Giovanni Baranello

Prof.

University College London

United Kingdom

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Professor Giovanni Baranello is a faculty member at University College London in the United Kingdom. His research primarily focuses on muscular dystrophies and spinal muscular atrophy, with recent articles addressing topics such as dystrophin isoform deficiency, gene therapy applications, and the impact of treatments on motor function and ambulation. Professor Baranello's work contributes significantly to understanding and improving clinical outcomes in pediatric neuromuscular disorders.

Articles (19)

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2025

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2020

Collaborators (8)

Eugenio Mercuri

Professor of Pediatric Neurology

Università Cattolica del Sacro Cuore

ITALY

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Evelin Milev

University College London

UNITED KINGDOM

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Francesco Muntoni

University College London

UNITED KINGDOM

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MARIA FOSCAN

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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matilde leonardi

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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Kayoko Saito

Director & Professor

Tokyo Women's Medical University

JAPAN

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Robert Muni-Lofra

Newcastle University

UNITED KINGDOM

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nathalie goemans

associate professor- Emeritus

Katholieke Universiteit Leuven

BELGIUM

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Giovanni Baranello

Research Interests

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Articles (19)

Safety and Efficacy of IV Onasemnogene Abeparvovec for Pediatric Patients With Spinal Muscular Atrophy

Dystrophin isoform deficiency and upper‐limb and respiratory function in Duchenne muscular dystrophy

Bulbar function in children with spinal muscular atrophy type 1 treated with nusinersen

Construct Validity and Internal Consistency of the Italian Version of the PedsQL<sup>TM</sup> 4.0 Generic Core Scale and PedsQL<sup>TM</sup> 3.0 Cerebral Palsy Module

Fully personalized modelling of Duchenne Muscular Dystrophy ambulation

Relationship between growth and ambulation loss in Duchenne muscular dystrophy boys on steroids

AAV gene therapy for Duchenne Muscular Dystrophy: lessons learned from a phase 3 trial

Interpreting motor function outcomes in young males with Duchenne muscular dystrophy

Efficacy and safety of onasemnogene abeparvovec in children with spinal muscular atrophy type 1: real-world evidence from 6 infusion centres in the United Kingdom

The emerging spectrum of neurodevelopmental comorbidities in early-onset Spinal Muscular Atrophy

Correction to: Two‑year efficacy and safety of risdiplam in patients with type 2 or non‑ambulant type 3 spinal muscular atrophy (SMA)

Two-year efficacy and safety of risdiplam in patients with type 2 or non-ambulant type 3 spinal muscular atrophy (SMA)

2-Year Change in Revised Hammersmith Scale Scores in a Large Cohort of Untreated Paediatric Type 2 and 3 SMA Participants

Can Breathing Pattern Assessment Predict the Need of Ventilatory Support in Treated Infants with Spinal Muscular Atrophy Type 1?

Risdiplam-Treated Infants with Type 1 Spinal Muscular Atrophy versus Historical Controls

Brain, cognition, and language development in spinal muscular atrophy type 1: a scoping review

Risdiplam in Type 1 Spinal Muscular Atrophy

Reply to Chacko et al.: Limited Assessment of Respiratory Muscle Response to Nusinersen Treatment in Infants with Spinal Muscular Atrophy

Visual Function Classification System for children with cerebral palsy: development and validation

Collaborators (8)

Eugenio Mercuri

Evelin Milev

Francesco Muntoni

MARIA FOSCAN

matilde leonardi

Kayoko Saito

Robert Muni-Lofra

nathalie goemans

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