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Page 1
Orthopedic Conditions and Interplay with Functional Abilities and MECP2 Variant Subtype in Rett Syndrome Patients.
Galán-Olleros M, González-Alguacil E, Soto-Insuga V, Vara-Arias MT, Ortiz-Cabrera NV, Serrano JI, Egea-Gámez RM, García-Peñas JJ, Martínez-Caballero I; RTT-HNJ, Rett Syndrome Multidisciplinary Group of Hospital Infantil Universitario Niño Jesús. Galán-Olleros M, et al. Among authors: soto insuga v. J Autism Dev Disord. 2024 May 25. doi: 10.1007/s10803-024-06399-y. Online ahead of print. J Autism Dev Disord. 2024. PMID: 38795288
Frequency, symptoms, risk factors, and outcomes of autoimmune encephalitis after herpes simplex encephalitis: a prospective observational study and retrospective analysis.
Armangue T, Spatola M, Vlagea A, Mattozzi S, Cárceles-Cordon M, Martinez-Heras E, Llufriu S, Muchart J, Erro ME, Abraira L, Moris G, Monros-Giménez L, Corral-Corral Í, Montejo C, Toledo M, Bataller L, Secondi G, Ariño H, Martínez-Hernández E, Juan M, Marcos MA, Alsina L, Saiz A, Rosenfeld MR, Graus F, Dalmau J; Spanish Herpes Simplex Encephalitis Study Group. Armangue T, et al. Lancet Neurol. 2018 Sep;17(9):760-772. doi: 10.1016/S1474-4422(18)30244-8. Epub 2018 Jul 23. Lancet Neurol. 2018. PMID: 30049614 Free PMC article.
[Insomnia in children and adolescents. A consensus document].
Pin Arboledas G, Soto Insuga V, Jurado Luque MJ, Fernandez Gomariz C, Hidalgo Vicario I, Lluch Rosello A, Rodríguez Hernández PJ, Madrid JA. Pin Arboledas G, et al. An Pediatr (Barc). 2017 Mar;86(3):165.e1-165.e11. doi: 10.1016/j.anpedi.2016.06.005. Epub 2016 Jul 28. An Pediatr (Barc). 2017. PMID: 27476002 Free article. Spanish.
Neuropsychiatric manifestations of Graves' disease in paediatric patients.
Losada-Del Pozo R, Soto-Insuga V, Martínez González M, Soriano Guillén L. Losada-Del Pozo R, et al. Neurologia. 2017 Apr;32(3):196-197. doi: 10.1016/j.nrl.2015.05.001. Epub 2015 Jun 19. Neurologia. 2017. PMID: 26096670 Free article. English, Spanish. No abstract available.
[The importance of sleep problems in children with headache and other neurodevelopmental disorders in neuropaediatric services].
Perez-Villena A, Soto-Insuga V, Castaño-De la Mota C, Martin-Del Valle F, Pons-Rodriguez M, Losada-Del Pozo R, Moreno-Acero N, Alarcon-Martinez H, Rodrigo-Moreno M, Miravet-Fuster E, Monfort-Belenguer L, Polo-Antunez A, Martinez-Bermejo A, Merino-Andreu M. Perez-Villena A, et al. Rev Neurol. 2016 Jan 16;62(2):61-7. Rev Neurol. 2016. PMID: 26758352 Free article. Spanish.
Glut1 deficiency is a rare but treatable cause of childhood absence epilepsy with atypical features.
Soto-Insuga V, López RG, Losada-Del Pozo R, Rodrigo-Moreno M, Cayuelas EM, Giráldez BG, Díaz-Gómez E, Sánchez-Martín G, García LO, Serratosa JM; Grupo Español de Genética de las Epilepsias de la Infancia (GEGEI). Soto-Insuga V, et al. Epilepsy Res. 2019 Aug;154:39-41. doi: 10.1016/j.eplepsyres.2019.04.003. Epub 2019 Apr 21. Epilepsy Res. 2019. PMID: 31035243
47 results