- Contracturing granulomatous myositis in a patient with rheumatoid arthritis(2024)
Authors: Willem De Ridder, Laurens Van Herck, Gert Cypers, Isabelle Ravelingien, Jonathan Baets
Pages: 38 - 41
- Hereditary motor neuropathy(2024)
Authors: Jonathan De Winter, Jonathan Baets
Pages: 1 - 15
- Dominant NARS1 mutations causing axonal Charcot–Marie–Tooth disease expand NARS1 -associated diseases(2024)
Authors: Danique Beijer, Sheila Marte, Jiaxin C. Li, Willem De Ridder, Jessie Z. Chen, Abigail L.D. Tadenev, Kathy E. Miers, Tine Deconinck, Richard Macdonell, Wilson Marques, et al.
Pages: 1 - 9
- Overarching pathomechanisms in inherited peripheral neuropathies, spastic paraplegias, and cerebellar ataxias(2024)
Authors: Liedewei Van de Vondel, Jonathan De Winter, Vincent Timmerman, Jonathan Baets
Pages: 227 - 238
- Neuroinflammatory disease signatures in SPG11-related hereditary spastic paraplegia patients(2024)
Authors: Laura Krumm, Tatyana Pozner, Naime Zagha, Roland Coras, Philipp Arnold, Thanos Tsaktanis, Kathryn Scherpelz, Marie Y. Davis, Johanna Kaindl, Iris Stolzer, et al.
Pages: 1 - 25
- Myelin protein zero mutation-related hereditary neuropathies(2024)
Authors: Juliane Bremer, Axel Meinhardt, Istvan Katona, Jan Senderek, Elke K. Kaemmerer-Gassler, Andreas Roos, Andreas Ferbert, J. Michael Schroeder, Stefan Nikolin, Kay Nolte, et al.
Pages: 1 - 20
- C-terminal frameshift variant of TDP-₄₃ with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD(2023)
Authors: Pedro Ervilha Pereira, Nika Schuermans, Antoon Meylemans, Pontus LeBlanc, Lauren Versluys, Katie E.E. Copley, Jack D.D. Rubien, Christopher Altheimer, Myra Peetermans, Elke Debackere, et al.
Pages: 793 - 814
- Responsiveness of the scale for the assessment and rating of ataxia and natural history in 884 recessive and early onset ataxia patients(2023)
Authors: Andreas D. Traschuetz, Astrid Adarmes-Gomez, Mathieu Anheim, Jonathan Baets, Bernard Brais, Cynthia Gagnon, Janina Gburek-Augustat, Sarah Doss, Hasmet A. Hanagasi, Christoph Kamm, et al.
Pages: 470 - 485
- A homozygous loss of function variant in POPDC3(2023)
Authors: Willem De Ridder, Geert de Vries, Kristof Van Schil, Tine Deconinck, Vincent Mouly, Volker Straub, Jonathan Baets
Pages: 432 - 439
- Distinct features in adult polyglucosan body disease(2023)
Authors: Jonathan De Winter, Gert Cypers, Edwin Jacobs, Tine Deconinck, Willem De Ridder, Sven Dekeyzer, Jonathan Baets
Pages: 148 - 152