Julio
Pardo Fernández
Complexo Hospitalario Universitario de Santiago
Santiago de Compostela, EspañaPublications in collaboration with researchers from Complexo Hospitalario Universitario de Santiago (36)
2024
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Electrodiagnostic subtyping in Guillain–Barré syndrome patients in the International Guillain–Barré Outcome Study
European Journal of Neurology, Vol. 31, Núm. 9
2023
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Characterizing SOD1 mutations in Spain: The impact of genotype, age and sex in the natural history of the disease
European Journal of Neurology, Vol. 30, Núm. 4, pp. 861-871
2022
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An International Perspective on Preceding Infections in Guillain-Barré Syndrome: The IGOS-1000 Cohort
Neurology, Vol. 99, Núm. 12, pp. E1299-E1313
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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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Electrodiagnosis of Guillain-Barre syndrome in the International GBS Outcome Study: Differences in methods and reference values
Clinical Neurophysiology, Vol. 138, pp. 231-240
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Predicting Outcome in Guillain-Barré Syndrome International Validation of the Modified Erasmus GBS Outcome Score
Neurology, Vol. 98, Núm. 5, pp. E518-E532
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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Thalamic atrophy in patients with pure hereditary spastic paraplegia type 4
Journal of Neurology, Vol. 268, Núm. 7, pp. 2429-2440
2020
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Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)
Cerebellum, Vol. 19, Núm. 4, pp. 501-509
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Clinical and neurophysiological response to ephedrine in a patient affected with slow-channel congenital myasthenic syndrome
Revista de Neurologia, Vol. 71, Núm. 6, pp. 221-224
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
2018
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Inflammatory myopathy in the context of an unusual overlapping laminopathy
Archives of Endocrinology and Metabolism, Vol. 62, Núm. 3, pp. 376-382
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Regional variation of Guillain-Barré syndrome
Brain, Vol. 141, Núm. 10, pp. 2866-2877
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The impact of rituximab infusion protocol on the long-term outcome in anti-MuSK myasthenia gravis
Annals of Clinical and Translational Neurology, Vol. 5, Núm. 6, pp. 710-716
2017
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Anti-NF155 chronic inflammatory demyelinating polyradiculoneuropathy strongly associates to HLA-DRB15
Journal of Neuroinflammation, Vol. 14, Núm. 1
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Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain
Scientific Reports, Vol. 7, Núm. 1
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PET and MRI detection of early and progressive neurodegeneration in spinocerebellar ataxia type 36
Movement Disorders, Vol. 32, Núm. 2, pp. 264-273
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Phenotypical features of a new dominant GDAP1 pathogenic variant (p.R226del) in axonal Charcot-Marie-Tooth disease
Neuromuscular Disorders, Vol. 27, Núm. 7, pp. 667-672