Verrijn Stuart AA - Search Results

1

[From gene to disease; congenital adrenal hypoplasia and the DAX-1 gene].

Verrijn Stuart AA, de Vroede MA, Giltay JC. Verrijn Stuart AA, et al. Ned Tijdschr Geneeskd. 2005 May 21;149(21):1156-8. Ned Tijdschr Geneeskd. 2005. PMID: 15940919 Review. Dutch.

2

An amino-terminal DAX1 (NROB1) missense mutation associated with isolated mineralocorticoid deficiency.

Verrijn Stuart AA, Ozisik G, de Vroede MA, Giltay JC, Sinke RJ, Peterson TJ, Harris RM, Weiss J, Jameson JL. Verrijn Stuart AA, et al. J Clin Endocrinol Metab. 2007 Mar;92(3):755-61. doi: 10.1210/jc.2005-2429. Epub 2006 Dec 12. J Clin Endocrinol Metab. 2007. PMID: 17164309

3

Recognition of heat shock protein 60 epitopes in children with type 1 diabetes.

Verrijn Stuart AA, de Jager W, Klein MR, Teklenburg G, Nuboer R, Hoorweg JJ, de Vroede MA, de Kruijff I, Fick M, Schroor EJ, van der Vlist GJ, Meerding J, Kamphuis S, Prakken BJ. Verrijn Stuart AA, et al. Diabetes Metab Res Rev. 2012 Sep;28(6):527-34. doi: 10.1002/dmrr.2306. Diabetes Metab Res Rev. 2012. PMID: 22492505

4

Familial Male-limited Precocious Puberty (FMPP) and Testicular Germ Cell Tumors.

Kooij CD, Mavinkurve-Groothuis AMC, Kremer Hovinga ICL, Looijenga LHJ, Rinne T, Giltay JC, de Kort LMO, Klijn AJ, de Krijger RR, Verrijn Stuart AA. Kooij CD, et al. Among authors: verrijn stuart aa. J Clin Endocrinol Metab. 2022 Nov 23;107(11):3035-3044. doi: 10.1210/clinem/dgac516. J Clin Endocrinol Metab. 2022. PMID: 36071555 Free PMC article. Review.

5

[From gene to disease; hypophosphataemic rickets and the PHEX gene].

Jansen M, van Dael CM, Verrijn Stuart AA, van der Hout AH, Rump P. Jansen M, et al. Among authors: verrijn stuart aa. Ned Tijdschr Geneeskd. 2006 Jun 24;150(25):1390-4. Ned Tijdschr Geneeskd. 2006. PMID: 16841587 Review. Dutch.

6

Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2-->qter.

Poot M, Eleveld MJ, van 't Slot R, van Genderen MM, Verrijn Stuart AA, Hochstenbach R, Beemer FA. Poot M, et al. Among authors: verrijn stuart aa. Eur J Med Genet. 2007 Nov-Dec;50(6):432-40. doi: 10.1016/j.ejmg.2007.08.003. Epub 2007 Sep 9. Eur J Med Genet. 2007. PMID: 17931990

7

Variable behavioural phenotypes of patients with monosomies of 15q26 and a review of 16 cases.

Poot M, Verrijn Stuart AA, van Daalen E, van Iperen A, van Binsbergen E, Hochstenbach R. Poot M, et al. Among authors: verrijn stuart aa. Eur J Med Genet. 2013 Jul;56(7):346-50. doi: 10.1016/j.ejmg.2013.04.001. Epub 2013 Apr 16. Eur J Med Genet. 2013. PMID: 23603061 Review.

8

Altered plasma adipokine levels and in vitro adipocyte differentiation in pediatric type 1 diabetes.

Verrijn Stuart AA, Schipper HS, Tasdelen I, Egan DA, Prakken BJ, Kalkhoven E, de Jager W. Verrijn Stuart AA, et al. J Clin Endocrinol Metab. 2012 Feb;97(2):463-72. doi: 10.1210/jc.2011-1858. Epub 2011 Nov 23. J Clin Endocrinol Metab. 2012. PMID: 22112811

9

Serum Cytokines as Biomarkers in Islet Cell Transplantation for Type 1 Diabetes.

van der Torren CR, Verrijn Stuart AA, Lee D, Meerding J, van de Velde U, Pipeleers D, Gillard P, Keymeulen B, de Jager W, Roep BO. van der Torren CR, et al. Among authors: verrijn stuart aa. PLoS One. 2016 Jan 11;11(1):e0146649. doi: 10.1371/journal.pone.0146649. eCollection 2016. PLoS One. 2016. PMID: 26751709 Free PMC article.

10

Vitamin D deficiency in childhood obesity is associated with high levels of circulating inflammatory mediators, and low insulin sensitivity.

Reyman M, Verrijn Stuart AA, van Summeren M, Rakhshandehroo M, Nuboer R, de Boer FK, van den Ham HJ, Kalkhoven E, Prakken B, Schipper HS. Reyman M, et al. Among authors: verrijn stuart aa. Int J Obes (Lond). 2014 Jan;38(1):46-52. doi: 10.1038/ijo.2013.75. Epub 2013 May 20. Int J Obes (Lond). 2014. PMID: 23736361

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