Pablo Lorenzo-Serrano

Madrid, MD 28029, Spain

Last Updated: 09/26/2026

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Found 22 publications

Impact of compound heterozygous SDHA variants on mitochondrial function in pediatric with neurological disease.

Impact of compound heterozygous SDHA variants on mitochondrial function in pediatric with neurological disease.

Journal: Mitochondrion
Published: November 21, 2025

Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8.

Natural History of Patients With Mitochondrial ATPase Deficiency Due to Pathogenic Variants of MT-ATP6 and MT-ATP8.

Journal: Neurology
Published: March 20, 2025

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

Identification of a novel transcript of mouse Sdha.

Identification of a novel transcript of mouse Sdha.

Journal: BMC research notes
Published: July 16, 2024

Succinate Dehydrogenase and Human Disease: Novel Insights into a Well-Known Enzyme.

Succinate Dehydrogenase and Human Disease: Novel Insights into a Well-Known Enzyme.

Journal: Biomedicines
Published: July 09, 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

Development of a novel in vitro model to study the modulatory role of the respiratory complex I in macrophage effector functions.

Development of a novel in vitro model to study the modulatory role of the respiratory complex I in macrophage effector functions.

Journal: PloS one
Published: February 19, 2023

Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome.

Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome.

Journal: Journal of clinical medicine
Published: February 15, 2023

The mitochondrial succinate dehydrogenase complex controls the STAT3-IL-10 pathway in inflammatory macrophages.

The mitochondrial succinate dehydrogenase complex controls the STAT3-IL-10 pathway in inflammatory macrophages.

Journal: iScience
Published: December 15, 2022

A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene.

A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene.

Journal: International journal of molecular sciences
Published: November 09, 2022

Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the LDHA Gene (GSD XI).

Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the LDHA Gene (GSD XI).

Journal: Genes
Published: September 16, 2022
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Last Updated: 09/26/2026