de Vroede MA - Search Results

1

Fetal sex determination from maternal plasma in pregnancies at risk for congenital adrenal hyperplasia.

Rijnders RJ, van der Schoot CE, Bossers B, de Vroede MA, Christiaens GC. Rijnders RJ, et al. Among authors: de vroede ma. Obstet Gynecol. 2001 Sep;98(3):374-8. doi: 10.1016/s0029-7844(01)01480-6. Obstet Gynecol. 2001. PMID: 11530115

2

[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. Among authors: de vroede ma. Ned Tijdschr Geneeskd. 2005 May 21;149(21):1156-8. Ned Tijdschr Geneeskd. 2005. PMID: 15940919 Review. Dutch.

3

A special case of congenital adrenal hypoplasia and acute bilateral infantile striatal necrosis.

van der Ent CK, de Vroede MA, Augustijn PB, Wit JM. van der Ent CK, et al. Among authors: de vroede ma. Acta Paediatr. 1995 Aug;84(8):957-60. doi: 10.1111/j.1651-2227.1995.tb13805.x. Acta Paediatr. 1995. PMID: 7488830

4

Rectal hydrocortisone during stress in patients with adrenal insufficiency.

De Vroede M, Beukering R, Spit M, Jansen M. De Vroede M, et al. Arch Dis Child. 1998 Jun;78(6):544-7. doi: 10.1136/adc.78.6.544. Arch Dis Child. 1998. PMID: 9713011 Free PMC article.

5

Short stature as the only presenting feature in a patient with an isodicentric (Y)(q11.23) and gonadoblastoma. A clinical and molecular cytogenetic study.

Giltay JC, Ausems MG, van Seumeren I, Zewald RA, Sinke RJ, Faas B, de Vroede M. Giltay JC, et al. Eur J Pediatr. 2001 Mar;160(3):154-8. doi: 10.1007/s004310000683. Eur J Pediatr. 2001. PMID: 11277375

6

Cardiovascular and metabolic outcome in 6-8 year old offspring of women with type 1 diabetes with near-optimal glycaemic control during pregnancy.

Rijpert M, Evers IM, de Valk HW, de Vroede MA, Tersteeg-Kamperman M, Heijnen CJ, Visser GH. Rijpert M, et al. Among authors: de vroede ma. Early Hum Dev. 2011 Jan;87(1):49-54. doi: 10.1016/j.earlhumdev.2010.10.002. Epub 2010 Nov 20. Early Hum Dev. 2011. PMID: 21095079

7

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. Among authors: de vroede ma. 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

8

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. Among authors: de vroede ma. Diabetes Metab Res Rev. 2012 Sep;28(6):527-34. doi: 10.1002/dmrr.2306. Diabetes Metab Res Rev. 2012. PMID: 22492505

9

[Follow-up of adult women with Turner's syndrome in a cohort study in Utrecht].

Broekhuijsen-van Henten DM, de Vroede M. Broekhuijsen-van Henten DM, et al. Ned Tijdschr Geneeskd. 2007 Jul 21;151(29):1630-4. Ned Tijdschr Geneeskd. 2007. PMID: 17727185 Dutch.

10

[When is a tall child too tall?].

Breukels MA, de Vroede MA. Breukels MA, et al. Among authors: de vroede ma. Ned Tijdschr Geneeskd. 2005 May 7;149(19):1021-4. Ned Tijdschr Geneeskd. 2005. PMID: 15909388 Dutch.

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