Laura Guerrero-Bermejo

Madrid, MD, Spain

Last Updated: 09/26/2026

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Found 23 publications

Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study.

Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study.

Journal: Neurology

Published: January 15, 2026

Multidimensional assessment of diaphragmatic dysfunction in late-onset Pompe disease: a prospective cohort study.

Multidimensional assessment of diaphragmatic dysfunction in late-onset Pompe disease: a prospective cohort study.

Journal: Orphanet journal of rare diseases

Published: January 12, 2026

Clinical Heterogeneity and Candidate Biomarkers in POLG-Related Mitochondrial Disease.

Clinical Heterogeneity and Candidate Biomarkers in POLG-Related Mitochondrial Disease.

Journal: Neurology. Genetics

Published: July 11, 2025

Exploring Outcome Measures for Mitochondrial Myopathies; Insights From a Longitudinal Study on TK2 Deficiency.

Exploring Outcome Measures for Mitochondrial Myopathies; Insights From a Longitudinal Study on TK2 Deficiency.

Journal: Journal of inherited metabolic disease

Published: June 11, 2025

Myo-Guide: A Machine Learning-Based Web Application for Neuromuscular Disease Diagnosis With MRI.

Myo-Guide: A Machine Learning-Based Web Application for Neuromuscular Disease Diagnosis With MRI.

Journal: Journal of cachexia, sarcopenia and muscle

Published: September 18, 2024

Comprehensive analysis of GDF15 as a biomarker in primary mitochondrial myopathies.

Comprehensive analysis of GDF15 as a biomarker in primary mitochondrial myopathies.

Journal: Molecular genetics and metabolism

Published: August 23, 2024

Adult Pompe disease: Analysis of 13 patients

Adult Pompe disease: Analysis of 13 patients

Journal: Medicina clinica

Published: March 25, 2024

Expanding the Clinical Spectrum of DRP2-Associated Charcot-Marie-Tooth Disease.

Expanding the Clinical Spectrum of DRP2-Associated Charcot-Marie-Tooth Disease.

Journal: Neurology

Published: March 21, 2024

Remarkable clinical improvement with oral nucleoside treatment in a patient with adult-onset TK2 deficiency: A case report.

Remarkable clinical improvement with oral nucleoside treatment in a patient with adult-onset TK2 deficiency: A case report.

Journal: Mitochondrion

Published: January 10, 2024

Clinical and Genetic Analysis of Patients With TK2 Deficiency.

Clinical and Genetic Analysis of Patients With TK2 Deficiency.

Journal: Neurology. Genetics

Published: December 04, 2023

Distal hereditary motor neuronopathy as a new phenotype associated with variants in BAG3.

Distal hereditary motor neuronopathy as a new phenotype associated with variants in BAG3.

Journal: Journal of neurology

Published: September 12, 2023

Distal myopathy due to digenic inheritance of TIA1 and SQSTM1 variants in two unrelated Spanish patients.

Distal myopathy due to digenic inheritance of TIA1 and SQSTM1 variants in two unrelated Spanish patients.

Journal: Neuromuscular disorders : NMD

Published: May 25, 2023

Showing 1-12 of 23

Last Updated: 09/26/2026