1. Antibody response after COVID‐19 vaccination in intravenous immunoglobulin‐treated immune neuropathies. (8th August 2022) Authors: Svačina, Martin K. R.; Meißner, Anika; Schweitzer, Finja; Ladwig, Anne; Sprenger‐Svačina, Alina; Klein, Ines; Wüstenberg, Hauke; Kohle, Felix; Schneider, Christian; Grether, Nicolai B.; Wunderlich, Gilbert; Fink, Gereon R.; Klein, Florian; Di Cristanziano, Veronica; Lehmann, Helmar C. Journal: European journal of neurology Issue: Volume 29:Number 11(2022) Page Start: 3380 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Expanded Genetic Spectrum and Variable Disease Onset in AOPEP‐Associated Dystonia. Issue 5 (19th May 2022) Authors: Menden, Benita; Gutschalk, Alexander; Wunderlich, Gilbert; Haack, Tobias B. Journal: Movement disorders Issue: Volume 37:Issue 5(2022) Page Start: 1113 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease. Issue 4 (3rd March 2021) Authors: Keller, Natalie; Paketci, Cem; Altmueller, Janine; Fuhrmann, Nico; Wunderlich, Gilbert; Schrank, Bertold; Unver, Olcay; Yilmaz, Sanem; Boostani, Reza; Karimiani, Ehsan Ghayoor; Motameny, Susanne; Thiele, Holger; Nürnberg, Peter; Maroofian, Reza; Yis, Uluc; Wirth, Brunhilde; Karakaya, Mert Journal: Human mutation Issue: Volume 42:Issue 4(2021) Page Start: 460 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Lymphocyte antigens targetable by monoclonal antibodies in non-systemic vasculitic neuropathy. Issue 9 (26th May 2017) Authors: Schneider, Christian; Wunderlich, Gilbert; Bleistein, Johannes; Fink, Gereon R; Deckert, Martina; Brunn, Anna; Lehmann, Helmar Christoph Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 88:Issue 9(2017) Page Start: 756 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Motor unit number estimation in adult patients with spinal muscular atrophy treated with nusinersen. (20th July 2021) Authors: Schneider, Christian; Wassermann, Meike K.; Grether, Nicolai B.; Fink, Gereon R.; Wunderlich, Gilbert; Lehmann, Helmar C. Journal: European journal of neurology Issue: Volume 28:Number 9(2021) Page Start: 3022 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Nusinersen in adults with 5q spinal muscular atrophy: a non-interventional, multicentre, observational cohort study. Issue 4 (April 2020) Authors: Hagenacker, Tim; Wurster, Claudia D; Günther, René; Schreiber-Katz, Olivia; Osmanovic, Alma; Petri, Susanne; Weiler, Markus; Ziegler, Andreas; Kuttler, Josua; Koch, Jan C; Schneider, Ilka; Wunderlich, Gilbert; Schloss, Natalie; Lehmann, Helmar C; Cordts, Isabell; Deschauer, Marcus; Lingor, Paul; ... Journal: Lancet neurology Issue: Volume 19:Issue 4(2020) Page Start: 317 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Persistent hypokalaemia and intermittent muscle weakness. Issue 6 (30th July 2022) Authors: Rabenstein, Monika; Abicht, Angela; Brunn, Anna; Lehmann, Helmar; Wunderlich, Gilbert Journal: Practical neurology Issue: Volume 22:Issue 6(2022) Page Start: 518 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Rapid alterations in MR imaging in MELAS syndrome. Issue 5 (10th July 2019) Authors: Doppler, Christopher E J; Kabbasch, Christoph; Fink, Gereon R; Lehmann, Helmar C; Wunderlich, Gilbert Journal: Practical neurology Issue: Volume 19:Issue 5(2019) Page Start: 447 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Targeted sequencing with expanded gene profile enables high diagnostic yield in non‐5q‐spinal muscular atrophies. Issue 9 (25th July 2018) Authors: Karakaya, Mert; Storbeck, Markus; Strathmann, Eike A.; Delle Vedove, Andrea; Hölker, Irmgard; Altmueller, Janine; Naghiyeva, Leyla; Schmitz‐Steinkrüger, Lea; Vezyroglou, Katharina; Motameny, Susanne; Alawbathani, Salem; Thiele, Holger; Polat, Ayse Ipek; Okur, Derya; Boostani, Reza; Karimiani, Ehs... Journal: Human mutation Issue: Volume 39:Issue 9(2018) Page Start: 1284 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Transcript-Specific Loss-of-Function Variants in VPS16 Are Enriched in Patients With Dystonia. (7th February 2022) Authors: Park, Joohyun; Reilaender, Annemarie; Petry-Schmelzer, Jan N.; Stöbe, Petra; Cordts, Isabell; Harmuth, Florian; Rautenberg, Maren; Woerz, Sarah E.; Demidov, German; Sturm, Marc; Ossowski, Stephan; Schwaibold, Eva M.C.; Wunderlich, Gilbert; Paus, Sebastian; Saft, Carsten; Haack, Tobias B. Journal: Neurology Issue: Volume 8:Number 1(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗