prof. dr. Jan De Bleecker
work address
De Pintelaan 185, 1K12-IA
9000 Gent
9000 Gent
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- 2017
- TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis
- 2016
- Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis
- Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups
- 213th ENMC international workshop: Outcome measures and clinical trial readiness in idiopathic inflammatory myopathies, Heemskerk, The Netherlands, 18-20 September 2015
- Comprehensive analysis of TTN coding regions in myopathic patients: challenges and opportunities
- Database crossing allows better understanding of neuromuscular disorders epidemiology: the Belgian example
- Activation of osmolyte pathways in inflammatory myopathy and Duchenne muscular dystrophy points to osmoregulation as a contributing pathogenic mechanism
- The genetic basis of undiagnosed muscular dystrophies and myopathies: results from 504 patients
- En de 'khat' komt weer...: recidief van een ischemisch cerebraal infarct bij een jongeman
- NFAT5 in Duchenne muscular dystrophy cultured myoblasts after exposure to hyperosmolar salt conditions