Publicaciones en colaboración con investigadores/as de Complejo Asistencial Universitario de Burgos (14)

2023

  1. Seizure prophylaxis in meningiomas: A systematic review and meta-analysis

    Neurologia, Vol. 38, Núm. 4, pp. 291-302

2021

  1. Exome-wide rare variant analysis in familial essential tremor

    Parkinsonism and Related Disorders, Vol. 82, pp. 109-116

  2. Volumetric growth rate of incidental asymptomatic meningiomas: a single-center prospective cohort study

    Acta Neurochirurgica, Vol. 163, Núm. 6, pp. 1665-1675

2020

  1. Vancomycin powder for the prevention of surgical site infection in posterior elective spinal surgery

    Neurocirugia, Vol. 31, Núm. 2, pp. 64-75

2019

  1. Cauda equina syndrome due to disk herniation: Long-term functional prognosis

    Neurocirugia, Vol. 30, Núm. 6, pp. 278-287

  2. Globular glial tauopathy caused by MAPT P301T mutation: clinical and neuropathological findings

    Journal of Neurology, Vol. 266, Núm. 10, pp. 2396-2405

2018

  1. Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48)

    Neurology, Vol. 91, Núm. 21, pp. E1988-E1998

  2. Papel de la cirugía en el tratamiento de las espondilodiscitis espontáneas: experiencia en 83 casos consecutivos

    Neurocirugia, Vol. 29, Núm. 2, pp. 64-78

  3. Pleiotropic effects of variants in dementia genes in Parkinson disease

    Frontiers in Neuroscience, Vol. 12, Núm. APR

  4. Pooled-DNA target sequencing of Parkinson genes reveals novel phenotypic associations in Spanish population

    Neurobiology of Aging, Vol. 70, pp. 325.e1-325.e5

  5. Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variants

    Neurobiology of Aging, Vol. 66, pp. 177.e7-177.e10

2017

  1. Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

    Journal of Neural Transmission, Vol. 124, Núm. 3, pp. 285-291

2015

  1. Association between Vitamin D receptor rs731236 (Taq1) polymorphism and risk for restless legs syndrome in the Spanish caucasian population

    Medicine (United States), Vol. 94, Núm. 47, pp. e2125

  2. Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome

    Medicine (United States), Vol. 94, Núm. 34, pp. e1448