Our main subject is thyroid disease in children, but we are also interested in all endocrine diseases in children, such as cortisol deficiency or type 1 diabetes:

  • Samuels ME, Gallo-Payet N, Pinard S, Hasselman C, Magne F, Patry L, Chouinard L, Schwartzentruber J, René P, Sawyer N, Bouvier M, Djemli A, Delvin E, Huot C, Eugene D,Deal CL Van Vliet G, Majewski J, Deladoëy J. Bioinactive ACTH Causing Glucocorticoid Deficiency. J Clin Endocrinol Metab 2013; 98: 736-742. Highlighted by an article in lay journal La Presse (31 January 2013), the main French daily journal of the city of Montreal. Interview for Radio-Canada International (6 February 2013)
  • Wildi-Runge S*, Deladoëy J*, Bélanger C, Deal CL, Van Vliet G, Alos N, Huot C. A search for variables predicting cortisol response to low dose cortricotropin stimulation following supraphysiological doses of glucocorticoids. (*co-1st author) J Pediatr 2013 (Epub 12 Feb 2013)
  • Hasselmann C*, Deladoëy J*, Vuissoz JM, Patry JM, Alirezaie N, Schwartzentruber J, Deal CL, Van Vliet G, Majewski J, Samuels M. Expanding the phenotypic spectrum of nicotinamide nucleotide transhydrogenase(NNT) mutations and using whole exome sequencing to discover potential disease modifiers. (*co-1st author) J Genomes Exomes 2013; 1: 19-30 (doi: 10.4137/JGE.S11378); open access at http://www.la-press.com
  • Deladoëy J and Van Vliet G. Treating Congenital Hypothyroidism: which levothyroxine? Nat Rev Endocrinol 2013 (Epub 5 March 2013)
  • Deladoëy J, Henderson M, Geoffroy L. Linear association between household income and metabolic control in children with insulin-dependent diabetes mellitus despite free access to health care. J Clin Endocrinol Metab 2013 (Epub 28 March).Highlighted by an article in lay journal The Gazette (4 April 2013), the main English daily journal of the city of Montreal
  • Sharkia M, Michaud S, Berthier MT, Giguère Y, Stewart L, Deladoëy J, Deal CL, Van Vliet G, Chanoine JP. Thyroid function from birth to adolescence in Prader-Willi Syndrome. J Pediatr 2013 (Epub 29 April 2013)
  • Grob F, Deladoëy J, Legault L, Spigelblatt L, Fournier A, Parma J, Vassart G, Van Vliet G. Autonomous adenomas caused by somatic mutations of the thyrotropin receptor in children. Horm Res Ped  2014;  81 :73-79.
  • Abu-Khudir R, Magne F, Chanoine JP, Deal C, Van Vliet G, Deladoëy J. Role for tissue-dependent methylation differences in the expression of FOXE1 in non-tumoral thyroid glands. J Clin Endocrinol Metab 2014; 99(6): E1120-E1129.
  • Deladoëy J, Van Vliet G. The changing epidemiology of congenital hypothyroidism: fact or artifact? Expert Review in Endocrinology 2014; 9(4): 387-395.
  • Magne F, Serpa R, Van Vliet G, Samuels ME, Deladoëy J. Somatic mutations are not observed by exome sequencing of lymphocyte DNA from monozygotic twins discordant for congenital hypothyroidism with thyroid dysgenesis. Horm Res Ped 2014; Epub 2014 Sep 23; (DOI: 10.1159/000365393. Open access link : http://www.karger.com/DOI/10.1159/000365393).
  • Opitz R*, Hitz MP*, Vandernoot I, Trubiroha A, Abu-Khudir R, Samuels M, Désilets V, Costagliola S*, Andelfinger G*, Deladoëy J*. Functional Zebrafish Studies Based on Human Genotyping Point to Netrin-1 as a Link between Aberrant Cardiovascular Development and Thyroid Dysgenesis. (* equal contributors) Endocrinology 2015; 156(1): 377-388. (* equal contributors)
  • Van Vliet G*, Deladoëy J*. Sublingual thyroid ectopy: similarities and differences with Kallmann Syndrome. (* equal contributors) F1000 Prime Rep 2015, 7:20. http://f1000.com/prime/reports/m/7/20
  • Decaussin-Petrucci M, Sassolas G, Hafdi-Nejjari Z, Borson-Chazot F, Abu-Khudir R, Deladoëy J, Cournoyer S, Sartelet H. Expression of CD 133 in differentiated thyroid cancer of young patients. J Clin Pathol 2015 ; Epub 2015 March 13 (doi:10.1136/jclinpath-2014-202625)