Federica Montanaro
UCL Great Ormond Street Institute Of Child Health
London, ENG WC1N1EH, United Kingdom
London, ENG WC1N1EH, United Kingdom
Last Updated: 09/26/2026
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Found 22 publications
Regional Expression of Dystrophin Gene Transcripts and Proteins in the Mouse Brain.
Journal: Cells
Published: August 06, 2025
Behavioral improvement in dystrophic mdx23 mouse following repeated antisense oligonucleotides injections.
Journal: Molecular therapy. Nucleic acids
Published: April 23, 2025
Impact of fever on the outcome non-anoxic acute brain injury patients: a systematic review and meta-analysis.
Journal: Critical care (London, England)
Published: September 06, 2024
Impact of distinct dystrophin gene mutations on behavioral phenotypes of Duchenne muscular dystrophy.
Journal: Disease models & mechanisms
Published: January 23, 2024
Networking to Optimize Dmd exon 53 Skipping in the Brain of mdx52 Mouse Model.
Journal: Biomedicines
Published: September 19, 2023
Aberrations in Energetic Metabolism and Stress-Related Pathways Contribute to Pathophysiology in the Neb Conditional Knockout Mouse Model of Nemaline Myopathy.
Journal: The American journal of pathology
Published: December 01, 2022
Different Mouse Models of Nemaline Myopathy Harboring Acta1 Mutations Display Differing Abnormalities Related to Mitochondrial Biology.
Journal: The American journal of pathology
Published: December 01, 2022
Cerebro-spinal fluid glucose and lactate concentrations changes in response to therapies in patIents with primary brain injury: the START-TRIP study.
Journal: Critical care (London, England)
Published: November 17, 2022
Evaluation of the dystrophin carboxy-terminal domain for micro-dystrophin gene therapy in cardiac and skeletal muscles in the DMDmdx rat model.
Journal: Gene therapy
Published: April 12, 2021
Proteomic analysis identifies key differences in the cardiac interactomes of dystrophin and micro-dystrophin.
Journal: Human molecular genetics
Published: March 24, 2021
Cardiac-Specific Expression of ΔH2-R15 Mini-Dystrophin Normalized All Electrocardiogram Abnormalities and the End-Diastolic Volume in a 23-Month-Old Mouse Model of Duchenne Dilated Cardiomyopathy.
Journal: Human gene therapy
Published: February 13, 2018
Last Updated: 09/26/2026