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Author/Creator Weng, Rosa

1. Clinico‐genetic spectrum of limb‐girdle muscular weakness in Austria: A multicentre cohort study. (10th March 2022)

Authors:
Krenn, Martin; Tomschik, Matthias; Wagner, Matias; Zulehner, Gudrun; Weng, Rosa; Rath, Jakob; Klotz, Sigrid; Gelpi, Ellen; Bsteh, Gabriel; Keritam, Omar; Colonna, Isabella; Paternostro, Chiara; Jäger, Fiona; Lindeck‐Pozza, Elisabeth; Iglseder, Stephan; Grinzinger, Susanne; Schönfelder, Martina; H...
Journal:
European journal of neurology
Issue:
Volume 29:Number 6(2022)
Page Start:
1815
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Connectome Analysis in an Individual with SETD1B-Related Neurodevelopmental Disorder and Epilepsy. Issue 6 (6th August 2022)

Authors:
Weng, Rosa; Nenning, Karl-Heinz; Schwarz, Michelle; Riedhammer, Korbinian M.; Brunet, Theresa; Wagner, Matias; Kasprian, Gregor; Lehrner, Johann; Zimprich, Fritz; Bonelli, Silvia B.; Krenn, Martin
Journal:
Journal of developmental and behavioral pediatrics
Issue:
Volume 43:Issue 6(2022)
Page Start:
e419
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Short‐term and sustained clinical response following thymectomy in patients with myasthenia gravis. (30th April 2022)

Authors:
Rath, Jakob; Taborsky, Manuela; Moser, Bernhard; Zulehner, Gudrun; Weng, Rosa; Krenn, Martin; Cetin, Hakan; Matilla, José Ramon; Müllauer, Leonhard; Zimprich, Fritz
Journal:
European journal of neurology
Issue:
Volume 29:Number 8(2022)
Page Start:
2453
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗