Publicaciones en las que colabora con Renée Ribacoba Montero (18)

2019

  1. HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease

    Neurobiology of Aging, Vol. 76, pp. 215.e9-215.e14

2014

  1. Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms

    Neuroscience Letters, Vol. 562, pp. 45-49

  2. MiRNA Profile in the Substantia Nigra of Parkinson’s Disease and Healthy Subjects

    Journal of Molecular Neuroscience, Vol. 54, Núm. 4, pp. 830-836

  3. The screening of the 3′UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson's disease

    Journal of Human Genetics, Vol. 59, Núm. 6, pp. 346-348

2013

  1. Mutational screening of PARKIN identified a 3′ UTR variant (rs62637702) associated with parkinson's disease

    Journal of Molecular Neuroscience, Vol. 50, Núm. 2, pp. 264-269

  2. Profile of microRNAs in the plasma of Parkinson's disease patients and healthy controls

    Journal of Neurology

2012

  1. A search for SNCA 3′ UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease

    Journal of Molecular Neuroscience, Vol. 47, Núm. 3, pp. 425-430

2010

  1. Analysis of the micro-RNA-133 and PITX3 genes in Parkinson's disease

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 6, pp. 1234-1239

  2. FGF20 rs12720208 SNP and microRNA-433 variation: No association with Parkinson's disease in Spanish patients

    Neuroscience Letters, Vol. 479, Núm. 1, pp. 22-25

  3. Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia

    BMC Neurology, Vol. 10

2007

  1. Delayed posterior encephalopathy syndrome following chemotherapy with oxaliplatin and gemcitabine [3]

    Journal of Neurology

2006

  1. LRRK2 mutations are a common cause of Parkinson's disease in Spain

    European Journal of Neurology, Vol. 13, Núm. 4, pp. 391-394

  2. Trigeminal mononeuropathy: First clinical manifestation of breast cancer [1]

    European Neurology

2005

  1. Acute deafness as an extraintestinal manifestation of ulcerative colitis

    European Journal of Internal Medicine, Vol. 16, Núm. 6, pp. 440-442

2001

  1. SUNCT syndrome and seborrheic dermatitis associated with craneosynostosis

    Cephalalgia, Vol. 21, Núm. 2, pp. 157-159

1999

  1. Angiotensin converting enzyme and endothelial nitric oxide synthase DNA polymorphisms and late onset Alzheimer's disease

    Journal of Neurology Neurosurgery and Psychiatry, Vol. 67, Núm. 6, pp. 733-736

  2. Association between an α2 macroglobulin DNA polymorphism and late-onset Alzheimer's disease

    Biochemical and Biophysical Research Communications, Vol. 264, Núm. 1, pp. 48-50

  3. Frecuencia del alelo APOE-4 en la enfermedad de Alzheimer en la población asturiana y su variación con la edad

    Medicina Clinica, Vol. 113, Núm. 12, pp. 441-443