Publicacions en col·laboració amb investigadors/es de Radboud University Nijmegen Medical Centre (12)

2021

  1. Toward e-Scales: Digital Administration of the International Parkinson and Movement Disorder Society Rating Scales

    Movement Disorders Clinical Practice, Vol. 8, Núm. 2, pp. 208-214

2020

  1. Implementation of Telemedicine for Urgent and Ongoing Healthcare for Patients with Parkinson's Disease During the COVID-19 Pandemic: New Expectations for the Future

    Journal of Parkinson's disease

2019

  1. Clinical and genetic characteristics of late-onset Huntington's disease

    Parkinsonism and Related Disorders, Vol. 61, pp. 101-105

2018

  1. Population genomics of Mesolithic Scandinavia: Investigating early postglacial migration routes and high-latitude adaptation

    PLoS Biology, Vol. 16, Núm. 1

  2. Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study

    Journal of Huntington's Disease, Vol. 7, Núm. 3, pp. 209-222

  3. Telemedicine Use for Movement Disorders: A Global Survey

    Telemedicine and e-Health, Vol. 24, Núm. 12, pp. 979-992

2014

  1. The past, present, and future of telemedicine for Parkinson's disease

    Movement Disorders, Vol. 29, Núm. 7, pp. 871-883

2013

  1. The V471A Polymorphism in Autophagy-Related Gene ATG7 Modifies Age at Onset Specifically in Italian Huntington Disease Patients

    PLoS ONE, Vol. 8, Núm. 7

  2. β-defensin genomic copy number does not influence the age of onset in huntington’s disease

    Journal of Huntington's Disease, Vol. 2, Núm. 1, pp. 107-124

2012

  1. Discrepancies in reporting the CAG repeat lengths for Huntington’s disease

    European Journal of Human Genetics, Vol. 20, Núm. 1, pp. 20-26

2011

  1. Activation of human neutrophils by oleic acid involves the production of reactive oxygen species and a rise in cytosolic calcium concentration: A comparison with N-6 polyunsaturated fatty acids

    Cellular Physiology and Biochemistry, Vol. 28, Núm. 2, pp. 329-338

  2. NMDA receptor gene variations as modifiers in Huntington disease: A replication study

    PLoS Currents