Francesco Catapano

UCL Queen Square Institute Of Neurology, Queen Square
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 19 publications

Muscle transcriptome profiling reveals novel molecular pathways and biomarkers in laminin-α2 deficient patients.

Muscle transcriptome profiling reveals novel molecular pathways and biomarkers in laminin-α2 deficient patients.

Journal: Acta neuropathologica communications

Published: September 26, 2025

A comprehensive spatiotemporal map of dystrophin isoform expression in the developing and adult human brain.

A comprehensive spatiotemporal map of dystrophin isoform expression in the developing and adult human brain.

Journal: Acta neuropathologica communications

Published: December 27, 2024

Recurrent de novo SPTLC2 variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis.

Recurrent de novo SPTLC2 variant causes childhood-onset amyotrophic lateral sclerosis (ALS) by excess sphingolipid synthesis.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: July 07, 2023

T Cell Responses to Dystrophin in a Natural History Study of Duchenne Muscular Dystrophy.

T Cell Responses to Dystrophin in a Natural History Study of Duchenne Muscular Dystrophy.

Journal: Human gene therapy

Published: December 01, 2022

Microvasculopathy in spinal muscular atrophy is driven by a reversible autonomous endothelial cell defect.

Microvasculopathy in spinal muscular atrophy is driven by a reversible autonomous endothelial cell defect.

Journal: The Journal of clinical investigation

Published: July 26, 2021

The administration of antisense oligonucleotide golodirsen reduces pathological regeneration in patients with Duchenne muscular dystrophy.

The administration of antisense oligonucleotide golodirsen reduces pathological regeneration in patients with Duchenne muscular dystrophy.

Journal: Acta neuropathologica communications

Published: December 11, 2020

The altered expression of neurofilament in mouse models and patients with spinal muscular atrophy.

The altered expression of neurofilament in mouse models and patients with spinal muscular atrophy.

Journal: Annals of clinical and translational neurology

Published: December 03, 2020

Novel free-circulating and extracellular vesicle-derived miRNAs dysregulated in Duchenne muscular dystrophy.

Novel free-circulating and extracellular vesicle-derived miRNAs dysregulated in Duchenne muscular dystrophy.

Journal: Epigenomics

Published: November 20, 2020

Novel Applications of Mesenchymal Stem Cell-derived Exosomes for Myocardial Infarction Therapeutics.

Novel Applications of Mesenchymal Stem Cell-derived Exosomes for Myocardial Infarction Therapeutics.

Journal: Biomolecules

Published: April 01, 2020

Bioinspired artificial exosomes based on lipid nanoparticles carrying let-7b-5p promote angiogenesis in vitro and in vivo.

Bioinspired artificial exosomes based on lipid nanoparticles carrying let-7b-5p promote angiogenesis in vitro and in vivo.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: March 12, 2020

A high-throughput digital script for multiplexed immunofluorescent analysis and quantification of sarcolemmal and sarcomeric proteins in muscular dystrophies.

A high-throughput digital script for multiplexed immunofluorescent analysis and quantification of sarcolemmal and sarcomeric proteins in muscular dystrophies.

Journal: Acta neuropathologica communications

Published: January 31, 2020

Exosomes Could Offer New Options to Combat the Long-Term Complications Inflicted by Gestational Diabetes Mellitus.

Exosomes Could Offer New Options to Combat the Long-Term Complications Inflicted by Gestational Diabetes Mellitus.

Journal: Cells

Published: January 04, 2020

Showing 1-12 of 19

Last Updated: 09/26/2026