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Revista De Neurologia|January 27, 2022
[Validation of the Spanish version of the Charcot-Marie-Tooth disease Pediatric Scale (CMTPedS)]I Pitarch-Castellano, H Argente-Escrig, M Frasquet, et al.
Clinical Genetics|May 2, 2007
The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4R Claramunt, T Sevilla, V Lupo, et al.
Neurologia|April 10, 2026
Myasthenia gravis in Spain: A survey of specialized neurologists to uncover unmet needsE Cortés-Vicente, C Casasnovas, R Juntas, et al.
Revista De Neurologia|July 31, 2007
[Migraine with aura, right-to-left shunt and frequency of seizures]J I Tembl-Ferrairó, A Lago-Martín, T Sevilla, et al.
Neurologia|September 19, 2021
Analysis of the diagnostic pathway and delay in patients with amyotrophic lateral sclerosis in the Valencian CommunityJ F Vázquez-Costa, M Martínez-Molina, M Fernández-Polo, et al.
Clinical Genetics|September 18, 2012
Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depthT Sevilla, D Martínez-Rubio, C Márquez, et al.
Transplantation Proceedings|January 3, 2006
Incidence of and risk factors for neurologic complications after heart transplantationF Pérez-Miralles, J C Sánchez-Manso, L Almenar-Bonet, et al.
Neurologia (Barcelona, Spain)|June 28, 2011
[Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease]J Berciano, T Sevilla, C Casasnovas, et al.
European Journal of Neurology|September 8, 2020
Bi-allelic mutations in EGR2 cause autosomal recessive demyelinating neuropathy by disrupting the EGR2-NAB complexV Lupo, S Won, M Frasquet, et al.
Human Molecular Genetics|December 1, 1993
Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesisF Palau, A Löfgren, P De Jonghe, et al.
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