1. Alpha synuclein and crystallin expression in human lens in Parkinson's disease. Issue 4 (16th February 2016) Authors: Klettner, Alexa; Richert, Elisabeth; Kuhlenbäumer, Gregor; Nölle, Bernhard; Bhatia, Kailash P.; Deuschl, Günter; Roider, Johann; Schneider, Susanne A. Journal: Movement disorders Issue: Volume 31:Issue 4(2016) Page Start: 600 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Atypical pantothenate kinase-associated neurodegeneration with variable phenotypes in an Egyptian family. Issue 7 (July 2021) Authors: Shalash, Ali S.; Rösler, Thomas W.; Abdelrahman, Ibrahim Y.; Abulmakarem, Hatem S.; Müller, Stefanie H.; Hopfner, Franziska; Kuhlenbäumer, Gregor; Höglinger, Günter U.; Salama, Mohamed Journal: Heliyon Issue: Volume 7:Issue 7(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Author response: Use of β2-adrenoreceptor agonist and antagonist drugs and risk of Parkinson disease. (19th May 2020) Authors: Pottegård, Anton; Hopfner, Franziska; Wod, Mette; Höglinger, Günter U.; Blaabjerg, Morten; Rösler, Thomas W.; Kuhlenbäumer, Gregor; Christensen, Kaare; Deuschl, Günther Journal: Neurology Issue: Volume 94:Number 20(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autosomal dominant burning feet syndrome. Issue 1 (1st July 1999) Authors: Stögbauer, Florian; Young, Peter; Kuhlenbäumer, Gregor; Kiefer, Reinhard; Timmerman, Vincent; Ringelstein, E Bernd; Wang, Jian-Feng; Schröder, J Michael; Van Broeckhoven, Christine; Weis, Joachim Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 67:Issue 1(1999) Page Start: 78 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Broad Phenotypic Heterogeneity due to a Novel SCN1A Mutation in a Family With Genetic Epilepsy With Febrile Seizures Plus. (February 2014) Authors: Goldberg-Stern, Hadassa; Aharoni, Sharon; Afawi, Zaid; Bennett, Odeya; Appenzeller, Silke; Pendziwiat, Manuela; Kuhlenbäumer, Gregor; Basel-Vanagaite, Lina; Shuper, Avinoam; Korczyn, Amos D.; Helbig, Ingo Journal: Journal of child neurology Issue: Volume 29:Number 2(2014:Feb.) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. C.207C>G mutation in sepiapterin reductase causes autosomal dominant dopa-responsive dystonia. (December 2017) Authors: Shalash, Ali S.; Rösler, Thomas W.; Müller, Stefanie H.; Salama, Mohamed; Deuschl, Günther; Müller, Ulrich; Opladen, Thomas; Petersen, Britt-Sabina; Franke, Andre; Hopfner, Franziska; Kuhlenbäumer, Gregor; Höglinger, Günter U. Journal: Neurology Issue: Volume 3:Number 6(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Common Variants Near ZIC1 and ZIC4 in Autopsy‐Confirmed Multiple System Atrophy. Issue 10 (23rd August 2022) Authors: Hopfner, Franziska; Tietz, Anja K.; Ruf, Viktoria C.; Ross, Owen A.; Koga, Shunsuke; Dickson, Dennis; Aguzzi, Adriano; Attems, Johannes; Beach, Thomas; Beller, Allison; Cheshire, William P.; van Deerlin, Vivianna; Desplats, Paula; Deuschl, Günther; Duyckaerts, Charles; Ellinghaus, David; Evsyukov... Journal: Movement disorders Issue: Volume 37:Issue 10(2022) Page Start: 2110 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Early-onset parkinsonism due to compound heterozygous POLG mutations. (August 2016) Authors: Rempe, Torge; Kuhlenbäumer, Gregor; Krüger, Stefanie; Biskup, Saskia; Matschke, Jakob; Hagel, Christian; Deuschl, Günther; van Eimeren, Thilo Journal: Parkinsonism & related disorders Issue: Volume 29(2016) Page Start: 135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Early‐ and late‐onset essential tremor patients represent clinically distinct subgroups. Issue 10 (6th October 2016) Authors: Hopfner, Franziska; Ahlf, Anjuli; Lorenz, Delia; Klebe, Stephan; Zeuner, Kirsten E.; Kuhlenbäumer, Gregor; Deuschl, Günther Journal: Movement disorders Issue: Volume 31:Issue 10(2016) Page Start: 1560 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting. (29th January 2019) Authors: Chauhan, Ganesh; Adams, Hieab H.H.; Satizabal, Claudia L.; Bis, Joshua C.; Teumer, Alexander; Sargurupremraj, Muralidharan; Hofer, Edith; Trompet, Stella; Hilal, Saima; Smith, Albert Vernon; Jian, Xueqiu; Malik, Rainer; Traylor, Matthew; Pulit, Sara L.; Amouyel, Philippe; Mazoyer, Bernard; Zhu, Y... Journal: Neurology Issue: Volume 92:Number 5(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗