- Work address
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Neurologie C. Heymanslaan 10
9000 Gent - Dimitri.Hemelsoet@UGent.be
- ORCID iD
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0000-0001-5403-3092
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- Journal Article
- A1
- open access
Shortcutting the diagnostic odyssey : the multidisciplinary program for undiagnosed rare diseases in adults (UD-PrOZA)
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- Journal Article
- A1
- open access
Mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF, and result in Aicardi-Goutières syndrome with severe end-organ involvement
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Clinical and subclinical findings in heterozygous ABCC6 carriers : results from a Belgian cohort and clinical practice guidelines
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Is monitoring of antiplatelet therapy by light transmission aggregometry dependent on instrument and reagent used?
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Alemtuzumab in multiple sclerosis : a retrospective analysis of occult hemorrhagic magnetic resonance imaging lesions and risk factors
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Novel mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF and result in Aicardi-Goutières syndrome with severe end-organ involvement
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Microbleed patterns in critical illness and COVID-19
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Dysarthria following acute ischemic stroke : prospective evaluation of characteristics, type and severity
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The feasibility, usability and acceptability of a tablet-based aphasia therapy in the acute phase following stroke
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Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation