Oriel Carreño

Affiliations: 
2006-2011 Genetics, Microbiology and Statistics University of Barcelona, Spain 
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"Oriel Carreño"
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Sintas C, Carreño O, Fernàndez-Castillo N, et al. (2017) Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia. Scientific Reports. 7: 2514
Vila-Pueyo M, Pons R, Raspall-Chaure M, et al. (2014) Clinical and genetic analysis in alternating hemiplegia of childhood: ten new patients from Southern Europe. Journal of the Neurological Sciences. 344: 37-42
Carreño O, Corominas R, Serra SA, et al. (2013) Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies. Molecular Genetics & Genomic Medicine. 1: 206-22
Sintas C, Carreño O, Fernández-Morales J, et al. (2012) A replication study of a GWAS finding in migraine does not identify association in a Spanish case-control sample. Cephalalgia : An International Journal of Headache. 32: 1076-80
Carreño O, Corominas R, Fernández-Morales J, et al. (2012) SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 94-103
Carreño O, García-Silva MT, García-Campos Ó, et al. (2011) Acute striatal necrosis in hemiplegic migraine with de novo CACNA1A mutation. Headache. 51: 1542-6
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