Publicaciones en las que colabora con José Felix Martí Massó (111)

2020

  1. The Discovery of the Dardarin Gene 15 Years Later: A Globalized Local History

    Movement Disorders

2018

  1. El cuidado paliativo del enfermo neurológico agudo

    Medicina paliativa: cuidados del enfermo en el final de la vida y atención a su familia (EUNSA. Ediciones Universidad de Navarra, S.A.), pp. 253-271

  2. Familial amyloidosis with polyneuropathy type 1 caused by transthyretin mutation Val50Met (Val30Met): 4 cases in a non-endemic area

    Neurologia, Vol. 33, Núm. 9, pp. 583-589

  3. Reversible delayed post-hypoxic leukoencephalopathy

    Neurologia

2017

  1. Headache and other complications following intrathecal chemotherapy administration

    Cephalalgia

  2. Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease

    European Journal of Neurology, Vol. 24, Núm. 2, pp. 427-e6

  3. Tau/α-synuclein ratio and inflammatory proteins in Parkinson's disease: An exploratory study

    Movement Disorders, Vol. 32, Núm. 7, pp. 1066-1073

  4. The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics

    PLoS ONE, Vol. 12, Núm. 6

  5. Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease

    Neurology: Genetics, Vol. 3, Núm. 5

  6. ¿Son la forma precoz y la de presentación tardía la misma enfermedad de Parkinson?

    Revista española de trastornos del movimiento, Vol. 9, Núm. 1, pp. 6-11

2016

  1. Congenital Spinal Malformation and Stroke: Aneurysmal Dilatations and Bilateral Rotational Vertebral Artery Occlusion

    Journal of Stroke and Cerebrovascular Diseases, Vol. 25, Núm. 3, pp. e23-e24

  2. DAT imaging and clinical biomarkers in relatives at genetic risk for LRRK2R1441G Parkinson's disease

    Movement Disorders, Vol. 31, Núm. 3, pp. 335-343

  3. Genetic Mutation Analysis of Parkinson’s Disease Patients Using Multigene Next-Generation Sequencing Panels

    Molecular Diagnosis and Therapy, Vol. 20, Núm. 5, pp. 481-491

  4. Inflammatory profile in LRRK2-associated prodromal and clinical PD

    Journal of Neuroinflammation, Vol. 13, Núm. 1

  5. Rombencefalitis y endocarditis por listeria monocytogenes: Una asociación no descrita

    Revista de Neurologia

  6. Selection of entropy based features for automatic analysis of essential tremor

    Entropy, Vol. 18, Núm. 5

2015

  1. Autonomic involvement in Parkinsonian carriers of PARK2 gene mutations

    Parkinsonism and Related Disorders, Vol. 21, Núm. 7, pp. 717-722

  2. Clinical correlations with lewy body pathology in LRRK2-related Parkinson disease

    JAMA Neurology, Vol. 72, Núm. 1, pp. 100-105

  3. GIGYF2 mutation in late-onset Parkinson's disease with cognitive impairment

    Journal of Human Genetics, Vol. 60, Núm. 10, pp. 637-640

  4. Higher frequency of certain cancers in LRRK2 G2019S mutation carriers with Parkinson disease a pooled analysis

    JAMA Neurology, Vol. 72, Núm. 1, pp. 58-65