V. Goosens

Unraveling the Molecular Basis of the Dystrophic Process in Limb-Girdle Muscular Dystrophy LGMD-R12 by Differential Gene Expression Profiles in Diseased and Healthy Muscles

K. Claeys, R. Janky, D. Thal, 2022, Cells.

Clinical and muscle MRI features in a family with tubular aggregate myopathy and novel STIM1 mutation

K. Claeys, T. Theys, V. Racé, 2020, Neuromuscular Disorders.

Nusinersen treatment significantly improves hand grip strength, hand motor function and MRC sum scores in adult patients with spinal muscular atrophy types 3 and 4

K. Claeys, K. Claes, V. Goosens, 2020, Journal of Neurology.

Longitudinal cortical split sign as a potential diagnostic feature for cortical osteitis.

F. Vanhoenacker, P. Brys, I. Samson, 2010, JBR-BTR : organe de la Societe royale belge de radiologie (SRBR) = orgaan van de Koninklijke Belgische Vereniging voor Radiologie.

Whole‐body muscle magnetic resonance imaging in patients with muscle symptoms: incidental findings and outcomes

K. Claeys, V. Goosens, 2020, European journal of neurology.

Vallecular cyst as a cause of congenital stridor: report of five patients

L. Breysem, M. Proesmans, V. Vander Poorten, 2009, Pediatric Radiology.

Histopathological correlations and fat replacement imaging patterns in recessive limb‐girdle muscular dystrophy type 12

P. Dupont, K. Claeys, D. Thal, 2023, Journal of cachexia, sarcopenia and muscle.