1. A look inside the nerve – Morphology of nerve fascicles in healthy controls and patients with polyneuropathy. Issue 12 (December 2017) Authors: Grimm, Alexander; Winter, Natalie; Rattay, Tim W.; Härtig, Florian; Dammeier, Nele M.; Auffenberg, Eva; Koch, Marilin; Axer, Hubertus Journal: Clinical neurophysiology Issue: Volume 128:Issue 12(2017:Dec.) Page Start: 2521 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Characteristics of serum neurofilament light chain as a biomarker in hereditary spastic paraplegia type 4. Issue 3 (16th February 2022) Authors: Kessler, Christoph; Serna‐Higuita, Lina Maria; Wilke, Carlo; Rattay, Tim W.; Hengel, Holger; Reichbauer, Jennifer; Stransky, Elke; Leyva‐Gutiérrez, Alejandra; Mengel, David; Synofzik, Matthis; Schöls, Ludger; Martus, Peter; Schüle, Rebecca Journal: Annals of clinical and translational neurology Issue: Volume 9:Issue 3(2022) Page Start: 326 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 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) ↗
4. De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia. Issue 6 (12th February 2022) Authors: Van de Vondel, Liedewei; De Winter, Jonathan; Beijer, Danique; Coarelli, Giulia; Wayand, Melanie; Palvadeau, Robin; Pauly, Martje G.; Klein, Katrin; Rautenberg, Maren; Guillot‐Noël, Léna; Deconinck, Tine; Vural, Atay; Ertan, Sibel; Dogu, Okan; Uysal, Hilmi; Brankovic, Vesna; Herzog, Rebecca; Bric... Journal: Movement disorders Issue: Volume 37:Issue 6(2022) Page Start: 1175 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Freezing of Swallowing. Issue 5 (18th January 2016) Authors: Maetzler, Walter; Rattay, Tim W.; Hobert, Markus A.; Synofzik, Matthis; Bader, Angela; Berg, Daniela; Schaeffer, Eva; Rommel, Natalie; Devos, David; Bloem, Bastiaan R.; Bender, Benjamin Journal: Movement disorders clinical practice Issue: Volume 3:Issue 5(2016) Page Start: 490 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Late adult-onset pure spinal muscular atrophy due to a compound HEXB macro-deletion. Issue 7 (December 2013) Authors: Rattay, Tim W.; Schöls, Ludger; Wilhelm, Christian; Synofzik, Matthis Journal: Amyotrophic lateral sclerosis and frontotemporal degeneration Issue: Volume 14:Issue 7/8(2013) Page Start: 628 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia. Issue 5 (5th April 2021) Authors: Kessler, Christoph; Serna‐Higuita, Lina M.; Rattay, Tim W.; Maetzler, Walter; Wurster, Isabel; Hayer, Stefanie; Wilke, Carlo; Hengel, Holger; Reichbauer, Jennifer; Armbruster, Marcel; Schöls, Ludger; Martus, Peter; Schüle, Rebecca Journal: Annals of clinical and translational neurology Issue: Volume 8:Issue 5(2021) Page Start: 1122 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Serum neurofilament light chain is increased in hereditary spastic paraplegias. Issue 7 (21st May 2018) Authors: Wilke, Carlo; Rattay, Tim W.; Hengel, Holger; Zimmermann, Milan; Brockmann, Kathrin; Schöls, Ludger; Kuhle, Jens; Schüle, Rebecca; Synofzik, Matthis Journal: Annals of clinical and translational neurology Issue: Volume 5:Issue 7(2018) Page Start: 876 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Specific Gait Changes in Prodromal Hereditary Spastic Paraplegia Type 4: preSPG4 Study. Issue 12 (29th August 2022) Authors: Laßmann, Christian; Ilg, Winfried; Schneider, Marc; Völker, Maximilian; Haeufle, Daniel F.B.; Schüle, Rebecca; Giese, Martin; Synofzik, Matthis; Schöls, Ludger; Rattay, Tim W. Journal: Movement disorders Issue: Volume 37:Issue 12(2022) Page Start: 2417 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Ultrasound assessment of peripheral nerve pathology in neurofibromatosis type 1 and 2. Issue 5 (May 2017) Authors: Winter, Natalie; Rattay, Tim W.; Axer, Hubertus; Schäffer, Eva; Décard, Bernhard F.; Gugel, Isabel; Schuhmann, Martin; Grimm, Alexander Journal: Clinical neurophysiology Issue: Volume 128:Issue 5(2017:May) Page Start: 702 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗