Publicaciones en las que colabora con José Felix Martí Massó (10)

2006

  1. Apolipoprotein E ε4 allele in familial and sporadic Parkinson's disease

    Neuroscience Letters, Vol. 406, Núm. 3, pp. 235-239

  2. Parkinson's disease due to the R1441G mutation in Dardarin: A founder effect in the Basques

    Movement Disorders, Vol. 21, Núm. 11, pp. 1954-1959

2005

  1. Familial Parkinson's disease: Clinical and genetic analysis of four Basque families

    Annals of Neurology, Vol. 57, Núm. 3, pp. 365-372

  2. LGMD2A: Genotype-phenotype correlations based on a large mutational survey on the calpain 3 gene

    Brain, Vol. 128, Núm. 4, pp. 732-742

2004

  1. Mitochondrial polymporphisms in Parkinson's Disease

    Neuroscience Letters, Vol. 370, Núm. 2-3, pp. 171-174

2002

  1. Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy

    Human Molecular Genetics, Vol. 11, Núm. 9, pp. 1119-1128

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

1998

  1. Limb-girdle muscular dystrophy in Guipuzcoa (Basque Country, Spain)

    Brain, Vol. 121, Núm. 9, pp. 1735-1747

1996

  1. Frequency of intergenerational contractions of the CTG repeats in myotonic dystrophy

    Genetic Epidemiology, Vol. 13, Núm. 5, pp. 483-487

  2. Frequency of myotonic dystrophy gene carriers in cataract patients

    Journal of Medical Genetics, Vol. 33, Núm. 3, pp. 221-223