21. Capturing schizophrenia-like prodromal symptoms in a spinocerebellar ataxia-17 transgenic rat. (April 2017) Authors: Amato, Davide; Canneva, Fabio; Nguyen, Huu Phuc; Bauer, Peter; Riess, Olaf; von Hörsten, Stephan; Müller, Christian P Journal: Journal of psychopharmacology Issue: Volume 31:Number 4(2017) Page Start: 461 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
22. Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia. (5th September 2017) Authors: Giordano, Ilaria; Harmuth, Florian; Jacobi, Heike; Paap, Brigitte; Vielhaber, Stefan; Machts, Judith; Schöls, Ludger; Synofzik, Matthis; Sturm, Marc; Tallaksen, Chantal; Wedding, Iselin M.; Boesch, Sylvia; Eigentler, Andreas; van de Warrenburg, Bart; van Gaalen, Judith; Kamm, Christoph; Dudesek, ... Journal: Neurology Issue: Volume 89:Number 10(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
23. CNTNAP1 mutations cause CNS hypomyelination and neuropathy with or without arthrogryposis. (April 2017) Authors: Hengel, Holger; Magee, Alex; Mahanjah, Muhammad; Vallat, Jean-Michel; Ouvrier, Robert; Abu-Rashid, Mohammad; Mahamid, Jamal; Schüle, Rebecca; Schulze, Martin; Krägeloh-Mann, Ingeborg; Bauer, Peter; Züchner, Stephan; Sharkia, Rajech; Schöls, Ludger Journal: Neurology Issue: Volume 3:Number 2(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
24. Comment on 'A critical evaluation of the current "p‐value controversy" '. Issue 5 (21st April 2017) Authors: Bauer, Peter Journal: Biometrical journal Issue: Volume 59:Issue 5(2017:Sep.) Page Start: 873 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
25. Comments on 'Estimands in clinical trials – broadening the perspective'. (15th January 2017) Authors: Bauer, Peter Journal: Statistics in medicine Issue: Volume 36:Number 1(2017) Page Start: 22 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
26. De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function. (November 2018) Authors: Synofzik, Matthis; Helbig, Katherine; Harmuth, Florian; Deconinck, Tine; Tanpaiboon, Pranoot; Sun, Bo; Guo, Wenting; Wang, Ruiwu; Palmaer, Erika; Tang, Sha; Schaefer, G.; Gburek-Augustat, Janina; Züchner, Stephan; Krägeloh-Mann, Ingeborg; Baets, Jonathan; Jonghe, Peter; Bauer, Peter; Chen, S.; Sc... Journal: European journal of human genetics Issue: Volume 26:Number 11(2018) Page Start: 1623 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
27. Economic Analysis and Policy in Underdeveloped Countries. (2013) Authors: Bauer, Peter Record Type: Book Extent: 1 online resource (168 pages) View Content: Available online (eLD content is only available in our Reading Rooms) ↗
28. Editorial for the Quarterly Journal's special issue on Polar Prediction. (January 2016) Authors: Bauer, Peter; Jung, Thomas Journal: Quarterly journal of the Royal Meteorological Society Issue: Volume 142:Number 695(2016) Page Start: 537 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
29. EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia. Issue 3 (15th December 2020) Authors: Kuipers, Demy J. S.; Mandemakers, Wim; Lu, Chin‐Song; Olgiati, Simone; Breedveld, Guido J.; Fevga, Christina; Tadic, Vera; Carecchio, Miryam; Osterman, Bradley; Sagi‐Dain, Lena; Wu‐Chou, Yah‐Huei; Chen, Chiung C.; Chang, Hsiu‐Chen; Wu, Shey‐Lin; Yeh, Tu‐Hsueh; Weng, Yi‐Hsin; Elia, Antonio E.; Pan... Journal: Annals of neurology Issue: Volume 89:Issue 3(2021) Page Start: 485 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
30. EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts. Issue 1 (3rd November 2014) Authors: Huttenlocher, Johanna; Krüger, Rejko; Capetian, Philipp; Lohmann, Katja; Brockmann, Kathrin; Csoti, Ilona; Klein, Christine; Berg, Daniela; Gasser, Thomas; Bonin, Michael; Riess, Olaf; Bauer, Peter Journal: Journal of medical genetics Issue: Volume 52:Issue 1(2015) Page Start: 37 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗