Hospital Universitario Nuestra Señora de Candelaria -ko ikertzaileekin lankidetzan egindako argitalpenak (17)

2023

  1. Quality of life and mental health in young strokes

    Neurologia

2022

  1. Clinical and genetic features of a large homogeneous cohort of oculopharyngeal muscular dystrophy patients from the Canary Islands

    European Journal of Neurology, Vol. 29, Núm. 5, pp. 1488-1495

2021

  1. Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C

    Journal of Clinical Endocrinology and Metabolism, Vol. 106, Núm. 2, pp. E660-E674

  2. Longitudinal Study of Cognitive Functioning in Friedreich's Ataxia

    Journal of the International Neuropsychological Society, Vol. 27, Núm. 4, pp. 343-350

2020

  1. Expanding the phenotypic and molecular spectrum of RNA polymerase III-related leukodystrophy

    Neurology: Genetics, Vol. 6, Núm. 3

  2. Health-related quality of life and depressive symptoms in Friedreich ataxia

    Quality of Life Research, Vol. 29, Núm. 2, pp. 413-420

2019

  1. Cognitive characterization of SCAR10 caused by a homozygous c.132dupA mutation in the ANO10 gene

    Neurocase, Vol. 25, Núm. 5, pp. 195-201

2013

  1. Cognition in late-onset friedreich ataxia

    Cerebellum, Vol. 12, Núm. 4, pp. 504-512

2012

  1. Cognition in friedreich ataxia

    Cerebellum, Vol. 11, Núm. 4, pp. 834-844

2009

  1. Effectiveness and safety of treatments for degenerative ataxias: A systematic review

    Movement Disorders, Vol. 24, Núm. 8, pp. 1111-1124

2008

  1. Lack of association of endothelial nitric oxide synthase polymorphisms and migraine

    Headache, Vol. 48, Núm. 7, pp. 1115-1119

  2. SUNCT and trigeminal neuralgia attributed to meningoencephalitis

    Journal of Headache and Pain, Vol. 9, Núm. 1, pp. 51-53

2007

  1. Genetic association study and meta-analysis of the HTR2C Cys23Ser polymorphism and migraine

    Journal of Headache and Pain, Vol. 8, Núm. 4, pp. 231-235

  2. The value of diffusion-weighted MRI in the diagnosis of cerebral fat embolism

    Journal of Neuroimaging, Vol. 17, Núm. 1, pp. 78-80

1996

  1. Arginine-164-tryptophan substitution in connexin32 associated with X linked dominant Charcot-Marie-Tooth disease

    Journal of Medical Genetics, Vol. 33, Núm. 5, pp. 413-415

1993

  1. Axonal form of Guillain–Barré syndrome: Evidence for macrophage‐associated demyelination

    Muscle & Nerve, Vol. 16, Núm. 7, pp. 744-751

1991

  1. Reversible Schwann cell hypertrophy in lead neuropathy

    Neuropathology and Applied Neurobiology, Vol. 17, Núm. 3, pp. 231-236