Georg Martin Stettner

7PUBLICATIONS
53CO-AUTHORS
Molecular targetsNeurology and neuromuscular diseasesGene and molecular therapyPeripheral nervous systemNeonatology
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Publications (7)

|Aug 27, 2026
Delphi consensus on gene therapy of spinal muscular atrophy with onasemnogene abeparvovec in Germany, Austria and Switzerland - part II - expert based recommendations for surveillance and management of side-effects.

|Feb 24, 2026
Developing, Implementing, and Evaluating a Care Management Model for Patients With Neuromuscular Diseases: Protocol for a Participatory Mixed Methods Study.

Veronika Waldboth, Christina Schuler, Raffaella Willmann

|Nov 24, 2025
Delphi consensus on gene therapy of spinal muscular atrophy with onasemnogene abeparvovec in Germany, Austria and Switzerland-part I-systematic literature review and existing evidence.

Claudia Weiß, Katharina Vill, Matthias Baumann

|May 25, 2024
Chronic Pain in Patients with Spinal Muscular Atrophy in Switzerland: A Query to the Spinal Muscular Atrophy Registry.

Leonie Steiner, Anne Tscherter, Bettina Henzi

|Feb 27, 2024
SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation.

Marwan Nashabat, Nasrinsadat Nabavizadeh, Hilal Pırıl Saraçoğlu

|Aug 27, 2021
Differential Diagnosis of Acquired and Hereditary Neuropathies in Children and Adolescents-Consensus-Based Practice Guidelines.

Rudolf Korinthenberg, Regina Trollmann, Barbara Plecko

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Frequent Collaborators

2 joint publications

Andreas Ziegler

2 joint publications

Katharina Vill

2 joint publications

Claudia Weiß

1 joint publications

Martin Knoblauch