Detalhe da pesquisa
1.
Association study of the serotoninergic system in migraine in the Spanish population.
Am J Med Genet B Neuropsychiatr Genet
; 153B(1): 177-84, 2010 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19455600
2.
Lack of association of hormone receptor polymorphisms with migraine.
Eur J Neurol
; 16(3): 413-5, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19175383
3.
Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes.
Cephalalgia
; 28(10): 1039-47, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18644040
4.
[Congenital insensitivity to pain with anhidrosis associated with congenital myasthenic syndrome]. / Insensibilidad congénita al dolor con anhidrosis asociada a síndrome miasténico congénito.
Rev Neurol
; 41(4): 218-22, 2005.
Artigo
em Espanhol
| MEDLINE | ID: mdl-16075400
5.
[Hyperkalemic periodic paralysis: a Spanish family with the p.Thr704Met mutation in the SCN4A gene]. / Parálisis periódica hipercaliémica: presentación de una familia española con la mutación p.Thr704Met en el gen SCN4A.
Neurologia
; 23(7): 427-35, 2008 Sep.
Artigo
em Espanhol
| MEDLINE | ID: mdl-18726720
6.
Molybdenum cofactor deficiency presenting as neonatal hyperekplexia: a clinical, biochemical and genetic study.
Neuropediatrics
; 36(6): 389-94, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16429380
7.
Paroxysmal kinesigenic dyskinesia and generalized seizures: clinical and genetic analysis in a Spanish pedigree.
Neuropediatrics
; 33(6): 288-93, 2002 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-12571782