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Mitochondrion|April 10, 2024
Remarkable clinical improvement with oral nucleoside treatment in a patient with adult-onset TK2 deficiency: A case reportLaura Bermejo-Guerrero, Ana Hernández-Voth, Pablo Serrano-Lorenzo, et al.Medicina Clinica|August 18, 2024
Adult Pompe disease: Analysis of 13 patientsPaloma Martín-Jiménez, Laura Bermejo-Guerrero, Ana Hernandez-Voth, et al.Journal of Critical Care Medicine (Universitatea De Medicina Si Farmacie Din Targu-Mures)|December 22, 2021
Plasmapheresis in the Treatment of Refractory Myoclonic Status. A Case ReportJudit Gutierrez-Gutierrez, Reyes Muñoz-Calahorro, Laura Bermejo-Guerrero, et al.Neurology|April 19, 2020
Miller Fisher syndrome and polyneuritis cranialis in COVID-19Consuelo Gutiérrez-Ortiz, Antonio Méndez-Guerrero, Sara Rodrigo-Rey, et al.Journal of Alzheimer'S Disease : JAD|October 24, 2019
Low Amyloid-PET Uptake in Iowa-Type Cerebral Amyloid Angiopathy with Cerebral Venous ThrombosisLaura Bermejo-Guerrero, Daniel Sánchez-Tejerina, Mario Sánchez-Tornero, et al.Journal of Neurology|May 6, 2020
Persistent asymptomatic or mild symptomatic hyperCKemia due to mutations in ANO5: the mildest end of the anoctaminopathies spectrumLuísa Panadés-de Oliveira, Laura Bermejo-Guerrero, Carlos Pablo de Fuenmayor-Fernández de la Hoz, et al.Journal of Clinical Medicine|May 13, 2023
Delayed Diagnosis of Congenital Myasthenic Syndromes Erroneously Interpreted as Mitochondrial MyopathiesMariana I Muñoz-García, María Paz Guerrero-Molina, Carlos Pablo de Fuenmayor-Fernández de la Hoz, et al.Journal of Neurology|November 1, 2023
Distal hereditary motor neuronopathy as a new phenotype associated with variants in BAG3Carlos Pablo de Fuenmayor-Fernández de la Hoz, Vincenzo Lupo, Laura Bermejo-Guerrero, et al.Molecular Genetics and Metabolism|January 24, 2025
Comprehensive analysis of GDF15 as a biomarker in primary mitochondrial myopathiesPaloma Martín-Jimenez, Laura Bermejo-Guerrero, María Navarro-Riquelme, et al.Neuromuscular Disorders : NMD|November 28, 2023
Distal myopathy due to digenic inheritance of TIA1 and SQSTM1 variants in two unrelated Spanish patientsLaura Bermejo-Guerrero, Carlos Pablo de Fuenmayor Fernández-de la Hoz, Lidia González-Quereda, et al.Pageof 2