Ramon Marti

Barcelona, CT, Spain

Last Updated: 09/26/2026

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Found 67 publications

Systemic Mitochondrial DNA Kinetics After cDCD Lung Transplantation Do Not Reflect Donor Warm Ischemic Injury: DACMEDAMPs, a Prospective multicenter translational study.

Systemic Mitochondrial DNA Kinetics After cDCD Lung Transplantation Do Not Reflect Donor Warm Ischemic Injury: DACMEDAMPs, a Prospective multicenter translational study.

Journal: American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
Published: February 12, 2026

Equilibrative nucleoside transporter 1 deficiency protects against diet-induced MASLD and is stage-associated in human liver disease.

Equilibrative nucleoside transporter 1 deficiency protects against diet-induced MASLD and is stage-associated in human liver disease.

Journal: Metabolism: clinical and experimental
Published: January 21, 2026

Systemic delivery of AAV-GFM1 corrects COXPD1 molecular alterations in Gfm1R671C/- mice.

Systemic delivery of AAV-GFM1 corrects COXPD1 molecular alterations in Gfm1R671C/- mice.

Journal: EMBO molecular medicine
Published: October 03, 2025

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

NK-A 17E-233I: a novel competitive inhibitor of human dihydroorotate dehydrogenase (DHODH) for cancer therapy.

NK-A 17E-233I: a novel competitive inhibitor of human dihydroorotate dehydrogenase (DHODH) for cancer therapy.

Journal: Journal of experimental & clinical cancer research : CR
Published: April 01, 2025

Successful AAV8 gene therapy on hepatic ex situ machine perfusion for mitochondrial neurogastrointestinal encephalomyopathy.

Successful AAV8 gene therapy on hepatic ex situ machine perfusion for mitochondrial neurogastrointestinal encephalomyopathy.

Journal: Journal of hepatology
Published: February 23, 2025

Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease.

Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease.

Journal: Annals of neurology
Published: June 03, 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

Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation.

Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation.

Journal: Orphanet journal of rare diseases
Published: March 22, 2023

Distinctive gastrointestinal motor dysfunction in patients with MNGIE.

Distinctive gastrointestinal motor dysfunction in patients with MNGIE.

Journal: Neurogastroenterology and motility
Published: February 16, 2023

Identification of two novel RRM2B variants associated with autosomal recessive progressive external ophthalmoplegia in a family with pseudodominant inheritance pattern.

Identification of two novel RRM2B variants associated with autosomal recessive progressive external ophthalmoplegia in a family with pseudodominant inheritance pattern.

Journal: Journal of human genetics
Published: September 26, 2022

Pathological Features in Paediatric Patients with TK2 Deficiency.

Pathological Features in Paediatric Patients with TK2 Deficiency.

Journal: International journal of molecular sciences
Published: August 12, 2022
Showing 1-12 of 67

Last Updated: 09/26/2026