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Volumn 13, Issue 7, 2010, Pages 467-471
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Calcium channelopathies in inherited neurological disorders: Relevance to drug screening for acquired channel disorders
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Author keywords
Ataxia; autism; calcium channel; channelopathy; epilepsy; gene mutation; migraine; neurological disorder; VGCC; voltage gated calcium channel
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Indexed keywords
4 AMINOPYRIDINE;
ACETAZOLAMIDE;
ANTICONVULSIVE AGENT;
FLUNARIZINE;
VOLTAGE GATED CALCIUM CHANNEL;
CALCIUM CHANNEL;
ABSENCE;
ATAXIA;
AUTISM;
BIPOLAR DISORDER;
CALCIUM CHANNELOPATHY;
DRUG SCREENING;
EPILEPSY;
FAMILIAL HEMIPLEGIC MIGRAINE;
GENE MUTATION;
GENETIC RISK;
HUMAN;
MIGRAINE;
MIGRAINE WITH AURA;
NEUROLOGIC DISEASE;
NONHUMAN;
REVIEW;
SPINOCEREBELLAR DEGENERATION;
ANIMAL;
CHANNELOPATHIES;
DRUG DESIGN;
GENETICS;
NERVOUS SYSTEM DISEASES;
PATHOPHYSIOLOGY;
PROCEDURES;
ANIMALS;
CALCIUM CHANNELS;
CHANNELOPATHIES;
DRUG DESIGN;
DRUG EVALUATION, PRECLINICAL;
HUMANS;
NERVOUS SYSTEM DISEASES;
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EID: 77954140544
PISSN: 13697056
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (12)
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References (0)
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