Argitalpenak (17) Ikertzaileren baten partaidetza izan duten argitalpenak

1999

  1. 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

  2. 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

  3. 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

  4. Calpainopathy - A survey of mutations and polymorphisms

    American Journal of Human Genetics, Vol. 64, Núm. 6, pp. 1524-1540

  5. Central nervous system tuberculosis

    Neurologic Clinics, Vol. 17, Núm. 4, pp. 737-759

  6. Clinical correlation of striatal 1H MRS changes in Huntington's disease

    Neurology, Vol. 53, Núm. 4, pp. 806-812

  7. 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

  8. Distonia paroxistica sintomatica (variedad acinesigenica): Dos nuevos casos

    Neurologia, Vol. 14, Núm. 4, pp. 190-192

  9. Epilepsia y genética

    Trastornos adictivos: Organo Oficial de la Sociedad española de Toxicomanías, Vol. 1, Núm. 3, pp. 165-172

  10. La resonancia magnetica en el estudio de la tuberculosis espinal

    Radiologia, Vol. 41, Núm. 5, pp. 357-362

  11. Marchiafava-Bignami disease with widespread extracallosal lesions and favourable course

    Neuroradiology, Vol. 41, Núm. 1, pp. 40-43

  12. 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

  13. Procedural learning is impaired in patients with prefrontal lesions

    Neurology, Vol. 52, Núm. 9, pp. 1853-1860

  14. 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

  15. 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

  16. The challenge of drug-induced aseptic meningitis

    Archives of Internal Medicine, Vol. 159, Núm. 11, pp. 1185-1194

  17. 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