Publications en collaboration avec des chercheurs de Hospital Universitario Nuestra Señora de Candelaria (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