Publications by authors named "K Vill"

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Treatment evolution in spinal muscular atrophy: insights from the SMArtCARE registry.
Cornelia Voigt-Müller, Michelle Pfaffenlehner, Günther Bernert, Hakan Cetin, Tim Hagenacker, Katharina Vill

Brain· December 2025

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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, Günther Bernert, Astrid Blaschek

J Neuromuscul Dis· November 2025

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Quality of Life of Children and Adolescents with Epilepsy Compared to Their Healthy Peers: A Cross-Sectional Study.
Robert Opitz, Miriam Gerstner, Lena Mühe, Malin Zaddach, Leonie Grosse, Katharina Vill

Neuropediatrics· September 2025

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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, Theresa Brunet, Hannah Klinkhammer, Katharina Vill

Nat Genet· July 2025

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Loss of DOT1L disrupts neuronal transcription and leads to a neurodevelopmental disorder.
Marissa J Maroni, Melissa Barton, Katherine Lynch, Ashish R Deshwar, Philip D Campbell, Katharina Vill

Brain· June 2025

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