Teresa Sevilla
Universitat de València(ES)Hospital Universitari i Politècnic La Fe(ES)Centre for Biomedical Network Research on Rare Diseases(ES)Centro de Investigación Biomédica en Red(ES)ERN GUARD-Heart(NL)Instituto de Investigación Sanitaria La Fe(ES)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases, Neurogenetic and Muscular Disorders Research, Botulinum Toxin and Related Neurological Disorders, Amyotrophic Lateral Sclerosis Research
Most-Cited Works
- → The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease(2001)359 cited
- → Clinical and therapeutic features of myasthenia gravis in adults based on age at onset(2020)162 cited
- → Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies(1997)137 cited
- → Charcot-Marie-Tooth disease(2013)129 cited
- → Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis(1993)128 cited
- → REVERSIBLE PARANEOPLASTIC LIMBIC ENCEPHALITIS ASSOCIATED WITH ANTIBODIES TO THE AMPA RECEPTOR(2010)127 cited