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Hemiplegic migraines

Known as: Hemiplegic migraine 
National Institutes of Health

Related topics

Related topics

1 relation
Phosphoglycerate Kinase 1 Deficiency

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
A retrospective analysis of triptan and dhe use for basilar and hemiplegic migraine
Patients with basilar migraine (BM) and hemiplegic migraine (HM) have been excluded from triptan and DHE clinical trials due to a… 
2013
2013
PRRT2 mutation causes paroxysmal kinesigenic dyskinesia and hemiplegic migraine in monozygotic twins.
2012
2012
Complex migraine with subtherapeutic INR in antiphospholipid syndrome.
2011
2011
The digiti quinti sign in hemiplegic migraine
The digiti quinti sign (DQS), described originally as a clinical indication of subtle motor deficit, consists of a relatively… 
Review
2011
Review
2011
A novel mutation in CACNA1A associated with hemiplegic migraine, cerebellar dysfunction and late-onset cognitive decline
2010
2010
Link between confusional migraine, hemiplegic migraine and episodic ataxia type 2: Hypothesis, family genealogy, gene typing and classification
An association between hemiplegic migraine (HM) and episodic ataxia type 2 (EA2) has been described; both disorders are linked to… 
2007
2007
Adult-Onset Hemiplegic Migraine with Cortical Enhancement and Oedema
We present genetically identical twin patients who experienced late-onset migraine with visual and somatosensory auras and later… 
2007
2007
Amino acid changes in the amino terminus of the Na,K‐adenosine triphosphatase alpha‐2 subunit associated to familial and sporadic hemiplegic migraine
Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura inherited with an autosomal dominant pattern. Here, we… 
2006
2006
Hemiplegic Migraine: Clinical Features, Links with Basilar‐type Migraine, Current and Future Treatment
Hemiplegic migraine (HM) is a rare variety of migraine with aura characterized by the presence of a motor weakness during the… 
2006
2006
The identification of a recurrent phosphoglycerate kinase mutation associated with chronic haemolytic anaemia and neurological dysfunction in a family from USA
Phosphoglycerate kinase (PGK) deficiency is a rare X‐linked disease that is characterised by mild to severe haemolytic anaemia… 
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