Paus B - Search Results

1

Ocular findings in 87 adults with Ghent-1 verified Marfan syndrome.

Drolsum L, Rand-Hendriksen S, Paus B, Geiran OR, Semb SO. Drolsum L, et al. Among authors: paus b. Acta Ophthalmol. 2015 Feb;93(1):46-53. doi: 10.1111/aos.12448. Epub 2014 May 22. Acta Ophthalmol. 2015. PMID: 24853997 Free article.

2

Search for correlations between FBN1 genotype and complete Ghent phenotype in 44 unrelated Norwegian patients with Marfan syndrome.

Rand-Hendriksen S, Tjeldhorn L, Lundby R, Semb SO, Offstad J, Andersen K, Geiran O, Paus B. Rand-Hendriksen S, et al. Among authors: paus b. Am J Med Genet A. 2007 Sep 1;143A(17):1968-77. doi: 10.1002/ajmg.a.31759. Am J Med Genet A. 2007. PMID: 17663468

3

Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome.

Rand-Hendriksen S, Lundby R, Tjeldhorn L, Andersen K, Offstad J, Semb SO, Smith HJ, Paus B, Geiran O. Rand-Hendriksen S, et al. Among authors: paus b. Eur J Hum Genet. 2009 Oct;17(10):1222-30. doi: 10.1038/ejhg.2009.30. Epub 2009 Mar 18. Eur J Hum Genet. 2009. PMID: 19293838 Free PMC article.

4

Survival, causes of death, and cardiovascular events in patients with Marfan syndrome.

Vanem TT, Geiran OR, Krohg-Sørensen K, Røe C, Paus B, Rand-Hendriksen S. Vanem TT, et al. Among authors: paus b. Mol Genet Genomic Med. 2018 Nov;6(6):1114-1123. doi: 10.1002/mgg3.489. Epub 2018 Nov 4. Mol Genet Genomic Med. 2018. PMID: 30393980 Free PMC article.

5

Marfan syndrome: Evolving organ manifestations-A 10-year follow-up study.

Vanem TT, Böker T, Sandvik GF, Kirkhus E, Smith HJ, Andersen K, Drolsum L, Lundby R, Røe C, Krohg-Sørensen K, Geiran OR, Paus B, Rand-Hendriksen S. Vanem TT, et al. Among authors: paus b. Am J Med Genet A. 2020 Feb;182(2):397-408. doi: 10.1002/ajmg.a.61441. Epub 2019 Dec 11. Am J Med Genet A. 2020. PMID: 31825148

6

Dural ectasia in Marfan syndrome: a case control study.

Lundby R, Rand-Hendriksen S, Hald JK, Lilleås FG, Pripp AH, Skaar S, Paus B, Geiran O, Smith HJ. Lundby R, et al. Among authors: paus b. AJNR Am J Neuroradiol. 2009 Sep;30(8):1534-40. doi: 10.3174/ajnr.A1620. Epub 2009 May 20. AJNR Am J Neuroradiol. 2009. PMID: 19461064 Free PMC article.

7

Qualitative and quantitative analysis of FBN1 mRNA from 16 patients with Marfan Syndrome.

Tjeldhorn L, Amundsen SS, Barøy T, Rand-Hendriksen S, Geiran O, Frengen E, Paus B. Tjeldhorn L, et al. Among authors: paus b. BMC Med Genet. 2015 Dec 18;16:113. doi: 10.1186/s12881-015-0260-4. BMC Med Genet. 2015. PMID: 26684006 Free PMC article.

8

Dural ectasia in Marfan syndrome and other hereditary connective tissue disorders: a 10-year follow-up study.

Böker T, Vanem TT, Pripp AH, Rand-Hendriksen S, Paus B, Smith HJ, Lundby R. Böker T, et al. Among authors: paus b. Spine J. 2019 Aug;19(8):1412-1421. doi: 10.1016/j.spinee.2019.04.010. Epub 2019 Apr 15. Spine J. 2019. PMID: 30998996 Free article.

9

Rapid and efficient FBN1 mutation detection using automated sample preparation and direct sequencing as the primary strategy.

Tjeldhorn L, Rand-Hendriksen S, Gervin K, Brandal K, Inderhaug E, Geiran O, Paus B. Tjeldhorn L, et al. Among authors: paus b. Genet Test. 2006 Winter;10(4):258-64. doi: 10.1089/gte.2006.258-264. Genet Test. 2006. PMID: 17253931

10

Cardiovascular surgery in Loeys-Dietz syndrome types 1-4.

Krohg-Sørensen K, Lingaas PS, Lundblad R, Seem E, Paus B, Geiran OR. Krohg-Sørensen K, et al. Among authors: paus b. Eur J Cardiothorac Surg. 2017 Dec 1;52(6):1125-1131. doi: 10.1093/ejcts/ezx147. Eur J Cardiothorac Surg. 2017. PMID: 28541520

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