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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. Among authors: arrabal fernandez l. 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.
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. Among authors: arrabal fernandez l. Neurologia (Engl Ed). 2020 Jul 8:S0213-4853(20)30137-7. doi: 10.1016/j.nrl.2020.04.025. Online ahead of print. Neurologia (Engl Ed). 2020. PMID: 32653103 Free article. English, Spanish.
Dilated Cardiomyopathy With Short QT Interval Suggests Primary Carnitine Deficiency.
Perin F, Rodríguez-Vázquez Del Rey MDM, Carreras-Blesa C, Arrabal-Fernández L, Jiménez-Jáimez J, Tercedor L. Perin F, et al. Among authors: arrabal fernandez l. Rev Esp Cardiol (Engl Ed). 2018 Dec;71(12):1074-1075. doi: 10.1016/j.rec.2017.09.004. Epub 2017 Dec 2. Rev Esp Cardiol (Engl Ed). 2018. PMID: 29198778 English, Spanish. No abstract available.
Severe congenital X-linked myopathy with excessive autophagy secondary to an apparently synonymous but pathogenic novel variant.
Blanco-Arias P, Medina Martínez I, Arrabal Fernández L, Rivas Infante E, Salmerón Fernández MJ, González Hervás C, Azcón González de Aguilar P, Armengol L, Pedrinaci S, Perin F. Blanco-Arias P, et al. Among authors: arrabal fernandez l. Neuromuscul Disord. 2023 Jul;33(7):557-561. doi: 10.1016/j.nmd.2023.05.008. Epub 2023 May 23. Neuromuscul Disord. 2023. PMID: 37329680
[Combined treatment with antiepileptic drugs. Andalusian Epilepsy Guide 2015].
Sánchez-Álvarez JC, Ramos-Lizana J, Machado-Casas IS, Serrano-Castro PJ, Martínez-Antón JL, Ruiz-Giménez J; Comité Editorial de la Guía de Epilepsia de la Sociedad Andaluza de Epilepsia 2015. Sánchez-Álvarez JC, et al. Rev Neurol. 2015 Apr 16;60(8):365-79. Rev Neurol. 2015. PMID: 25857861 Free article. Spanish.
Sepiapterin reductase deficiency: a treatable mimic of cerebral palsy.
Friedman J, Roze E, Abdenur JE, Chang R, Gasperini S, Saletti V, Wali GM, Eiroa H, Neville B, Felice A, Parascandalo R, Zafeiriou DI, Arrabal-Fernandez L, Dill P, Eichler FS, Echenne B, Gutierrez-Solana LG, Hoffmann GF, Hyland K, Kusmierska K, Tijssen MA, Lutz T, Mazzuca M, Penzien J, Poll-The BT, Sykut-Cegielska J, Szymanska K, Thöny B, Blau N. Friedman J, et al. Among authors: arrabal fernandez l. Ann Neurol. 2012 Apr;71(4):520-30. doi: 10.1002/ana.22685. Ann Neurol. 2012. PMID: 22522443