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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 dystrophyFrom7 Nov 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
101 - 110 of 171
- Clinical and biometrical 12-month follow-up in patients after reconstruction of the sural nerve biopsy defect by the collagen-based nerve guide Neuromaix(2017)
Authors: Kristl Claeys
Pages: 34 - 46 - Improving genetic diagnosis in Mendelian disease with transcriptome sequencing(2017)
Authors: Kristl Claeys
Pages: 1 - 11 - Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus-Associated Guillain-Barré Syndrome(2017)
Authors: Kristl Claeys, Koen Poesen, Philip Van Damme
Pages: 26 - 33 - Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases(2017)
Authors: Philip Van Damme, Thomas Tousseyn, Dietmar Thal, Kristl Claeys
Pages: 86 - 98 - Anterior interosseous mononeuropathy associated with HEV infection(2017)
Authors: Bart Swinnen, Steven Boeynaems, Maarten Schrooten, Kristl Claeys, Philip Van Damme
- 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