Especialidad
Neurología
Publicaciones (47) Publicaciones en las que ha participado algún/a investigador/a
2012
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A predictive clinical-genetic model of tissue plasminogen activator response in acute ischemic stroke
Annals of Neurology, Vol. 72, Núm. 5, pp. 716-729
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Age at onset in LRRK2-associated PD is modified by SNCA variants
Journal of Molecular Neuroscience, Vol. 48, Núm. 1, pp. 245-247
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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
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Analysis of antibodies to surface epitopes of contactin-2 in multiple sclerosis
Journal of Neuroimmunology, Vol. 244, Núm. 1-2, pp. 103-106
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Botulinum toxin A in chronic refractory migraine: Premarketing experience
Revista de Neurologia, Vol. 55, Núm. 7, pp. 385-391
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Brain transcriptomic profiling in idiopathic and LRRK2-associated Parkinson's disease
Brain Research, Vol. 1466, pp. 152-157
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Brown-sequard syndrome after endovascular embolization of vertebral hemangioma
Spinal Cord, Vol. 50, Núm. 8, pp. 636-637
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C3KO mouse expression analysis: Downregulation of the muscular dystrophy Ky protein and alterations in muscle aging
Neurogenetics, Vol. 13, Núm. 4, pp. 347-357
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Cellular programming and reprogramming: Sculpting cell fate for the production of dopamine neurons for cell therapy
Stem Cells International
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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
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Chronic migraine: A therapeutic challenge for clinicians
Expert Opinion on Emerging Drugs, Vol. 17, Núm. 4, pp. 445-447
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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
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Current mutation discovery approaches in Retinitis Pigmentosa
Vision Research, Vol. 75, pp. 117-129
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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
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Guía clínica de la enfermedad de pompe de inicio tardío
Revista de Neurologia, Vol. 54, Núm. 8, pp. 497-507
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HLA-DRB1*15:01 and multiple sclerosis: A female association?
Multiple Sclerosis Journal, Vol. 18, Núm. 5, pp. 569-577
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IL1B and VWF variants are associated with fibrinolytic early recanalization in patients with ischemic stroke
Stroke, Vol. 43, Núm. 10, pp. 2659-2665
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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
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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
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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