Publications (47) Publications in which a researcher has participated

2012

  1. A predictive clinical-genetic model of tissue plasminogen activator response in acute ischemic stroke

    Annals of Neurology, Vol. 72, Núm. 5, pp. 716-729

  2. Age at onset in LRRK2-associated PD is modified by SNCA variants

    Journal of Molecular Neuroscience, Vol. 48, Núm. 1, pp. 245-247

  3. Alteration in cell cycle-related proteins in lymphoblasts from carriers of the c.709-1G>A PGRN mutation associated with FTLD-TDP dementia

    Neurobiology of Aging, Vol. 33, Núm. 2, pp. 429.e7-429.e20

  4. Analysis of antibodies to surface epitopes of contactin-2 in multiple sclerosis

    Journal of Neuroimmunology, Vol. 244, Núm. 1-2, pp. 103-106

  5. Botulinum toxin A in chronic refractory migraine: Premarketing experience

    Revista de Neurologia, Vol. 55, Núm. 7, pp. 385-391

  6. Brain transcriptomic profiling in idiopathic and LRRK2-associated Parkinson's disease

    Brain Research, Vol. 1466, pp. 152-157

  7. Brown-sequard syndrome after endovascular embolization of vertebral hemangioma

    Spinal Cord, Vol. 50, Núm. 8, pp. 636-637

  8. C3KO mouse expression analysis: Downregulation of the muscular dystrophy Ky protein and alterations in muscle aging

    Neurogenetics, Vol. 13, Núm. 4, pp. 347-357

  9. Cellular programming and reprogramming: Sculpting cell fate for the production of dopamine neurons for cell therapy

    Stem Cells International

  10. Chitinase 3-like 1 plasma levels are increased in patients with progressive forms of multiple sclerosis

    Multiple Sclerosis Journal, Vol. 18, Núm. 7, pp. 983-990

  11. Chronic migraine: A therapeutic challenge for clinicians

    Expert Opinion on Emerging Drugs, Vol. 17, Núm. 4, pp. 445-447

  12. Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: A case report

    Journal of Medical Case Reports, Vol. 6

  13. Current mutation discovery approaches in Retinitis Pigmentosa

    Vision Research, Vol. 75, pp. 117-129

  14. Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia

    Human Genetics, Vol. 131, Núm. 3, pp. 435-442

  15. Guía clínica de la enfermedad de pompe de inicio tardío

    Revista de Neurologia, Vol. 54, Núm. 8, pp. 497-507

  16. HLA-DRB1*15:01 and multiple sclerosis: A female association?

    Multiple Sclerosis Journal, Vol. 18, Núm. 5, pp. 569-577

  17. IL1B and VWF variants are associated with fibrinolytic early recanalization in patients with ischemic stroke

    Stroke, Vol. 43, Núm. 10, pp. 2659-2665

  18. Impact of apathy on health-related quality of life in recently diagnosed Parkinson's disease: The ANIMO study

    Movement Disorders, Vol. 27, Núm. 2, pp. 211-218

  19. Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3

    Human Molecular Genetics, Vol. 21, Núm. 14, pp. 3193-3204

  20. Inactivation of CDK/pRb pathway normalizes survival pattern of lymphoblasts expressing the FTLD-progranulin mutation c.709-1G>A

    PLoS ONE, Vol. 7, Núm. 5