Association between the G1246A polymorphism of the hypocretin receptor 2 gene and cluster headache : a meta-analysis
- Author
- RAINERO, Innocenzo1 ; RUBINO, Elisa1 ; VALFRE, Walter1 ; GALLONE, Salvatore1 ; DE MARTINO, Paola1 ; ZAMPELLA, Erika1 ; PINESSI, Lorenzo1
[1] Neurology II -Headache Centre, Department of Neuroscience, University of Turin Via Cherasco 15, 10126 Torino, Italy - Source
The Journal of headaches and pain (Testo stampato). 2007, Vol 8, Num 3, pp 152-156, 5 p ; ref : 25 ref
- Publisher
- Springer, Milano
- Publication country
- Italy
- Document type
- Article
- Language
- English
- Author keyword
- Cluster headache G1246A polymorphism Genetic association Hypocretin receptor 2 gene Meta-analysis
- Keyword (fr)
- Analyse amas Céphalée vasomotrice Horton Céphalée Cérébrovasculaire pathologie Douleur Effet aléatoire Etude cas témoin Facteur risque Génotype Modèle Polymorphisme Porteur Système nerveux pathologie Récepteur orexine Appareil circulatoire pathologie Encéphale pathologie Système nerveux central pathologie Trouble neurologique Vaisseau sanguin pathologie
- Keyword (en)
- Cluster analysis Cluster headache Headache Cerebrovascular disease Pain Random effect Case control study Risk factor Genotype Models Polymorphism Carrier Nervous system diseases Orexin receptor Cardiovascular disease Cerebral disorder Central nervous system disease Neurological disorder Vascular disease
- Keyword (es)
- Analisis cluster Cefalea vasomotriz Horton Cefalea Vaso sanguíneo encéfalo patología Dolor Efecto aleatorio Estudio caso control Factor riesgo Genotipo Modelo Polimorfismo Portador Sistema nervioso patología Aparato circulatorio patología Encéfalo patología Sistema nervosio central patología Trastorno neurológico Vaso sanguíneo patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17A Nervous system (semeiology, syndromes) / 002B17A03 Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17C Vascular diseases and vascular malformations of the nervous system
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B17 Neurology / 002B17G Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases
- Discipline
- Neurology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 19005368
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1007/s10194-007-0383-x 
https://dx.doi.org/10.1007/s10194-007-0383-x
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