Especialidad
Neurología
Publicaciones (17) Publicaciones en las que ha participado algún/a investigador/a
1999
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Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large Basque pedigree linked to chromosome 10q
Annals of Neurology, Vol. 45, Núm. 2, pp. 182-188
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Autosomal dominant nocturnal frontal lobe epilepsy in a Spanish family with a Ser252Phe mutation in the CHRNA4 gene
Archives of Neurology, Vol. 56, Núm. 8, pp. 1004-1009
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Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A
Nature Medicine, Vol. 5, Núm. 5, pp. 503-511
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Calpainopathy - A survey of mutations and polymorphisms
American Journal of Human Genetics, Vol. 64, Núm. 6, pp. 1524-1540
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Central nervous system tuberculosis
Neurologic Clinics, Vol. 17, Núm. 4, pp. 737-759
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Clinical correlation of striatal 1H MRS changes in Huntington's disease
Neurology, Vol. 53, Núm. 4, pp. 806-812
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Diferencias en la imitación de diferentes tipos de movimientos en pacientes con probable enfermedad de Alzheimer.
Revista española de neuropsicología, Vol. 1, Núm. 1, pp. 29-48
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Distonia paroxistica sintomatica (variedad acinesigenica): Dos nuevos casos
Neurologia, Vol. 14, Núm. 4, pp. 190-192
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Epilepsia y genética
Trastornos adictivos: Organo Oficial de la Sociedad española de Toxicomanías, Vol. 1, Núm. 3, pp. 165-172
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La resonancia magnetica en el estudio de la tuberculosis espinal
Radiologia, Vol. 41, Núm. 5, pp. 357-362
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Marchiafava-Bignami disease with widespread extracallosal lesions and favourable course
Neuroradiology, Vol. 41, Núm. 1, pp. 40-43
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Polymorphisms in the presenilin 1 and presenilin 2 genes and risk for sporadic Alzheimer's disease
Journal of the Neurological Sciences, Vol. 171, Núm. 2, pp. 88-91
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Procedural learning is impaired in patients with prefrontal lesions
Neurology, Vol. 52, Núm. 9, pp. 1853-1860
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Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism
American Journal of Human Genetics, Vol. 65, Núm. 5, pp. 1437-1448
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The A1555G mutation in the 12S rRNA gene of human mtDNA: Recurrent origins and founder events in families affected by sensorineural deafness
American Journal of Human Genetics, Vol. 65, Núm. 5, pp. 1349-1358
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The challenge of drug-induced aseptic meningitis
Archives of Internal Medicine, Vol. 159, Núm. 11, pp. 1185-1194
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The plasminogen activation system enhances brain and heart invasion in murine relapsing fever borreliosis
Journal of Clinical Investigation, Vol. 103, Núm. 1, pp. 81-87