Ictus Traslacional
Hospital Universitario de Donostia
San Sebastián, EspañaPublications in collaboration with researchers from Hospital Universitario de Donostia (14)
2024
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Description of clinical and genetic features of 122 patients included in the Spanish Pompe registry
Neuromuscular Disorders, Vol. 34, pp. 1-8
2022
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Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcome
Annals of Clinical and Translational Neurology, Vol. 9, Núm. 2, pp. 122-131
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Selection of patients for percutaneous closure in nonlacunar cryptogenic stroke associated with patent foramen ovale. Data from the NORDICTUS cooperative registry
Neurologia
2021
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Clinical characteristics and outcomes of thymoma-associated myasthenia gravis
European Journal of Neurology, Vol. 28, Núm. 6, pp. 2083-2091
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Impact of the COVID-19 pandemic on the training of Spanish neurology residents
Neurology Perspectives, Vol. 1, Núm. 2, pp. 124-130
2020
2019
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Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy
Journal of Neurology, Neurosurgery and Psychiatry, Vol. 90, Núm. 5, pp. 576-585
2017
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Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain
Scientific Reports, Vol. 7, Núm. 1
2015
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Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain
Brain
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Myasthenia gravis: Descriptive analysis of life-threatening events in a recent nationwide registry
European Journal of Neurology, Vol. 22, Núm. 7, pp. 1056-1061
2013
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Analysis of the C9orf72 Gene in Patients with Amyotrophic Lateral Sclerosis in Spain and Different Populations Worldwide
Human Mutation, Vol. 34, Núm. 1, pp. 79-82
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Using Leo Plus stent as flow diverter and endoluminal remodeling in endovascular treatment of intracranial fusiform aneurysms
Journal of NeuroInterventional Surgery, Vol. 5, Núm. SUPPL.3
2012
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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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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