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Miller Fisher syndrome and polyneuritis cranialis in COVID-19.
Gutiérrez-Ortiz C, Méndez-Guerrero A, Rodrigo-Rey S, San Pedro-Murillo E, Bermejo-Guerrero L, Gordo-Mañas R, de Aragón-Gómez F, Benito-León J. Gutiérrez-Ortiz C, et al. Neurology. 2020 Aug 4;95(5):e601-e605. doi: 10.1212/WNL.0000000000009619. Epub 2020 Apr 17. Neurology. 2020. PMID: 32303650
Generalized myoclonus in COVID-19.
Rábano-Suárez P, Bermejo-Guerrero L, Méndez-Guerrero A, Parra-Serrano J, Toledo-Alfocea D, Sánchez-Tejerina D, Santos-Fernández T, Folgueira-López MD, Gutiérrez-Gutiérrez J, Ayuso-García B, González de la Aleja J, Benito-León J. Rábano-Suárez P, et al. Neurology. 2020 Aug 11;95(6):e767-e772. doi: 10.1212/WNL.0000000000009829. Epub 2020 May 21. Neurology. 2020. PMID: 32439821 Free PMC article.
Persistent asymptomatic or mild symptomatic hyperCKemia due to mutations in ANO5: the mildest end of the anoctaminopathies spectrum.
Panadés-de Oliveira L, Bermejo-Guerrero L, de Fuenmayor-Fernández de la Hoz CP, Cantero Montenegro D, Hernández Lain A, Martí P, Muelas N, Vilchez JJ, Domínguez-González C. Panadés-de Oliveira L, et al. J Neurol. 2020 Sep;267(9):2546-2555. doi: 10.1007/s00415-020-09872-7. Epub 2020 May 4. J Neurol. 2020. PMID: 32367299
Plasmapheresis in the Treatment of Refractory Myoclonic Status. A Case Report.
Gutierrez-Gutierrez J, Muñoz-Calahorro R, Bermejo-Guerrero L, Molina-Collado Z, de la Fuente IS, Sánchez-Izquierdo JA. Gutierrez-Gutierrez J, et al. Among authors: bermejo guerrero l. J Crit Care Med (Targu Mures). 2021 Nov 6;7(4):290-293. doi: 10.2478/jccm-2021-0041. eCollection 2021 Oct. J Crit Care Med (Targu Mures). 2021. PMID: 34934819 Free PMC article.
Distal hereditary motor neuronopathy as a new phenotype associated with variants in BAG3.
de Fuenmayor-Fernández de la Hoz CP, Lupo V, Bermejo-Guerrero L, Martín-Jiménez P, Hernández-Laín A, Olivé M, Gallardo E, Esteban-Pérez J, Espinós C, Domínguez-González C. de Fuenmayor-Fernández de la Hoz CP, et al. Among authors: bermejo guerrero l. J Neurol. 2024 Feb;271(2):986-994. doi: 10.1007/s00415-023-12039-9. Epub 2023 Oct 31. J Neurol. 2024. PMID: 37907725
Clinical, Histological, and Genetic Features of 25 Patients with Autosomal Dominant Progressive External Ophthalmoplegia (ad-PEO)/PEO-Plus Due to TWNK Mutations.
Bermejo-Guerrero L, de Fuenmayor-Fernández de la Hoz CP, Serrano-Lorenzo P, Blázquez-Encinar A, Gutiérrez-Gutiérrez G, Martínez-Vicente L, Galán-Dávila L, García-García J, Arenas J, Muelas N, Hernández-Laín A, Domínguez-González C, Martín MA. Bermejo-Guerrero L, et al. J Clin Med. 2021 Dec 22;11(1):22. doi: 10.3390/jcm11010022. J Clin Med. 2021. PMID: 35011763 Free PMC article.
16 results