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dc.contributor | Universitat de Barcelona |
---|---|
dc.contributor.author | Panagiotakaki, Eleni |
dc.contributor.author | Grandis, Elisa de |
dc.contributor.author | Stagnaro, Michela |
dc.contributor.author | Heinzen, Erin L. |
dc.contributor.author | Fons, Carmen |
dc.contributor.author | Sisodiya, Sanjay |
dc.contributor.author | Vries, Boukje de |
dc.contributor.author | Goubau, Christophe |
dc.contributor.author | Weckhuysen, Sarah |
dc.contributor.author | Kemlink, David |
dc.contributor.author | Scheffer, Ingrid |
dc.contributor.author | Lesca, Gaëtan |
dc.contributor.author | Rabilloud, Muriel |
dc.contributor.author | Klich, Amna |
dc.contributor.author | Ramirez-Camacho, Alia |
dc.contributor.author | Ulate-Campos, Adriana |
dc.contributor.author | Campistol Plana, Jaume |
dc.contributor.author | Giannotta, Melania |
dc.contributor.author | Moutard, Marie L. |
dc.contributor.author | Doummar, Diane |
dc.contributor.author | Hubsch-Bonneaud, Cecile |
dc.contributor.author | Jaffer, Fatima |
dc.contributor.author | Cross, Helen |
dc.contributor.author | Gurrieri, Fiorella |
dc.contributor.author | Tiziano, Danilo |
dc.contributor.author | Nevsimalova, Sona |
dc.contributor.author | Nicole, Sophie |
dc.contributor.author | Neville, Brian |
dc.contributor.author | Maagdenberg, Arn M.J.M. van den |
dc.contributor.author | Mikati, Mohamad |
dc.contributor.author | Goldstein, David B. |
dc.contributor.author | Vavassori, Rosaria |
dc.contributor.author | Arzimanoglou, Alexis |
dc.contributor.author | Italian IBAHC Consortium |
dc.contributor.author | French AHC Consortium |
dc.contributor.author | International AHC Consortium |
dc.date | 2017-06-06T14:40:16Z |
dc.date | 2017-06-06T14:40:16Z |
dc.date | 2015-09-26 |
dc.date | 2017-06-06T14:40:16Z |
dc.identifier.citation | 1750-1172 |
dc.identifier.citation | 667569 |
dc.identifier.uri | http://hdl.handle.net/2445/112025 |
dc.format | 13 p. |
dc.format | application/pdf |
dc.language.iso | eng |
dc.publisher | BioMed Central |
dc.relation | Reproducció del document publicat a: https://doi.org/10.1186/s13023-015-0335-5 |
dc.relation | Orphanet Journal of Rare Diseases, 2015, vol. 10, num. 123 |
dc.relation | https://doi.org/10.1186/s13023-015-0335-5 |
dc.rights | cc-by (c) Panagiotakaki, Eleni et al., 2015 |
dc.rights | info:eu-repo/semantics/openAccess |
dc.rights | http://creativecommons.org/licenses/by/3.0/es |
dc.subject | Hemiplègia |
dc.subject | Genètica mèdica |
dc.subject | Mutació (Biologia) |
dc.subject | Hemiplegia |
dc.subject | Medical genetics |
dc.subject | Mutation (Biology) |
dc.title | Clinical profile of patients with ATP1A3 mutations in alternating hemiplegia of childhood-a study of 155 patients. |
dc.type | info:eu-repo/semantics/article |
dc.type | info:eu-repo/semantics/publishedVersion |
dc.description.abstract |