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Titolo:
Genetics of primary headaches
Autore:
Kors, EE; Haan, J; Ferrari, MD;
Indirizzi:
Leiden Univ, Med Ctr, Dept Neurol, NL-2300 RC Leiden, Netherlands Leiden Univ Leiden Netherlands NL-2300 RC NL-2300 RC Leiden, Netherlands Rijnland Hosp, Dept Neurol, Leiderdorp, Netherlands Rijnland Hosp Leiderdorp Netherlands pt Neurol, Leiderdorp, Netherlands
Titolo Testata:
CURRENT OPINION IN NEUROLOGY
fascicolo: 3, volume: 12, anno: 1999,
pagine: 249 - 254
SICI:
1350-7540(199906)12:3<249:GOPH>2.0.ZU;2-V
Fonte:
ISI
Lingua:
ENG
Soggetto:
FAMILIAL HEMIPLEGIC MIGRAINE; POTASSIUM CHANNEL GENE; DRD2 NCOI ALLELES; CLUSTER HEADACHE; NUCLEOTIDE PAIR-11084; TYPICAL MIGRAINE; EPISODIC ATAXIA; AURA; MUTATION; EPILEPSY;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Citazioni:
44
Recensione:
Indirizzi per estratti:
Indirizzo: Ferrari, MD Leiden Univ, Med Ctr, Dept Neurol, K5Q,POB 9600, NL-2300 RC Leiden, Netherlands Leiden Univ K5Q,POB 9600 Leiden Netherlands NL-2300 RC rlands
Citazione:
E.E. Kors et al., "Genetics of primary headaches", CURR OP NEU, 12(3), 1999, pp. 249-254

Abstract

Migraine has become an important topic in the field of complex genetic disorders. The identification of a gene on chromosome 19p encoding for an alpha 1A calcium channel subunit causing familiar hemiplegic migraine has led to the classification of migraine as a channelopathy. More recently, effortshave been made to clarify the genetics of other primary headaches. (C) 1999 Lippincott Williams & Wilkins.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 01/04/20 alle ore 20:37:27