Jonathan Baets, Ph.D.
Affiliations: | 2011 | Universiteit Antwerpen (Belgium) |
Area:
Medicine and Surgery, Genetics, Neuroscience BiologyGoogle:
"Jonathan Baets"Mean distance: 35622
Parents
Sign in to add mentor| Paul Parizel | grad student | 2011 | Universiteit Antwerpen (Belgium) | |
| (Genotype phenotype correlations in hereditary neuropathies: A systematic approach.) | ||||
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Publications
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| Beijer D, Marte S, Li JC, et al. (2024) Dominant mutations causing axonal Charcot-Marie-Tooth disease expand -associated diseases. Brain Communications. 6: fcae070 |
| Van de Vondel L, De Winter J, Timmerman V, et al. (2024) Overarching pathomechanisms in inherited peripheral neuropathies, spastic paraplegias, and cerebellar ataxias. Trends in Neurosciences. 47: 227-238 |
| Lischka A, Eggermann K, Record CJ, et al. (2023) Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathies. Brain : a Journal of Neurology |
| Ervilha Pereira P, Schuermans N, Meylemans A, et al. (2023) C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD. Acta Neuropathologica |
| De Bleecker JL, Claeys KG, Delstanche S, et al. (2023) A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium. Acta Neurologica Belgica |
| Malcorps M, Amor-Barris S, Burnyte B, et al. (2022) HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling. Orphanet Journal of Rare Diseases. 17: 374 |
| Van de Vondel L, De Winter J, Beijer D, et al. (2022) De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia. Movement Disorders : Official Journal of the Movement Disorder Society |
| Longo F, De Ritis D, Miluzio A, et al. (2021) Assessment of Sacsin Turnover in Patients With ARSACS: Implications for Molecular Diagnosis and Pathogenesis. Neurology |
| Beijer D, Agnew T, Rack JGM, et al. (2021) Biallelic mutations in complex neuropathy affect ADP ribosylation and DNA damage response. Life Science Alliance. 4 |
| Beijer D, Kim HJ, Guo L, et al. (2021) Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation. Jci Insight. 6 |