Eugenio Mercuri

Professor of Pediatric Neurology

Università Cattolica del Sacro Cuore

Italy

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Professor Eugenio Mercuri is a distinguished faculty member in Pediatric Neurology at the Università Cattolica del Sacro Cuore Sede di Roma, Italy. His research primarily focuses on spinal muscular atrophy, including the genetic underpinnings and management strategies for affected individuals. He has contributed significantly to the field through his recent publications, addressing topics such as disease-modifying therapies, language abilities in children with spinal muscular atrophy, and the harmonization of clinical assessment tools for dystrophinopathies.

Articles (18)

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2025

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2020

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2020

Collaborators (9)

Antonio G. deBelvis

Università Cattolica del Sacro Cuore

ITALY

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Anna Kostera-Pruszczyk

Head of Department/Prof.

Medical University of Warsaw

POLAND

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francesco danilo tiziano

Associate professor

Università Cattolica del Sacro Cuore Facoltà di Medicina e Chirurgia

ITALY

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Giovanni Baranello

Prof.

University College London

UNITED KINGDOM

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Gabriele Siciliano

Full Professor

University of Pisa

ITALY

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Piero Valentini

Università Cattolica del Sacro Cuore

ITALY

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odile boespflug-tanguy

Professor

Université Paris Diderot

FRANCE

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Lorenzo Fontanelli

University of Pisa

ITALY

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Tina Duong

Stanford University

UNITED STATES

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Eugenio Mercuri

Research Interests

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Articles (18)

Single Nucleotide SMN1 Variants in a Cohort of Individuals With Spinal Muscular Atrophy

Expressive language and social communication abilities in children with spinal muscular atrophy type 1

Corticosteroid therapy in Duchenne muscular dystrophy: Management and new insights

Pregnancy in the Era of Disease‐Modifying Therapies for Spinal Muscular Atrophy: Considerations From a Case Report

Italian survey on evolving SMA care with disease-modifying therapies: a consensus workshop on nutrition, swallowing, respiratory and rehabilitation care

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

JEWELFISH: 24-month results from an open-label study in non-treatment-naïve patients with SMA receiving treatment with risdiplam

Bulbar function in spinal muscular atrophy (SMA): State of art and new challenges. 21st July 2023, Rome, Italy

Towards harmonization of clinical tools for assessing Brain Involvement in Dystrophinopathies (BIND); report of four expert workshops: Newcastle, Leiden, Rome, Paris

Risdiplam in types 2 and 3 spinal muscular atrophy: A randomised, placebo‐controlled, dose‐finding trial followed by 24 months of treatment

New therapies for spinal muscular atrophy: where we stand and what is next

Scientific rationale for a higher dose of nusinersen

Contactless: a new personalised telehealth model in chronic pediatric diseases and disability during the COVID-19 era

Reply to: The need for evidence‐based treatment decisions in spinal muscular atrophy type 0

Spinal muscular atrophy: from rags to riches

Risdiplam treatment has not led to retinal toxicity in patients with spinal muscular atrophy

Nusinersen in type 0 spinal muscular atrophy: should we treat?

Patient and parent oriented tools to assess health-related quality of life, activity of daily living and caregiver burden in SMA. Rome, 13 July 2019

Collaborators (9)

Antonio G. deBelvis

Anna Kostera-Pruszczyk

francesco danilo tiziano

Giovanni Baranello

Gabriele Siciliano

Piero Valentini

odile boespflug-tanguy

Lorenzo Fontanelli

Tina Duong

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