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Page 1
Rhabdomyolysis in diabetic ketoacidosis.
Casteels K, Beckers D, Wouters C, Van Geet C. Casteels K, et al. Among authors: van geet c. Pediatr Diabetes. 2003 Mar;4(1):29-31. doi: 10.1034/j.1399-5448.2003.00026.x. Pediatr Diabetes. 2003. PMID: 14655521
Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12.
Goubau C, Devriendt K, Van der Aa N, Crepel A, Wieczorek D, Kleefstra T, Willemsen MH, Rauch A, Tzschach A, de Ravel T, Leemans P, Van Geet C, Buyse G, Freson K. Goubau C, et al. Among authors: van der aa n, van geet c. Eur J Hum Genet. 2013 Dec;21(12):1349-55. doi: 10.1038/ejhg.2013.86. Epub 2013 May 1. Eur J Hum Genet. 2013. PMID: 23632790 Free PMC article.
Functional studies and proteomics in platelets and fibroblasts reveal a lysosomal defect with increased cathepsin-dependent apoptosis in ATP1A3 defective alternating hemiplegia of childhood.
Di Michele M, Goubau C, Waelkens E, Thys C, De Vos R, Overbergh L, Schyns T, Buyse G, Casaer P, Van Geet C, Freson K. Di Michele M, et al. Among authors: van geet c. J Proteomics. 2013 Jun 28;86:53-69. doi: 10.1016/j.jprot.2013.05.005. Epub 2013 May 13. J Proteomics. 2013. PMID: 23681173
Unravelling the disease mechanism for TSPYL1 deficiency.
Buyse G, Di Michele M, Wijgaerts A, Louwette S, Wittevrongel C, Thys C, Downes K, Ceulemans B, Van Esch H, Van Geet C, Freson K. Buyse G, et al. Among authors: van esch h, van geet c. Hum Mol Genet. 2020 Dec 18;29(20):3431-3442. doi: 10.1093/hmg/ddaa233. Hum Mol Genet. 2020. PMID: 33075815 Free article.
Clinical practice: immune thrombocytopenia in paediatrics.
Labarque V, Van Geet C. Labarque V, et al. Among authors: van geet c. Eur J Pediatr. 2014 Feb;173(2):163-72. doi: 10.1007/s00431-013-2254-6. Epub 2014 Jan 5. Eur J Pediatr. 2014. PMID: 24390128 Review.
172 results