Claudia Weiß
6PUBLICATIONS
59CO-AUTHORS
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Publications (6)
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|Apr 11, 2026
Risdiplam Add-On Therapy Following Onasemnogene Abeparvovec in Children With Spinal Muscular Atrophy and 2 SMN2 Copies: A Multi-Center Case Series.Corinna Stoltenburg, Klaus Goldhahn, Arpad von Moers
|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
|Jun 24, 2025
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.Axel Schmidt, Magdalena Danyel, Kathrin Grundmann
|May 12, 2025
3D Electron Microscopic Visualization of Nemaline Rods in a Case of Congenital Myopathy.Carsten Dittmayer, Hans H Goebel, Claudia Weiß
|Jul 22, 2024
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings.Axel Schmidt, Magdalena Danyel, Kathrin Grundmann
|May 16, 2024
A Mild But Typical Presentation of Bethlem Myopathy With a Novel In-Frame Deletion in COL6A1: Almost Overlooked.Nina-Maria Wilpert, Markus Schuelke, Birgit Lala
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Frequent Collaborators
4 joint publications
Markus Schülke
2 joint publications
Axel Schmidt
2 joint publications
Theresa Brunet
2 joint publications
Hannah Klinkhammer
2 joint publications
Tzung-Chien Hsieh
2 joint publications
Hartmut Engels
2 joint publications
Alexej Knaus
2 joint publications
Shahida Moosa
2 joint publications
Jean Tori Pantel
2 joint publications
Julia Neugebauer
