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Opsoclonus-myoclonus syndrome: Clinical characteristics, therapeutic considerations, and prognostic factors in a Spanish paediatric cohort.
Cantarín-Extremera V, Jiménez-Legido M, Aguilera-Albesa S, Hedrera-Fernández A, Arrabal-Fernández L, Gorría-Redondo N, Martí-Carrera I, Yoldi-Pedtri ME, Sagaseta-De Ilúrdoz M, González-Gutiérrez-Solana L. Cantarín-Extremera V, et al. Neurologia (Engl Ed). 2023 Mar;38(2):93-105. doi: 10.1016/j.nrleng.2020.04.030. Epub 2022 Nov 15. Neurologia (Engl Ed). 2023. PMID: 36396095 Free article.
[Von Hippel-Lindau disease in a patient with l-2-hydroxyglutaric aciduria].
Duat Rodríguez A, Ruiz-Falcó Rojas ML, González Gutiérrez-Solana L, Cantarín Extremera V, Pedrón Giner C. Duat Rodríguez A, et al. An Pediatr (Barc). 2012 Jul;77(1):63-4. doi: 10.1016/j.anpedi.2012.02.006. Epub 2012 Apr 4. An Pediatr (Barc). 2012. PMID: 22481001 Free article. Spanish. No abstract available.
Immune-mediated mechanisms in the pathogenesis of Hopkins syndrome.
Cantarín-Extremera V, González-Gutiérrez-Solana L, Ramírez-Orellana M, López-Marín L, Duat-Rodríguez A, Ruíz-Falcó-Rojas ML. Cantarín-Extremera V, et al. Pediatr Neurol. 2012 Nov;47(5):373-4. doi: 10.1016/j.pediatrneurol.2012.08.006. Pediatr Neurol. 2012. PMID: 23044022
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.
Study of paediatric patients with the clinical and biochemical phenotype of glucose transporter type 1 deficiency syndrome.
Jiménez Legido M, Cortés Ledesma C, Bernardino Cuesta B, López Marín L, Cantarín Extremera V, Pérez-Cerdá C, Pérez González B, López Martín E, González Gutiérrez-Solana L. Jiménez Legido M, et al. Neurologia (Engl Ed). 2022 Mar;37(2):91-100. doi: 10.1016/j.nrl.2018.10.006. Epub 2019 Apr 29. Neurologia (Engl Ed). 2022. PMID: 31047728 Free article. English, Spanish.
53 results