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Diagnosis of epilepsy over the course of the disease.
Saiz Díaz RA, Martínez Bermejo A, Gómez Alonso J. Saiz Díaz RA, et al. Among authors: martinez bermejo a. Neurologist. 2007 Nov;13(6 Suppl 1):S11-9. doi: 10.1097/NRL.0b013e31815bb146. Neurologist. 2007. PMID: 18090946 Review.
[Diagnosis in severe myoclonic epilepsy in childhood: study of 13 cases].
Fernández-Jaén A, León MC, Martínez-Granero MA, Martínez-Bermejo A, López-Martín V, Pascual-Castroviejo I. Fernández-Jaén A, et al. Among authors: martinez granero ma, martinez bermejo a. Rev Neurol. 1998 May;26(153):759-62. Rev Neurol. 1998. PMID: 9634662 Spanish.
[Benign myoclonic epilepsy -a curious case report].
Salgueiro AB, Velázquez-Fragua R, Martínez-Bermejo A. Salgueiro AB, et al. Among authors: martinez bermejo a. Rev Neurol. 2007 Aug 1-15;45(3):152-4. Rev Neurol. 2007. PMID: 17661274 Free article. Spanish.
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: martinez bermejo a. 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
Hypomelanosis of ITO. A study of 76 infantile cases.
Pascual-Castroviejo I, Roche C, Martinez-Bermejo A, Arcas J, Lopez-Martin V, Tendero A, Esquiroz JL, Pascual-Pascual SI. Pascual-Castroviejo I, et al. Among authors: martinez bermejo a. Brain Dev. 1998 Jan;20(1):36-43. doi: 10.1016/s0387-7604(97)00097-1. Brain Dev. 1998. PMID: 9533559
98 results