Publicaciones en las que colabora con José Ángel Berciano (13)

2018

  1. Enfermedades degenerativas motoras y cerebelosas

    Neurología (Elsevier), pp. 569-582

2017

  1. Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain

    Scientific Reports, Vol. 7, Núm. 1

2013

  1. Genetic variability related to serum uric acid concentration and risk of Parkinson's disease

    Movement Disorders, Vol. 28, Núm. 12, pp. 1737-1740

2011

  1. Genetic variation in α-synuclein kinases (CK-2β and GRK-5) and risk of Parkinson's disease

    Parkinsonism and Related Disorders

2005

  1. Genetics of Charcot-Marie-Tooth disease type 4A: Mutations, inheritance, phenotypic variability, and founder effect

    Journal of Medical Genetics, Vol. 42, Núm. 4, pp. 358-365

2002

  1. Candidate gene association studies in sporadic Alzheimer's disease

    Dementia and Geriatric Cognitive Disorders, Vol. 14, Núm. 1, pp. 41-54

2001

  1. Presente y futuro de la neurología Española

    Neurologia, Vol. 16, Núm. 9, pp. 408-417

  2. The -491 TT apolipoprotein E promoter polymorphism is associated with reduced risk for sporadic Alzheimer's disease

    Neuroscience Letters, Vol. 304, Núm. 3, pp. 204-208

  3. The Glu298Asp polymorphism in the NOS3 gene is not associated with sporadic Alzheimer's disease [4]

    Journal of Neurology Neurosurgery and Psychiatry

2000

  1. Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD

    Neurology, Vol. 55, Núm. 4, pp. 593-595

1999

  1. 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

1991

  1. High-affinity choline uptake carrier in Alzheimer's disease: implications for the cholinergic hypothesis of dementia

    Brain Research, Vol. 552, Núm. 1, pp. 170-174

1990

  1. Esclerosis múltiple o enfermedad de Lyme? Un problema diagnóstico de exclusión.

    Medicina clinica, Vol. 94, Núm. 18, pp. 685-688