Fernando Isidro
Montón Álvarez
Investigador en el període 1990-2021
![Foto de Fernando Isidro](/img/nophoto.png)
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Hospital Universitario Nuestra Señora de Candelaria
Santa Cruz de Tenerife, EspañaPublicacions en col·laboració amb investigadors/es de Hospital Universitario Nuestra Señora de Candelaria (17)
2023
2022
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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
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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
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Longitudinal Study of Cognitive Functioning in Friedreich's Ataxia
Journal of the International Neuropsychological Society, Vol. 27, Núm. 4, pp. 343-350
2020
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Expanding the phenotypic and molecular spectrum of RNA polymerase III-related leukodystrophy
Neurology: Genetics, Vol. 6, Núm. 3
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Health-related quality of life and depressive symptoms in Friedreich ataxia
Quality of Life Research, Vol. 29, Núm. 2, pp. 413-420
2019
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Cognitive characterization of SCAR10 caused by a homozygous c.132dupA mutation in the ANO10 gene
Neurocase, Vol. 25, Núm. 5, pp. 195-201
2013
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Cognition in late-onset friedreich ataxia
Cerebellum, Vol. 12, Núm. 4, pp. 504-512
2012
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Cognition in friedreich ataxia
Cerebellum, Vol. 11, Núm. 4, pp. 834-844
2009
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Effectiveness and safety of treatments for degenerative ataxias: A systematic review
Movement Disorders, Vol. 24, Núm. 8, pp. 1111-1124
2008
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Lack of association of endothelial nitric oxide synthase polymorphisms and migraine
Headache, Vol. 48, Núm. 7, pp. 1115-1119
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SUNCT and trigeminal neuralgia attributed to meningoencephalitis
Journal of Headache and Pain, Vol. 9, Núm. 1, pp. 51-53
2007
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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
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The value of diffusion-weighted MRI in the diagnosis of cerebral fat embolism
Journal of Neuroimaging, Vol. 17, Núm. 1, pp. 78-80
1996
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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
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Axonal form of Guillain–Barré syndrome: Evidence for macrophage‐associated demyelination
Muscle & Nerve, Vol. 16, Núm. 7, pp. 744-751
1991
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Reversible Schwann cell hypertrophy in lead neuropathy
Neuropathology and Applied Neurobiology, Vol. 17, Núm. 3, pp. 231-236