Julio
Pardo Fernández
Universitat de València
Valencia, EspañaPublicacións en colaboración con investigadores/as de Universitat de València (5)
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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Drug-refractory myasthenia gravis: Clinical characteristics, treatments, and outcome
Annals of Clinical and Translational Neurology, Vol. 9, Núm. 2, pp. 122-131
2018
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Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying MME mutations
Journal of Medical Genetics, Vol. 55, Núm. 12, pp. 814-823
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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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Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain
Scientific Reports, Vol. 7, Núm. 1