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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
111 - 120 of 176
- Autosomal dominant spinal muscular atrophy with lower extremity predominance: A recognizable phenotype of BICD2 mutations(2016)
Authors: Kristl Claeys
Pages: 496 - 500 - Novel genetic and neuropathological insights in neurogenic muscle weakness, ataxia, and retinitis pigmentosa (NARP)(2016)
Authors: Kristl Claeys
Pages: 328 - 333 - Expanded phenotypic spectrum of the m.8344A > G "MERRF" mutation: data from the German mitoNET registry(2016)
Authors: Kristl Claeys
Pages: 961 - 972 - Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?(2016)
Authors: Kristl Claeys
- Tubular aggregates in autoimmune Lambert-Eaton myasthenic syndrome(2016)
Authors: Kristl Claeys
Pages: 880 - 884 - Homozygosity for the common GAA gene splice site mutation c.-32-13T>G in Pompe disease is associated with the classical adult phenotypical spectrum(2015)
Authors: Kristl Claeys
Pages: 719 - 724 - Two novel nebulin variants in an adult patient with congenital nemaline myopathy(2015)
Authors: Kristl Claeys
Pages: 392 - 396 - Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathy(2015)
Authors: Kristl Claeys
Pages: 1346 - 1354 - Proteomic analysis in 72 myofibrillar myopathy (MFM) patients identifies new disease-relevant proteins accumulating in aggregates and reveals subtype-specific proteomic profiles(2014)
Authors: A Maerkens, M Olive, G Tasca, Kristl Claeys, R Barresi, A Sarkozy, G Pfeffer, T Evangelista, S Feldkirchner, J Reimann, et al.
Pages: 830 - 830 - Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies(2014)
Authors: Anna-Lena Semmler, Sabrina Sacconi, J Elisa Bach, Claus Liebe, Jan Buermann, Rudolf A Kley, Andreas Ferbert, Roland Anderheiden, Peter Van den Bergh, Jean-Jacques Martin, et al.