Publicaciones (25) Publicaciones en las que ha participado algún/a investigador/a

1999

  1. Amoxicillin can induce aseptic meningitis - In reply

    ARCHIVES OF INTERNAL MEDICINE

  2. Amoxicillin can induce aseptic meningitis [3]

    Archives of Internal Medicine

  3. 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

  4. 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

  5. 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

  6. Calpain deficiency in Spain and Aquitania

    Acta Myologica

  7. Calpainopathies in Spain, the Spanish study

    Acta Myologica

  8. Calpainopathy - A survey of mutations and polymorphisms

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

  9. Central nervous system tuberculosis

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

  10. Cinnarizine-induced parkinsonism: Ten years later (multiple letters) [1]

    Movement Disorders

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

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

  12. 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

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

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

  14. Distrofia muscular de cinturas: Un sindrome clinica y geneticamente heterogeneo

    Neurologia

  15. Epilepsia y genética

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

  16. Erratum: Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkBa/NF-κB pathway in limb-girdle muscular dystrophy type 2A (Nature Medicine (1999) 5 (503-511))

    Nature Medicine

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

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

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

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

  19. Miositis idiopáticas: enfermedad o síndrome?

    Medicina clínica

  20. 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