1. A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease. Issue 7 (22nd February 2021) Authors: Liu, Hui; Koros, Christos; Strohäker, Timo; Schulte, Claudia; Bozi, Maria; Varvaresos, Stefanos; Ibáñez de Opakua, Alain; Simitsi, Athina Maria; Bougea, Anastasia; Voumvourakis, Konstantinos; Maniati, Matina; Papageorgiou, Sokratis G.; Hauser, Ann‐Kathrin; Becker, Stefan; Zweckstetter, Markus; St... Journal: Movement disorders Issue: Volume 36:Issue 7(2021) Page Start: 1624 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cognitive impairment in Glucocerebrosidase (GBA)‐associated PD: Not primarily associated with cerebrospinal fluid Abeta and Tau profiles. Issue 12 (2nd November 2017) Authors: Lerche, Stefanie; Schulte, Claudia; Srulijes, Karin; Pilotto, Andrea; Rattay, Tim W.; Hauser, Ann‐Kathrin; Stransky, Elke; Deuschle, Christian; Csoti, Ilona; Lachmann, Ingolf; Zetterberg, Henrik; Liepelt‐Scarfone, Inga; Gasser, Thomas; Maetzler, Walter; Berg, Daniela; Brockmann, Kathrin Journal: Movement disorders Issue: Volume 32:Issue 12(2017) Page Start: 1780 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. CSF Protein Level of Neurotransmitter Secretion, Synaptic Plasticity, and Autophagy in PD and DLB. Issue 11 (28th June 2021) Authors: Lerche, Stefanie; Sjödin, Simon; Brinkmalm, Ann; Blennow, Kaj; Wurster, Isabel; Roeben, Benjamin; Zimmermann, Milan; Hauser, Ann‐Kathrin; Liepelt‐Scarfone, Inga; Waniek, Katharina; Lachmann, Ingolf; Gasser, Thomas; Zetterberg, Henrik; Brockmann, Kathrin Journal: Movement disorders Issue: Volume 36:Issue 11(2021) Page Start: 2595 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Dementia with lewy bodies: GBA1 mutations are associated with cerebrospinal fluid alpha‐synuclein profile. Issue 7 (12th June 2019) Authors: Lerche, Stefanie; Machetanz, Gerrit; Wurster, Isabel; Roeben, Benjamin; Zimmermann, Milan; Pilotto, Andrea; Preische, Oliver; Stransky, Elke; Deuschle, Christian; Hauser, Ann‐Kathrin; Schulte, Claudia; Lachmann, Ingolf; Waniek, Katharina; Gasser, Thomas; Berg, Daniela; Maetzler, Walter; Brockmann... Journal: Movement disorders Issue: Volume 34:Issue 7(2019) Page Start: 1069 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. GBA‐associated Parkinson's disease: Reduced survival and more rapid progression in a prospective longitudinal study. Issue 3 (1st December 2014) Authors: Brockmann, Kathrin; Srulijes, Karin; Pflederer, Sylvia; Hauser, Ann‐Kathrin; Schulte, Claudia; Maetzler, Walter; Gasser, Thomas; Berg, Daniela Journal: Movement disorders Issue: Volume 30:Issue 3(2015) Page Start: 407 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. HPCA confirmed as a genetic cause of DYT2‐like dystonia phenotype. Issue 8 (25th August 2018) Authors: Atasu, Burcu; Hanagasi, Hasmet; Bilgic, Basar; Pak, Meltem; Erginel‐Unaltuna, Nihan; Hauser, Ann‐Kathrin; Guven, Gamze; Simón‐Sánchez, Javier; Heutink, Peter; Gasser, Thomas; Lohmann, Ebba Journal: Movement disorders Issue: Volume 33:Issue 8(2018) Page Start: 1354 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Mutations in CIZ1 are not a major cause for dystonia in Germany. Issue 5 (17th March 2015) Authors: Dufke, Claudia; Hauser, Ann‐Kathrin; Sturm, Marc; Fluhr, Susanne; Wächter, Tobias; Leube, Barbara; Auburger, Georg; Ott, Thomas; Bauer, Peter; Gasser, Thomas; Grundmann, Kathrin Journal: Movement disorders Issue: Volume 30:Issue 5(2015) Page Start: 740 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Parkinson's Disease: Glucocerebrosidase 1 Mutation Severity Is Associated with CSF Alpha‐Synuclein Profiles. Issue 3 (30th October 2019) Authors: Lerche, Stefanie; Wurster, Isabel; Roeben, Benjamin; Zimmermann, Milan; Riebenbauer, Benjamin; Deuschle, Christian; Hauser, Ann‐Kathrin; Schulte, Claudia; Berg, Daniela; Maetzler, Walter; Waniek, Katharina; Lachmann, Ingolf; Liepelt‐Scarfone, Inga; Gasser, Thomas; Brockmann, Kathrin Journal: Movement disorders Issue: Volume 35:Issue 3(2020) Page Start: 495 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Polygenic load: Earlier disease onset but similar longitudinal progression in Parkinson's disease. Issue 8 (22nd August 2018) Authors: Lerche, Stefanie; Liepelt‐Scarfone, Inga; Wurster, Isabel; Schulte, Claudia; Schäffer, Eva; Röben, Benjamin; Machetanz, Gerrit; Zimmermann, Milan; Akbas, Selda; Hauser, Ann‐Kathrin; Gasser, Thomas; Maetzler, Walter; Berg, Daniela; Brockmann, Kathrin Journal: Movement disorders Issue: Volume 33:Issue 8(2018) Page Start: 1349 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. SNCA: Major genetic modifier of age at onset of Parkinson's disease. Issue 9 (14th May 2013) Authors: Brockmann, Kathrin; Schulte, Claudia; Hauser, Ann‐Kathrin; Lichtner, Peter; Huber, Heiko; Maetzler, Walter; Berg, Daniela; Gasser, Thomas Journal: Movement disorders Issue: Volume 28:Issue 9(2013) Page Start: 1217 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗