IDOIA
ROUCO AXPE
Hospital de Cruces
Barakaldo, EspañaPublications en collaboration avec des chercheurs de Hospital de Cruces (22)
2024
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Practical recommendations for the clinical evaluation of patients with hereditary ataxia and hereditary spastic paraplegia
Neurologia, Vol. 39, Núm. 6, pp. 515-522
2023
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Epidemiology of ataxia and hereditary spastic paraplegia in Spain: a cross-sectional study
Neurologia, Vol. 38, Núm. 6, pp. 379-386
2022
2021
2016
2015
2014
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Cerebellar ataxia and glutamic acid decarboxylase antibodies: Immunologic profile and long-term effect of immunotherapy
JAMA Neurology, Vol. 71, Núm. 8, pp. 1009-1016
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Sporadic hyperekplexia presenting with an ataxic gait
Journal of Clinical Neuroscience, Vol. 21, Núm. 2, pp. 345-346
2011
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Impact of psychiatric symptoms and sleep disorders on the quality of life of patients with Parkinson's disease
Journal of Neurology, Vol. 258, Núm. 3, pp. 494-499
2008
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Fluctuaciones motoras y discinesias en la enfermedad de Parkinson: Variables que discriminan ambas complicaciones en una muestra de 285 pacientes
Neurologia, Vol. 23, Núm. 8, pp. 494-498
2007
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Influence of motor symptoms upon the quality of life of patients with Parkinson's disease
European Neurology, Vol. 57, Núm. 3, pp. 161-165
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Restless legs syndrome in Parkinson's disease
Movement Disorders, Vol. 22, Núm. 13, pp. 1912-1916
2006
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Sleep complaints and their relation with drug treatment in patients suffering from Parkinson's disease
Movement Disorders, Vol. 21, Núm. 7, pp. 983-988
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Utilidad del estudio del sistema nervioso vegetativo en el diagnóstico diferencial entre la enfermedad de Parkinson y la atrofia multisistémica
Neurologia, Vol. 21, Núm. 3, pp. 119-123
2005
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A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease
Neurology, Vol. 64, Núm. 9, pp. 1578-1585
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Cerebrovascular disease in a tertiary care hospital. Current situation and issues to be improved
Revista de Neurologia, Vol. 40, Núm. 12, pp. 723-728
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Use of ziprasidonein parkinsonian patients with psychosis
Clinical Neuropharmacology, Vol. 28, Núm. 3, pp. 111-114
2003
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Leucoencefalopatía mitocondrial del lactante. ¿Forma precoz de un síndrome de Leigh?
Neurologia, Vol. 18, Núm. 5, pp. 241-247