Claudia Castiglioni

13PUBLICATIONS
112CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Liquid biopsiesMedical molecular engineering of nucleic acids and proteinsCardiology (incl. cardiovascular diseases)
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Publications (13)

|Jan 19, 2026
International Registry of NKX2-1-Related Disorders: Clinical, Genetic, and Imaging Perspectives.

Laia Nou-Fontanet, Claudia Ravelli, Lydie Burglen

|May 21, 2025
Patient and caregiver spinal muscular atrophy treatment attribute preferences in Latin America.

Victoria Saenz, Marijana Chlistalla, Nayara Carlos

|Mar 13, 2025
Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration.

Stefan Groeneweg, Ferdy S van Geest, Mariano Martín

|Jan 08, 2025
Imaging-Based Molecular Interaction Between Src and Lamin A/C Mechanosensitive Proteins in the Nucleus of Laminopathic Cells.

Stefania Petrini, Giulia Bagnato, Michela Piccione

|Dec 18, 2023
Life-Saving Treatments for Spinal Muscular Atrophy: Global Access and Availability.

Victor D Armengol, Basil T Darras, Ahmad A Abulaban

|Aug 12, 2022
Deep Molecular Characterization of Milder Spinal Muscular Atrophy Patients Carrying the c.859G>C Variant in SMN2

Laura Blasco-Pérez, Mar Costa-Roger, Jordi Leno-Colorado

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Frequent Collaborators

3 joint publications

Edmar Zanoteli

2 joint publications

Andres Lozano-Arango

2 joint publications

André M S Silva

2 joint publications

Eduardo F Tizzano