood, discuss the neurobiology of headache, and review clinical presentation, diagnostic workup, and treatment. migraine headache trigeminal neuralgia botox topiramate hemiplegic migraine tension headache Abdominal migraine Basilar migraine Benign paroxysmal torticollis Benign...