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The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome S Vidal, N Brandi, P Pacheco, E Gerotina, L Blasco, JR Trotta, S Derdak, ... Scientific reports 7 (1), 12288, 2017 | 31 | 2017 |
Vanishing white matter disease in a spanish population E Turón-Viñas, M Pineda, V Cusí, E López-Laso, RL Del Pozo, ... Journal of central nervous system disease 6, JCNSD. S13540, 2014 | 30 | 2014 |
Haematopoietic stem cell transplantation for mucopolysaccharidosis type VII: a case report L Sisinni, M Pineda, MJ Coll, L Gort, E Turon, M Torrent, A Ey, E Tobajas, ... Pediatric transplantation 22 (7), e13278, 2018 | 19 | 2018 |
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Eculizumab in a child with atypical haemolytic uraemic syndrome and haemophagocytic lymphohistiocytosis triggered by cytomegalovirus infection GM Fraga-Rodriguez, S Brió-Sanagustin, E Turón-Viñas, BP Dixon, ... Case Reports 2017, bcr-2016-219065, 2017 | 9 | 2017 |
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Long-term efficacy of perampanel in a child with Dravet syndrome E Turón-Viñas, A Díaz-Gómez, E Coca, L Dougherty, C Ruiz, S Boronat Child Neurology Open 8, 2329048X211050711, 2021 | 4 | 2021 |
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