Vestergaard EM - Search Results

1

Aggressive medullary thyroid carcinoma in a ten-year-old patient with multiple endocrine neoplasia 2B due to the A883F mutation.

Mathiesen JS, Stochholm K, Poulsen PL, Vestergaard EM, Christiansen P, Vestergaard P. Mathiesen JS, et al. Among authors: vestergaard em, vestergaard p. Thyroid. 2015 Jan;25(1):139-40. doi: 10.1089/thy.2014.0177. Thyroid. 2015. PMID: 25244518 No abstract available.

2

Codon Y791F mutations in a large kindred: is prophylactic thyroidectomy always indicated?

Vestergaard P, Vestergaard EM, Brockstedt H, Christiansen P. Vestergaard P, et al. Among authors: vestergaard em. World J Surg. 2007 May;31(5):996-1001; discussion 1002-4. doi: 10.1007/s00268-006-0446-1. World J Surg. 2007. PMID: 17483988

3

Ocular albinism with infertility and late-onset sensorineural hearing loss.

Fabian-Jessing BK, Vestergaard EM, Plomp AS, Bergen AA, Dreschler WA, Duno M, Winiarska BS, Neumann L, Gaihede M, Vorum H, Petersen MB. Fabian-Jessing BK, et al. Among authors: vestergaard em. Am J Med Genet A. 2018 Jul;176(7):1587-1593. doi: 10.1002/ajmg.a.38836. Am J Med Genet A. 2018. PMID: 30160833

4

17q12 deletion and duplication syndrome in Denmark-A clinical cohort of 38 patients and review of the literature.

Rasmussen M, Vestergaard EM, Graakjaer J, Petkov Y, Bache I, Fagerberg C, Kibaek M, Svaneby D, Petersen OB, Brasch-Andersen C, Sunde L. Rasmussen M, et al. Among authors: vestergaard em. Am J Med Genet A. 2016 Nov;170(11):2934-2942. doi: 10.1002/ajmg.a.37848. Epub 2016 Jul 13. Am J Med Genet A. 2016. PMID: 27409573 Review.

5

Clinical presentations of 23 half-siblings from a mosaic neurofibromatosis type 1 sperm donor.

Ejerskov C, Farholt S, Skovby F, Vestergaard EM, Haagerup A. Ejerskov C, et al. Among authors: vestergaard em. Clin Genet. 2016 Mar;89(3):346-50. doi: 10.1111/cge.12600. Epub 2015 May 15. Clin Genet. 2016. PMID: 25872886

6

Prenatal diagnosis of Nager syndrome in a 12-week-old fetus with a whole gene deletion of SF3B4 by chromosomal microarray.

Lund IC, Vestergaard EM, Christensen R, Uldbjerg N, Becher N. Lund IC, et al. Among authors: vestergaard em. Eur J Med Genet. 2016 Jan;59(1):48-51. doi: 10.1016/j.ejmg.2015.12.001. Epub 2015 Dec 9. Eur J Med Genet. 2016. PMID: 26679067

7

Placental mosaicism in the era of chromosomal microarrays.

Vogel I, Vestergaard EM, Lildballe DL, Christensen R, Hoseth GE, Petersen AC, Bogaard P, Sørensen AN. Vogel I, et al. Among authors: vestergaard em. Eur J Med Genet. 2020 Apr;63(4):103778. doi: 10.1016/j.ejmg.2019.103778. Epub 2019 Sep 30. Eur J Med Genet. 2020. PMID: 31580923

8

First reported case of Simpson-Golabi-Behmel syndrome in a female fetus diagnosed prenatally with chromosomal microarray.

Støve HK, Becher N, Gjørup V, Ramsing M, Vogel I, Vestergaard EM. Støve HK, et al. Among authors: vestergaard em. Clin Case Rep. 2017 Mar 17;5(5):608-612. doi: 10.1002/ccr3.902. eCollection 2017 May. Clin Case Rep. 2017. PMID: 28469860 Free PMC article.

9

Trefoil factors in inflammatory bowel disease.

Aamann L, Vestergaard EM, Grønbæk H. Aamann L, et al. Among authors: vestergaard em. World J Gastroenterol. 2014 Mar 28;20(12):3223-30. doi: 10.3748/wjg.v20.i12.3223. World J Gastroenterol. 2014. PMID: 24696606 Free PMC article. Review.

10

High-resolution melting analysis using unlabeled probe and amplicon scanning simultaneously detects several lactase persistence variants.

Janukonyté J, Vestergaard EM, Ladefoged SA, Nissen PH. Janukonyté J, et al. Among authors: vestergaard em. Scand J Clin Lab Invest. 2010 Dec;70(8):535-40. doi: 10.3109/00365513.2010.522251. Epub 2010 Oct 28. Scand J Clin Lab Invest. 2010. PMID: 21028949

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

52 results

Search Page

Filters