prof. dr. Jan De Bleecker
- Work address
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C. Heymanslaan 10, ingang 12 - verdieping 12
9000 Gent - Jan.DeBleecker@UGent.be
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- Journal Article
- A1
- open access
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone‐rod dystrophy, hearing loss and reduced male fertility
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Multisystem proteinopathy due to a homozygous p.Arg159His VCP mutation : a tale of the unexpected
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The myokine GDF-15 is a potential biomarker for myositis and associates with the protein aggregates of sporadic inclusion body myositis.
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Expansion of the role and functional characterization of a missense variant in CEP78 associated with cone-rod dystrophy and hearing loss
(2019) -
Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy
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Current evidence for treatment with nusinersen for spinal muscular atrophy : a systematic review
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Safety and efficacy of intravenous bimagrumab in inclusion body myositis (RESILIENT) : a randomised, double-blind, placebo-controlled phase 2b trial
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A phase 3 multicenter, prospective, open-label efficacy and safety study of immune globulin (human) 10% caprylate/chromatography purified in patients with myasthenia gravis exacerbations
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- Journal Article
- A1
- open access
Long-term efficacy and safety of eculizumab in Japanese patients with generalized myasthenia gravis : a subgroup analysis of the REGAIN open-label extension study
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Idiopathic inflammatory myopathy : interrater variability in muscle biopsy reading