Cassiman D - Search Results

1

Tracer metabolomics reveals the role of aldose reductase in glycosylation.

Radenkovic S, Ligezka AN, Mokashi SS, Driesen K, Dukes-Rimsky L, Preston G, Owuocha LF, Sabbagh L, Mousa J, Lam C, Edmondson A, Larson A, Schultz M, Vermeersch P, Cassiman D, Witters P, Beamer LJ, Kozicz T, Flanagan-Steet H, Ghesquière B, Morava E. Radenkovic S, et al. Among authors: cassiman d. Cell Rep Med. 2023 Jun 20;4(6):101056. doi: 10.1016/j.xcrm.2023.101056. Epub 2023 May 30. Cell Rep Med. 2023. PMID: 37257447 Free PMC article.

2

Evaluation of the interference by homogentisic acid and other organic acids on the enzymatic and Jaffé method creatinine assay.

Pauwels S, Cassiman D, Vermeersch P. Pauwels S, et al. Among authors: cassiman d. Clin Chem Lab Med. 2012 Jan 6;50(4):749-50. doi: 10.1515/cclm.2011.836. Clin Chem Lab Med. 2012. PMID: 22505563 No abstract available.

3

Pregnancy during nitisinone treatment for tyrosinaemia type I: first human experience.

Vanclooster A, Devlieger R, Meersseman W, Spraul A, Kerckhove KV, Vermeersch P, Meulemans A, Allegaert K, Cassiman D. Vanclooster A, et al. Among authors: cassiman d. JIMD Rep. 2012;5:27-33. doi: 10.1007/8904_2011_88. Epub 2011 Dec 16. JIMD Rep. 2012. PMID: 23430914 Free PMC article.

4

Defining the phenotype and diagnostic considerations in adults with congenital disorders of N-linked glycosylation.

Wolthuis DF, Janssen MC, Cassiman D, Lefeber DJ, Morava E. Wolthuis DF, et al. Among authors: cassiman d. Expert Rev Mol Diagn. 2014 Mar;14(2):217-24. doi: 10.1586/14737159.2014.890052. Epub 2014 Feb 13. Expert Rev Mol Diagn. 2014. PMID: 24524732 Review.

5

ADAMTS5 deficiency protects against non-alcoholic steatohepatitis in obesity.

Bauters D, Spincemaille P, Geys L, Cassiman D, Vermeersch P, Bedossa P, Scroyen I, Lijnen HR. Bauters D, et al. Among authors: cassiman d. Liver Int. 2016 Dec;36(12):1848-1859. doi: 10.1111/liv.13181. Epub 2016 Jul 4. Liver Int. 2016. PMID: 27254774

6

Liver involvement in congenital disorders of glycosylation (CDG). A systematic review of the literature.

Marques-da-Silva D, Dos Reis Ferreira V, Monticelli M, Janeiro P, Videira PA, Witters P, Jaeken J, Cassiman D. Marques-da-Silva D, et al. Among authors: cassiman d. J Inherit Metab Dis. 2017 Mar;40(2):195-207. doi: 10.1007/s10545-016-0012-4. Epub 2017 Jan 20. J Inherit Metab Dis. 2017. PMID: 28108845 Review.

7

Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects.

Morelle W, Potelle S, Witters P, Wong S, Climer L, Lupashin V, Matthijs G, Gadomski T, Jaeken J, Cassiman D, Morava E, Foulquier F. Morelle W, et al. Among authors: cassiman d. J Clin Endocrinol Metab. 2017 Apr 1;102(4):1375-1386. doi: 10.1210/jc.2016-3443. J Clin Endocrinol Metab. 2017. PMID: 28323990 Free PMC article.

8

Nutritional Therapies in Congenital Disorders of Glycosylation (CDG).

Witters P, Cassiman D, Morava E. Witters P, et al. Among authors: cassiman d. Nutrients. 2017 Nov 7;9(11):1222. doi: 10.3390/nu9111222. Nutrients. 2017. PMID: 29112118 Free PMC article. Review.

9

Renal involvement in PMM2-CDG, a mini-review.

Altassan R, Witters P, Saifudeen Z, Quelhas D, Jaeken J, Levtchenko E, Cassiman D, Morava E. Altassan R, et al. Among authors: cassiman d. Mol Genet Metab. 2018 Mar;123(3):292-296. doi: 10.1016/j.ymgme.2017.11.012. Epub 2017 Nov 28. Mol Genet Metab. 2018. PMID: 29229467 Review.

10

Long-term outcome of transjugular intrahepatic portosystemic shunt for portal hypertension in autosomal recessive polycystic kidney disease.

Verbeeck S, Mekhali D, Cassiman D, Maleux G, Witters P. Verbeeck S, et al. Among authors: cassiman d. Dig Liver Dis. 2018 Jul;50(7):707-712. doi: 10.1016/j.dld.2018.03.009. Epub 2018 Mar 15. Dig Liver Dis. 2018. PMID: 29622386

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