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Current Neuropharmacology, ISSN 1570-159X, 2019, Volume 17, Issue 10, pp. 961 - 973
Journal Article
Journal of Clinical Neurophysiology, ISSN 0736-0258, 01/2018, Volume 35, Issue 1, pp. e3 - e7
INTRODUCTION:Familial hemiplegic migraine (FHM) is a genetic disease with a variable clinical phenotype. The imaging and electroencephalogram (EEG) correlates... 
Familial hemiplegic migraine | ATP1A2 | EEG | Encephalopathy | NEUROSCIENCES | SPREADING DEPRESSION | CLINICAL NEUROLOGY
Journal Article
Neurology, ISSN 0028-3878, 01/2018, Volume 90, Issue 7, pp. e575 - e582
OBJECTIVETo investigate whether the clinical characteristics of patients with hemiplegic migraine with and without autosomal dominant mutations in CACNA1A,... 
INDIVIDUALS | METAANALYSIS | CHANNEL | PRRT2 GENE | FAMILIAL MIGRAINE | SUSCEPTIBILITY LOCI | PAROXYSMAL KINESIGENIC DYSKINESIA | EPISODIC ATAXIA | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | PATHOPHYSIOLOGY
Journal Article
Cephalalgia, ISSN 0333-1024, 8/2014, Volume 34, Issue 9, pp. 708 - 711
Background Familial hemiplegic migraine (FHM) is a rare monogenic subtype of migraine with aura that includes motor auras. Prophylactic treatment of FHM often... 
familial hemiplegic migraine | ion transport | anticonvulsants | Migraine | neurogenetics | PROPHYLAXIS | ATTACKS | AURA | NEUROSCIENCES | CLINICAL NEUROLOGY
Journal Article
BBA - Biomembranes, ISSN 0005-2736, 07/2014, Volume 1838, Issue 7, pp. 1693 - 1700
Journal Article
Headache: The Journal of Head and Face Pain, ISSN 0017-8748, 06/2019, Volume 59, Issue 6, pp. 917 - 923
Objective To explore the neuropsychological correlates and implications of familial hemiplegic migraines (FHMs). Background FMH is a rare, autosomal dominant... 
neuropsychology | familial hemiplegic migraine | baseline testing | CLINICAL NEUROLOGY | Case studies | Migraine | Cerebellum | Headache | Psychology | Cognitive ability | Information processing | Impairment | Measuring techniques
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 09/2018, Volume 392, pp. 22 - 27
Familial hemiplegic migraine (FHM) is a rare monogenic form of migraine with aura with three distinct genetic subtypes (FHM1-3). Imaging studies during acute... 
Familial hemiplegic migraine | ATP1A2 | MRI | Perfusion | FHM2 | HYPERPERFUSION | MECHANISMS | NEUROSCIENCES | CLINICAL NEUROLOGY | PATHOPHYSIOLOGY | ENCEPHALOPATHY | EDEMA | MUTATION | BIPHASIC NEUROVASCULAR CHANGES | AURA | COMA | CT imaging | Genetic aspects | Diagnostic imaging | Migraine
Journal Article
Cephalalgia, ISSN 0333-1024, 11/2017, Volume 37, Issue 13, pp. 1294 - 1298
Background Familial hemiplegic migraine (FHM) is a rare type of migraine with aura that is characterized by transient hemiparesis. Mutations in three genes... 
familial hemiplegic migraine | SCN1A gene | China | Migraine | NEUROSCIENCES | CLINICAL NEUROLOGY | Young Adult | Migraine Disorders - genetics | Pedigree | Humans | Middle Aged | NAV1.1 Voltage-Gated Sodium Channel - genetics | Adolescent | Asian Continental Ancestry Group - genetics | Adult | Female | Male | Mutation, Missense
Journal Article
Cephalalgia, ISSN 0333-1024, 11/2014, Volume 34, Issue 13, pp. 1062 - 1069
Background Familial hemiplegic migraine (FHM) is a rare monogenic subtype of migraine with aura, characterized by motor auras. The majority of FHM families... 
familial hemiplegic migraine | SCN1A gene | Migraine | ion channel defects | Amino Acid Sequence | Humans | Middle Aged | NAV1.1 Voltage-Gated Sodium Channel - genetics | Molecular Sequence Data | Male | Young Adult | DNA Mutational Analysis | Pedigree | Adolescent | Age of Onset | Adult | Female | Aged | Migraine with Aura - genetics | Mutation | Child
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 12/2013, Volume 1832, Issue 12, pp. 2173 - 2179
Familial hemiplegic migraine (FHM) is a monogenic variant of migraine with aura. One of the three known causative genes, ATP1A2, which encodes the α2 isoform... 
Familial hemiplegic migraine | ATP1A2 | Domain interaction | Na,K-ATPase | FHM2 | α2 isoform | ATP1A2 MUTATION | GASTRIC H,K-ATPASE | ALPHA-SUBUNIT | CRYSTAL-STRUCTURE | ATPASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | HIGH-AFFINITY BINDING | SODIUM-POTASSIUM PUMP | BIOPHYSICS | AMINO-ACIDS | NA+,K+-ATPASE | alpha 2 isoform | EPILEPSY | Genetic aspects | Glutamate | Migraine | Adenosine triphosphatase | Glutamine | Index Medicus
Journal Article
CEPHALALGIA, ISSN 0333-1024, 11/2014, Volume 34, Issue 13, pp. 1062 - 1069
Background Familial hemiplegic migraine (FHM) is a rare monogenic subtype of migraine with aura, characterized by motor auras. The majority of FHM families... 
GENE-MUTATIONS | familial hemiplegic migraine | Migraine | SCNIA gene | NEUROSCIENCES | ion channel defects | CLINICAL NEUROLOGY | INACTIVATION | PRRT2 MUTATIONS | SODIUM-CHANNEL SCN1A | SEVERE MYOCLONIC EPILEPSY | PAROXYSMAL KINESIGENIC DYSKINESIA | EPISODIC ATAXIA
Journal Article