Skip to search formSkip to main contentSkip to account menu

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.
Review
2020
Review
2020
Diagnostic and therapeutic aspects of hemiplegic migraine
Hemiplegic migraine (HM) is a clinically and genetically heterogeneous condition with attacks of headache and motor weakness… 
Highly Cited
2018
Highly Cited
2018
Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation
Objective To investigate whether the clinical characteristics of patients with hemiplegic migraine with and without autosomal… 
2014
2014
PRRT2 and hemiplegic migraine: A complex association
Hemiplegic migraine (HM) is a rare migraine subtype characterized by hemiparesis during the attack and is associated with at… 
Highly Cited
2012
Highly Cited
2012
PRRT2 mutations cause hemiplegic migraine
ABSTRACT Objective: Hemiplegic migraine (HM) is a rare subtype of migraine with aura that occurs as a familial or sporadic… 
Highly Cited
2012
Highly Cited
2012
Familial PRRT2 mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine
PRRT2 is the gene recently associated with paroxysmal kinesigenic dyskinesia (PKD), benign familial infantile epilepsy, and… 
2012
2012
Safety and efficacy of flunarizine in childhood migraine: 11 years’ experience, with emphasis on its effect in hemiplegic migraine
Aim  The aim of this study was to report a single‐centre experience of flunarizine in childhood migraine with focus on safety and… 
Highly Cited
2010
Highly Cited
2010
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
Objective: Hemiplegic migraine (HM) is a rare subtype of migraine with aura that may occur as a familial (FHM) or sporadic… 
Review
2002
Review
2002
An Epidemiological Survey of Hemiplegic Migraine
The objective of the present study was to use systematic nation-wide case-finding methods to establish the prevalence and sex… 
Highly Cited
2002
Highly Cited
2002
Distal myopathy with tubular aggregates: a new phenotype associated with multiple deletions in mitochondrial DNA?
WEMINO (wall eyed monocular internuclear ophthalmoplegia) syndrome is a rare neurological impairment involving disconjugate… 
Highly Cited
1999
Highly Cited
1999
Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.
Familial hemiplegic migraine (HM) is an autosomal dominant migraine with aura. In 20% of HM families, HM is associated with a… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)