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Author/Creator Neuser, Sonja

1. Clinical, neuroimaging, and molecular spectrum of TECPR2‐associated hereditary sensory and autonomic neuropathy with intellectual disability. Issue 6 (11th May 2021)

Authors:
Neuser, Sonja; Brechmann, Barbara; Heimer, Gali; Brösse, Ines; Schubert, Susanna; O'Grady, Lauren; Zech, Michael; Srivastava, Siddharth; Sweetser, David A.; Dincer, Yasemin; Mall, Volker; Winkelmann, Juliane; Behrends, Christian; Darras, Basil T.; Graham, Robert J.; Jayakar, Parul; Byrne, Barry; ...
Journal:
Human mutation
Issue:
Volume 42:Issue 6(2021)
Page Start:
762
Record Type:
Journal Article
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2. High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegia. Issue 4 (25th September 2021)

Authors:
Ebrahimi-Fakhari, Darius; Alecu, Julian E; Brechmann, Barbara; Ziegler, Marvin; Eberhardt, Kathrin; Jumo, Hellen; D'Amore, Angelica; Habibzadeh, Parham; Faghihi, Mohammad Ali; De Bleecker, Jan L; Vuillaumier-Barrot, Sandrine; Auvin, Stéphane; Santorelli, Filippo M; Neuser, Sonja; Popp, Bernt; Yan...
Journal:
Brain communications
Issue:
Volume 3:Issue 4(2021)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Pharmacological inhibition of focal segmental glomerulosclerosis‐related, gain of function mutants of TRPC6 channels by semi‐synthetic derivatives of larixol. (15th October 2017)

Authors:
Urban, Nicole; Neuser, Sonja; Hentschel, Anika; Köhling, Sebastian; Rademann, Jörg; Schaefer, Michael
Journal:
British journal of pharmacology
Issue:
Volume 174:Number 22(2017)
Page Start:
4099
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗