Publicaties
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Laboratoire de Neurologie KU Leuven
Anatomie comparée des mammifères domestiques, tome 7: neurologie, II: système nerveux périphérique ; glandes endocrines ; esthésiologie Universiteit Gent
Cognitive-motor Interference in Individuals With a Neurologic Disorder: A Systematic Review of Neural Correlates Universiteit Hasselt KU Leuven
Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders Universiteit Gent Universiteit Antwerpen
Background and Objectives : Owing to their extensive clinical and molecular heterogeneity, hereditary neurologic diseases in adults are difficult to diagnose. The current knowledge about the diagnostic yield and clinical utility of exome sequencing (ES) for neurologic diseases in adults is limited. This observational study assesses the diagnostic value of ES and multigene panel analysis in adult-onset neurologic disorders. Methods : From January ...
Early neurologic abnormalities associated with human T-cell lymphotropic virus type 1 infection in a cohort of Peruvian children Instituut voor Tropische Geneeskunde
The training and organization of Paediatric Neurology in Europe: Special report of the European Paediatric Neurology Society & Committee of National Advisors KU Leuven
BACKGROUND: Paediatric Neurology (PN) is a discipline focused on diagnosis, comprehensive management and research into diseases of the central and peripheral nervous system from fetal life to transition into adulthood. The European Paediatric Neurology Society first designed and published the European PN training programme in the European Paediatric Neurology Syllabus in 2002. This was important in gaining recognition for the sub-specialty from ...
Extremely elevated cerebrospinal fluid protein levels in a child with neurologic symptoms: beware of haemophagocytic lymphohistiocytosis KU Leuven Universiteit Antwerpen
Neurologic symptoms can be the initial manifestation of haemophagocytic lymphohistiocytosis (HLH). In this case study, we present a 3-year old boy with a clinical picture of encephalitis, a cerebrospinal fluid (CSF) protein level up to 1165 mg/dl and diffuse cerebral MRI abnormalities. The diagnosis of HLH was established only 6 weeks after initial presentation. The boy recovered after HLH therapy with persisting mild cognitive defects. Genetic ...