| Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study T Armangue, G Olivé-Cirera, E Martínez-Hernandez, M Sepulveda, ... The Lancet Neurology 19 (3), 234-246, 2020 | 250 | 2020 |
| Parálisis cerebral: concepto y registros de base poblacional A Camacho-Salas, CR Pallás-Alonso, J De La Cruz-Bértolo, ... Rev Neurol 45 (8), 503-8, 2007 | 164 | 2007 |
| Epilepsy in tuberous sclerosis complex: findings from the TOSCA Study R Nabbout, E Belousova, MP Benedik, T Carter, V Cottin, P Curatolo, ... Epilepsia open 4 (1), 73-84, 2019 | 163 | 2019 |
| Cholinergic–dopaminergic imbalance in Pisa syndrome A Villarejo, A Camacho, R García–Ramos, T Moreno, M Penas, R Juntas, ... Clinical neuropharmacology 26 (3), 119-121, 2003 | 131 | 2003 |
| Congenital titinopathy: comprehensive characterization and pathogenic insights EC Oates, KJ Jones, S Donkervoort, A Charlton, S Brammah, JE Smith III, ... Annals of neurology 83 (6), 1105-1124, 2018 | 109 | 2018 |
| Cognitive and behavioral profile in females with epilepsy with PDCH19 mutation: two novel mutations and review of the literature A Camacho, R Simón, R Sanz, A Viñuela, A Martínez-Salio, F Mateos Epilepsy & Behavior 24 (1), 134-137, 2012 | 59 | 2012 |
| New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy J Alonso-Perez, L González-Quereda, L Bello, M Guglieri, V Straub, ... Brain 143 (9), 2696-2708, 2020 | 54 | 2020 |
| Spontaneous carotid and vertebral artery dissection in children A Camacho, A Villarejo, AM de Aragón, R Simón, F Mateos Pediatric neurology 25 (3), 250-253, 2001 | 54 | 2001 |
| Consensus on the diagnosis, treatment and follow-up of patients with Duchenne muscular dystrophy AN Osorio, JM Cantillo, AC Salas, MM Garrido, JJV Padilla Neurología (English Edition) 34 (7), 469-481, 2019 | 53 | 2019 |
| Mirrored-self misidentification in a patient without dementia: evidence for right hemispheric and bifrontal damage A Villarejo, VP Martin, T Moreno-Ramos, A Camacho-Salas, ... Neurocase 17 (3), 276-284, 2011 | 50 | 2011 |
| Olanzapine-induced myoclonic status A Camacho, M García-Navarro, B Martínez, A Villarejo, E Pomares Clinical neuropharmacology 28 (3), 145-147, 2005 | 50 | 2005 |
| Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti–Boltshauser syndrome) A Micalizzi, A Poretti, M Romani, M Ginevrino, T Mazza, C Aiello, G Zanni, ... European Journal of Human Genetics 24 (9), 1262-1267, 2016 | 44 | 2016 |
| New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy E Martín-Hernández, ME Rodríguez-García, A Camacho, ... Neurogenetics 17, 259-263, 2016 | 40 | 2016 |
| Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert GG Gutiérrez, J Díaz-Manera, M Almendrote, S Azriel, JE Bárcena, ... Medicina Clínica 153 (2), 82. e1-82. e17, 2019 | 37 | 2019 |
| Distrofia muscular de Duchenne AC Salas Anales de Pediatría Continuada 12 (2), 47-54, 2014 | 37 | 2014 |
| Parálisis cerebral infantil: importancia de los registros poblacionales A Camacho-Salas Rev. neurol.(Ed. impr.), 15-20, 2008 | 37 | 2008 |
| Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease GG Gutiérrez, J Díaz-Manera, M Almendrote, S Azriel, JE Bárcena, ... Medicina Clínica (English Edition) 153 (2), 82. e1-82. e17, 2019 | 36 | 2019 |
| Distribution and genotype-phenotype correlation of GDAP1 mutations in Spain R Sivera, M Frasquet, V Lupo, T García-Sobrino, P Blanco-Arias, J Pardo, ... Scientific reports 7 (1), 6677, 2017 | 35 | 2017 |
| A newly distal hereditary motor neuropathy caused by a rare AIFM1 mutation P Sancho, A Sánchez-Monteagudo, A Collado, C Marco-Marín, ... Neurogenetics 18, 245-250, 2017 | 34 | 2017 |
| Consenso para el diagnóstico, tratamiento y seguimiento del paciente con distrofia muscular de Duchenne AN Osorio, JM Cantillo, AC Salas, MM Garrido, JJV Padilla Neurología 34 (7), 469-481, 2019 | 32 | 2019 |
