Pajkrt E - Search Results

1

NIPT-based screening for Down syndrome and beyond: what do pregnant women think?

van Schendel RV, Dondorp WJ, Timmermans DR, van Hugte EJ, de Boer A, Pajkrt E, Lachmeijer AM, Henneman L. van Schendel RV, et al. Among authors: pajkrt e. Prenat Diagn. 2015 Jun;35(6):598-604. doi: 10.1002/pd.4579. Epub 2015 Mar 30. Prenat Diagn. 2015. PMID: 25693726

2

Screening for Down's syndrome by fetal nuchal translucency measurement in a general obstetric population.

Pajkrt E, van Lith JM, Mol BW, Bleker OP, Bilardo CM. Pajkrt E, et al. Ultrasound Obstet Gynecol. 1998 Sep;12(3):163-9. doi: 10.1046/j.1469-0705.1998.12030163.x. Ultrasound Obstet Gynecol. 1998. PMID: 9793187 Free article. Clinical Trial.

3

Early pregnancy screening for fetal aneuploidy with serum markers and nuchal translucency.

de Graaf IM, Pajkrt E, Bilardo CM, Leschot NJ, Cuckle HS, van Lith JM. de Graaf IM, et al. Among authors: pajkrt e. Prenat Diagn. 1999 May;19(5):458-62. doi: 10.1002/(sici)1097-0223(199905)19:5<458::aid-pd569>3.0.co;2-a. Prenat Diagn. 1999. PMID: 10360515

4

Use of the disutility ratio in prenatal screening for Down's syndrome.

van der Meulen JH, Mol BW, Pajkrt E, van Lith JM, Voorn W. van der Meulen JH, et al. Among authors: pajkrt e. Br J Obstet Gynaecol. 1999 Feb;106(2):108-15. doi: 10.1111/j.1471-0528.1999.tb08209.x. Br J Obstet Gynaecol. 1999. PMID: 10426675

5

Co-variables in first trimester maternal serum screening.

de Graaf IM, Cuckle HS, Pajkrt E, Leschot NJ, Bleker OP, van Lith JM. de Graaf IM, et al. Among authors: pajkrt e. Prenat Diagn. 2000 Mar;20(3):186-9. Prenat Diagn. 2000. PMID: 10719318

6

Fetal genital anomalies: an aid to diagnosis.

Pajkrt E, Petersen OB, Chitty LS. Pajkrt E, et al. Prenat Diagn. 2008 May;28(5):389-98. doi: 10.1002/pd.1979. Prenat Diagn. 2008. PMID: 18395878

7

Brachmann-de Lange syndrome: definition of prenatal sonographic features to facilitate definitive prenatal diagnosis.

Pajkrt E, Griffin DR, Chitty LS. Pajkrt E, et al. Prenat Diagn. 2010 Sep;30(9):865-72. doi: 10.1002/pd.2577. Prenat Diagn. 2010. PMID: 20665529

8

Targeted ultrasound examination and DNA testing for Noonan syndrome, in fetuses with increased nuchal translucency and normal karyotype.

Bakker M, Pajkrt E, Mathijssen IB, Bilardo CM. Bakker M, et al. Among authors: pajkrt e. Prenat Diagn. 2011 Sep;31(9):833-40. doi: 10.1002/pd.2782. Epub 2011 Jun 27. Prenat Diagn. 2011. PMID: 21706501 Review.

9

Fetal forearm anomalies: prenatal diagnosis, associations and management strategy.

Pajkrt E, Cicero S, Griffin DR, van Maarle MC, Chitty LS. Pajkrt E, et al. Prenat Diagn. 2012 Nov;32(11):1084-93. doi: 10.1002/pd.3962. Epub 2012 Aug 18. Prenat Diagn. 2012. PMID: 22903415

10

Low uptake of the combined test in The Netherlands--which factors contribute?

Bakker M, Birnie E, Pajkrt E, Bilardo CM, Snijders RJ. Bakker M, et al. Among authors: pajkrt e. Prenat Diagn. 2012 Dec;32(13):1305-12. doi: 10.1002/pd.4001. Epub 2012 Nov 8. Prenat Diagn. 2012. PMID: 23138694

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