Sporadic and familial hemiplegic migraine: Pathophysiological mechanisms, clinical characteristics, diagnosis, and management

The Lancet Neurology

Volumn 10, Issue 5, 2011, Pages 457-470

  Russell, Michael Bjørn ^a,b   Ducros, Anne ^c  

^a AKERSHUS UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF OSLO   (Norway)

^c HÔPITAL LARIBOISIÈRE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ACETAZOLAMIDE; ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); ATP1A2 PROTEIN; BOTULINUM TOXIN A; CACNA1A PROTEIN; CALCITONIN GENE RELATED PEPTIDE; DICHLORALPHENAZONE PLUS ISOMETHEPTENE MUCATE PLUS PARACETAMOL; DIHYDROERGOTAMINE; EXCITATORY AMINO ACID TRANSPORTER; ISOMETHEPTENE MUCATE; KETAMINE; LAMOTRIGINE; NIMODIPINE; SODIUM CHANNEL NAV1.1; TRIPTAN DERIVATIVE; UNCLASSIFIED DRUG; VERAPAMIL; VOLTAGE GATED CALCIUM CHANNEL;

ATAXIA; BLINDNESS; BRAIN ELECTROPHYSIOLOGY; CEREBELLAR ATAXIA; CEREBELLUM DISEASE; CEREBROSPINAL FLUID ANALYSIS; CHEMOPROPHYLAXIS; COMA; COMPUTER ASSISTED TOMOGRAPHY; CONSCIOUSNESS DISORDER; DIFFERENTIAL DIAGNOSIS; DISEASE SEVERITY; DOMINANT INHERITANCE; DOPPLER ECHOGRAPHY; DRUG EFFICACY; ELECTROENCEPHALOGRAM; ELICITED REPETITIVE DAILY BLINDNESS; EPILEPSY; FAMILIAL HEMIPLEGIC MIGRAINE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; HEADACHE; HEMIPARESIS; HUMAN; ION TRANSPORT; MEDICAL HISTORY; MENTAL DEFICIENCY; MIGRAINE WITH AURA; MIGRAINE WITHOUT AURA; MUSCLE WEAKNESS; NERVE CELL EXCITABILITY; NEUROPATHOLOGY; NONHUMAN; NUCLEAR MAGNETIC RESONANCE IMAGING; OFF LABEL DRUG USE; PATHOPHYSIOLOGY; PREVALENCE; PRIORITY JOURNAL; PROTEIN FUNCTION; REVIEW; SEIZURE; SPORADIC HEMIPLEGIC MIGRAINE; SPREADING CORTICAL DEPRESSION; TRANSITIONAL BLINDNESS; TRIGGER POINT;

DIAGNOSIS, DIFFERENTIAL; DISEASE MANAGEMENT; HUMANS; MIGRAINE WITH AURA;

EID: 79954880590     PISSN: 14744422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1474-4422(11)70048-5     Document Type: Review

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