< Back to previous page
Researcher
Kristl Claeys
- Disciplines:Neurosciences, Biological and physiological psychology, Cognitive science and intelligent systems, Developmental psychology and ageing
Affiliations
- Laboratory for Muscle Diseases and Neuropathies (Lab)
Responsible
From1 Dec 2016 → Today - Laboratory for Muscle Diseases and Neuropathies (Lab)
Member
From1 Dec 2016 → Today - Research Group Experimental Neurology (Division)
Member
From1 Jan 2016 → 30 Nov 2016
Projects
1 - 6 of 6
- Engelstalig: precision medicine en care in patients neuromuscular dystrophyFrom1 Oct 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Evaluating novel radiological and clinical outcome measures in hereditary neuromuscular diseases.From1 Jun 2022 → TodayFunding: Own budget, for example: patrimony, inscription fees, gifts
- Mass spectrometry-based autoantibody tests for specific diagnosis of autoimmune diseasesFrom1 Oct 2020 → 30 Sep 2022Funding: IOF - technology validation in lab
- TOWARDS TRIAL READINESS IN HEREDITARY NEUROMUSCULAR DISEASES: Developing accurate, feasible and non-invasive outcome measures.From1 Oct 2019 → 1 Oct 2023Funding: FWO fellowships
- Immune profiling of neurological diseases (IPoN)From1 Aug 2018 → 1 Oct 2023Funding: FWO fellowships
- A comprehensive study of genetic determinants of motor neuron vulnerabilityFrom1 Oct 2017 → 2 May 2022Funding: FWO fellowships
Publications
21 - 30 of 176
- A retrospective survey of patients with hereditary transthyretin-mediated (hATTR) amyloidosis treated with patisiran in real-world clinical practice in Belgium(2023)
Authors: Kristl Claeys
Pages: 1029 - 1037 - Histopathological correlations and fat replacement imaging patterns in recessive limb-girdle muscular dystrophy type 12(2023)
Authors: Bram De Wel, Lotte Huysmans, Christophe Depuydt, Ronald Peeters, Dietmar Thal, Patrick Dupont, Frederik Maes, Kristl Claeys
Pages: 1468 - 1481 - Automated MRI quantification of volumetric per-muscle fat fractions in the proximal leg of patients with muscular dystrophies(2023)
Authors: Lotte Huysmans, Bram De Wel, Kristl Claeys, Frederik Maes
- Mass spectrometry-based identification of new anti-Ly and known antisynthetase autoantibodies(2023)
Authors: Jean-Baptiste Vulsteke, Rita Derua, Petra De Haes, Daniel Engelbert Blockmans, Wim Wuyts, Kristl Claeys, Ellen De Langhe, Xavier Bossuyt
Pages: 546 - 555 - Validation of an Artificial Intelligence driven framework to automatically detect red flag symptoms in screening for rare diseases in electronic health records: hereditary transthyretin amyloidosis polyneuropathy as a key example(2023)
Authors: Kristl Claeys
Pages: 79 - 85 - Author Response: Prospective Natural History Study in 24 Adult Patients With LGMDR12 Over 2 Years of Follow-up: Quantitative MRI and Clinical Outcome Measures(2023)
Authors: Bram De Wel, Kristl Claeys
Pages: 354 - 354 - Author Response: Prospective Natural History Study in 24 Adult Patients With LGMDR12 Over 2 Years of Follow-up: Quantitative MRI and Clinical Outcome Measures(2023)
Authors: Bram De Wel, Kristl Claeys
Pages: 354 - 354 - Identification of new telomere- and telomerase-associated autoantigens in systemic sclerosis(2023)
Authors: Jean-Baptiste Vulsteke, Rita Derua, Daniel Engelbert Blockmans, Petra De Haes, Steven Vanderschueren, Kristl Claeys, Wim Wuyts, Patrick Verschueren, Ellen De Langhe, Xavier Bossuyt
- Telemedicine in Neuromuscular Diseases During Covid-19 Pandemic: ERN-NMD European Survey(2023)
Authors: Kristl Claeys
Pages: 173 - 184 - NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy(2022)
Authors: Kristl Claeys