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Page 1
[Are we genetically predisposed to addictions?].
Castermans E, Gaillez S, Bours V. Castermans E, et al. Among authors: gaillez s. Rev Med Liege. 2013 May-Jun;68(5-6):226-32. Rev Med Liege. 2013. PMID: 23888569 Free article. French.
[X-linked hydrocephaly. A case report in fetal medicine].
Syrios K, Delbecoue K, Gaillez S, Schaaps JP, Chantraine F. Syrios K, et al. Among authors: gaillez s. Rev Med Liege. 2011 Mar;66(3):126-9. Rev Med Liege. 2011. PMID: 21560427 Free article. French.
Diagnostic pitfall in antenatal manifestations of CPT II deficiency.
Boemer F, Deberg M, Schoos R, Caberg JH, Gaillez S, Dugauquier C, Delbecque K, François A, Maton P, Demonceau N, Senterre G, Ferdinandusse S, Debray FG. Boemer F, et al. Among authors: gaillez s. Clin Genet. 2016 Feb;89(2):193-7. doi: 10.1111/cge.12593. Epub 2015 May 5. Clin Genet. 2016. PMID: 25827434
Pseudo-Bartter syndrome in a pregnant mother and her fetus.
Mathot M, Maton P, Henrion E, François-Adant A, Marguglio A, Gaillez S, Collard L, Langhendries JP. Mathot M, et al. Among authors: gaillez s. Pediatr Nephrol. 2006 Jul;21(7):1037-40. doi: 10.1007/s00467-006-0123-5. Epub 2006 May 30. Pediatr Nephrol. 2006. PMID: 16773420
Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.
Vanakker O, Vilain C, Janssens K, Van der Aa N, Smits G, Bandelier C, Blaumeiser B, Bulk S, Caberg JH, De Leener A, De Rademaeker M, de Ravel T, Desir J, Destree A, Dheedene A, Gaillez S, Grisart B, Hellin AC, Janssens S, Keymolen K, Menten B, Pichon B, Ravoet M, Revencu N, Rombout S, Staessens C, Van Den Bogaert A, Van Den Bogaert K, Vermeesch JR, Kooy F, Sznajer Y, Devriendt K. Vanakker O, et al. Among authors: gaillez s. Eur J Med Genet. 2014 Mar;57(4):151-6. doi: 10.1016/j.ejmg.2014.02.002. Epub 2014 Feb 15. Eur J Med Genet. 2014. PMID: 24534801 Review.
11 results