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142 results

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Page 1
Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: phenotypic homogeneity due to the homozygous c.125C>T mutation in ASAH1.
Giráldez BG, Guerrero-López R, Ortega-Moreno L, Verdú A, Carrascosa-Romero MC, García-Campos Ó, García-Muñozguren S, Pardal-Fernández JM, Serratosa JM. Giráldez BG, et al. Among authors: serratosa jm. Neuromuscul Disord. 2015 Mar;25(3):222-4. doi: 10.1016/j.nmd.2014.11.007. Epub 2014 Nov 22. Neuromuscul Disord. 2015. PMID: 25578555
Hyperexcitability and epileptic seizures in a model of frontotemporal dementia.
García-Cabrero AM, Guerrero-López R, Giráldez BG, Llorens-Martín M, Avila J, Serratosa JM, Sánchez MP. García-Cabrero AM, et al. Among authors: serratosa jm. Neurobiol Dis. 2013 Oct;58:200-8. doi: 10.1016/j.nbd.2013.06.005. Epub 2013 Jun 14. Neurobiol Dis. 2013. PMID: 23774255
Long-term safety and efficacy of eslicarbazepine acetate in patients with focal seizures: results of the 1-year ESLIBASE retrospective study.
Villanueva V, Serratosa JM, Guillamón E, Garcés M, Giráldez BG, Toledo M, Salas-Puig J, López González FJ, Flores J, Rodríguez-Uranga J, Castillo A, Mauri JA, Camacho JL, López-Gomáriz E, Giner P, Torres N, Palau J, Molins A. Villanueva V, et al. Among authors: serratosa jm. Epilepsy Res. 2014 Sep;108(7):1243-52. doi: 10.1016/j.eplepsyres.2014.04.014. Epub 2014 May 14. Epilepsy Res. 2014. PMID: 24908564
Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene.
Guerrero-López R, Ortega-Moreno L, Giráldez BG, Alarcón-Morcillo C, Sánchez-Martín G, Nieto-Barrera M, Gutiérrez-Delicado E, Gómez-Garre P, Martínez-Bermejo A, García-Peñas JJ, Serratosa JM. Guerrero-López R, et al. Among authors: serratosa jm. Epilepsy Res. 2014 Oct;108(8):1274-8. doi: 10.1016/j.eplepsyres.2014.06.011. Epub 2014 Jul 7. Epilepsy Res. 2014. PMID: 25060993
Mild Lafora disease: clinical, neurophysiologic, and genetic findings.
Ferlazzo E, Canafoglia L, Michelucci R, Gambardella A, Gennaro E, Pasini E, Riguzzi P, Plasmati R, Volpi L, Labate A, Gasparini S, Villani F, Casazza M, Viri M, Zara F, Minassian BA, Turnbull J, Serratosa JM, Guerrero-López R, Franceschetti S, Aguglia U. Ferlazzo E, et al. Among authors: serratosa jm. Epilepsia. 2014 Dec;55(12):e129-33. doi: 10.1111/epi.12806. Epub 2014 Sep 30. Epilepsia. 2014. PMID: 25270369 Free article.
Novel mutation in STXBP1 gene in a patient with non-lesional Ohtahara syndrome.
Ortega-Moreno L, Giráldez BG, Verdú A, García-Campos O, Sánchez-Martín G, Serratosa JM, Guerrero-López R. Ortega-Moreno L, et al. Among authors: serratosa jm. Neurologia. 2016 Oct;31(8):523-7. doi: 10.1016/j.nrl.2014.10.017. Epub 2015 Jan 24. Neurologia. 2016. PMID: 25631041 Free article. English, Spanish.
142 results