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Prevalencia de los trastornos del espectro autista en niños en Estados Unidos, Europa y España: coincidencias y discrepancias I Málaga, R Blanco Lago, A Hedrera-Fernández, N Álvarez-Álvarez, ... Medicina (Buenos Aires) 79 (1), 4-9, 2019 | 71 | 2019 |
Prevalence of autism spectrum disorders in USA, Europe and Spain: Coincidences and discrepancies I Malaga, R Blanco-Lago, A Hedrera-Fernandez, N Alvarez-Alvarez, ... Medicina 79 (Suppl 1), 4-9, 2019 | 21 | 2019 |
Diagnosis of genetic white matter disorders by singleton whole-exome and genome sequencing using interactome-driven prioritization A Schlüter, A Rodríguez-Palmero, E Verdura, V Vélez-Santamaría, M Ruiz, ... Neurology 98 (9), e912-e923, 2022 | 19 | 2022 |
An unusual presentation of paediatric Listeria meningitis with selective spinal grey matter involvement and acute demyelinating polyneuropathy A Papandreou, A Hedrera-Fernandez, M Kaliakatsos, WK Chong, S Bhate european journal of paediatric neurology 20 (1), 196-199, 2016 | 17 | 2016 |
Paradigmatic De Novo GRIN1 Variants Recapitulate Pathophysiological Mechanisms Underlying GRIN1-Related Disorder Clinical Spectrum A Santos-Gómez, F Miguez-Cabello, N Juliá-Palacios, D García-Navas, ... International Journal of Molecular Sciences 22 (23), 12656, 2021 | 7 | 2021 |
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Outbreak of enterovirus infection with neurological presentations in a pediatric population in Northern Spain: a clinical observational study A Hedrera-Fernandez, R Cancho-Candela, M Arribas-Arceredillo, ... Neuropediatrics 52 (03), 192-200, 2021 | 4 | 2021 |
Opsoclonus-myoclonus syndrome: clinical characteristics, therapeutic considerations, and prognostic factors in a Spanish paediatric cohort V Cantarín-Extremera, M Jiménez-Legido, S Aguilera-Albesa, ... Neurología (English Edition) 38 (2), 93-105, 2023 | 3 | 2023 |
Epilepsia sintomática con inicio que imita el síndrome de Panayiotopoulos: importancia de la neuroimagen VA Oreña-Ansorena, R Blanco-Lago, A Hedrera-Fernández, M Bonifacio, ... Rev. neurol.(Ed. impr.), 134-138, 2020 | 3 | 2020 |
Síndrome de Kleine-Levin: diagnóstico diferencial en los síndromes encefalíticos recurrentes del adolescente A Duat-Rodríguez, I Martínez-Albaladejo, I Pérez-Sebastián, ... Rev. neurol.(Ed. impr.), 313-318, 2017 | 3 | 2017 |
Genome sequencing and comprehensive rare-variant analysis of 465 families with neurodevelopmental disorders A Sanchis-Juan, K Megy, J Stephens, CA Ricaurte, E Dewhurst, K Low, ... The American Journal of Human Genetics 110 (8), 1343-1355, 2023 | 2 | 2023 |
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Benign spasms of infancy or benign myoclonus of early infancy: polygraph-EEG recordings NÁ Álvarez, RP de la Vega, MAG Trueba, LS González, AG Acero, ... Epileptic Disorders 23 (5), 801-802, 2021 | 2 | 2021 |
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Expanding the phenotypic spectrum of TRAPPC11-related muscular dystrophy: 25 Roma individuals carrying a founder variant M Justel, C Jou, A Sariego-Jamardo, NA Juliá-Palacios, C Ortez, ML Poch, ... Journal of medical genetics 60 (10), 965-973, 2023 | 1 | 2023 |
Clinical features of the outbreak of Enterovirus infection with neurological impairment in children in the North of Spain AH Fernandez, DC Moreno, AS Jamardo, CR Fernandez, MEM Ruiz, ... European Journal of Paediatric Neurology 21, e89, 2017 | 1 | 2017 |
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