Van Vliet G - Search Results

1

Conserved Telomere Length in Human Ectopic Thyroids: An Argument Against Premature Differentiation Causing Arrested Migration.

Larrivée-Vanier S, Magne F, Patey N, Chanoine JP, Vuissoz JM, Van Vliet G, Deladoëy J. Larrivée-Vanier S, et al. Among authors: van vliet g. Thyroid. 2015 Sep;25(9):1050-4. doi: 10.1089/thy.2015.0204. Epub 2015 Aug 3. Thyroid. 2015. PMID: 26131731 Free PMC article.

2

Variation by ethnicity in the prevalence of congenital hypothyroidism due to thyroid dysgenesis.

Stoppa-Vaucher S, Van Vliet G, Deladoëy J. Stoppa-Vaucher S, et al. Among authors: van vliet g. Thyroid. 2011 Jan;21(1):13-8. doi: 10.1089/thy.2010.0205. Epub 2010 Nov 8. Thyroid. 2011. PMID: 21054242 Free PMC article.

3

Demonstration of Autosomal Monoallelic Expression in Thyroid Tissue Assessed by Whole-Exome and Bulk RNA Sequencing.

Magne F, Ge B, Larrivée-Vanier S, Van Vliet G, Samuels ME, Pastinen T, Deladoëy J. Magne F, et al. Among authors: van vliet g. Thyroid. 2016 Jun;26(6):852-9. doi: 10.1089/thy.2016.0009. Epub 2016 May 18. Thyroid. 2016. PMID: 27125219

4

Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism.

Dufort G, Larrivée-Vanier S, Eugène D, De Deken X, Seebauer B, Heinimann K, Lévesque S, Gravel S, Szinnai G, Van Vliet G, Deladoëy J. Dufort G, et al. Among authors: van vliet g. Thyroid. 2019 Jul;29(7):1018-1022. doi: 10.1089/thy.2018.0461. Epub 2019 May 31. Thyroid. 2019. PMID: 31030636

5

Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.

Larrivée-Vanier S, Jean-Louis M, Magne F, Bui H, Rouleau GA, Spiegelman D, Samuels ME, Kibar Z, Van Vliet G, Deladoëy J. Larrivée-Vanier S, et al. Among authors: van vliet g. Thyroid. 2022 May;32(5):486-495. doi: 10.1089/thy.2021.0597. Epub 2022 Apr 25. Thyroid. 2022. PMID: 35272499 Free PMC article.

6

Random variability in congenital hypothyroidism from thyroid dysgenesis over 16 years in Québec.

Deladoëy J, Bélanger N, Van Vliet G. Deladoëy J, et al. Among authors: van vliet g. J Clin Endocrinol Metab. 2007 Aug;92(8):3158-61. doi: 10.1210/jc.2007-0527. Epub 2007 May 15. J Clin Endocrinol Metab. 2007. PMID: 17504897

7

Possible non-Mendelian mechanisms of thyroid dysgenesis.

Deladoëy J, Vassart G, Van Vliet G. Deladoëy J, et al. Among authors: van vliet g. Endocr Dev. 2007;10:29-42. doi: 10.1159/000106818. Endocr Dev. 2007. PMID: 17684388 Review.

8

Pseudodominant inheritance of goitrous congenital hypothyroidism caused by TPO mutations: molecular and in silico studies.

Deladoëy J, Pfarr N, Vuissoz JM, Parma J, Vassart G, Biesterfeld S, Pohlenz J, Van Vliet G. Deladoëy J, et al. Among authors: van vliet g. J Clin Endocrinol Metab. 2008 Feb;93(2):627-33. doi: 10.1210/jc.2007-2276. Epub 2007 Nov 20. J Clin Endocrinol Metab. 2008. PMID: 18029453

9

A high prevalence of dual thyroid ectopy in congenital hypothyroidism: evidence for insufficient signaling gradients during embryonic thyroid migration or for the polyclonal nature of the thyroid gland?

Wildi-Runge S, Stoppa-Vaucher S, Lambert R, Turpin S, Van Vliet G, Deladoëy J. Wildi-Runge S, et al. Among authors: van vliet g. J Clin Endocrinol Metab. 2012 Jun;97(6):E978-81. doi: 10.1210/jc.2011-3156. Epub 2012 Mar 28. J Clin Endocrinol Metab. 2012. PMID: 22456623

10

Thyroid function from birth to adolescence in Prader-Willi syndrome.

Sharkia M, Michaud S, Berthier MT, Giguère Y, Stewart L, Deladoëy J, Deal C, Van Vliet G, Chanoine JP. Sharkia M, et al. Among authors: van vliet g. J Pediatr. 2013 Sep;163(3):800-5. doi: 10.1016/j.jpeds.2013.03.058. Epub 2013 Apr 25. J Pediatr. 2013. PMID: 23623517

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