Kjeldsen A - Search Results

1

Safety of direct oral anticoagulants in patients with hereditary hemorrhagic telangiectasia.

Shovlin CL, Millar CM, Droege F, Kjeldsen A, Manfredi G, Suppressa P, Ugolini S, Coote N, Fialla AD, Geisthoff U, Lenato GM, Mager HJ, Pagella F, Post MC, Sabbà C, Sure U, Torring PM, Dupuis-Girod S, Buscarini E; VASCERN-HHT. Shovlin CL, et al. Among authors: kjeldsen a. Orphanet J Rare Dis. 2019 Aug 28;14(1):210. doi: 10.1186/s13023-019-1179-1. Orphanet J Rare Dis. 2019. PMID: 31462308 Free PMC article.

2

Embolotherapy for pulmonary arteriovenous malformations in patients with hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).

Andersen PE, Kjeldsen AD, Oxhøj H, Vase P, White RI Jr. Andersen PE, et al. Among authors: kjeldsen ad. Acta Radiol. 1998 Nov;39(6):723-6. doi: 10.3109/02841859809175505. Acta Radiol. 1998. PMID: 9817050

3

Gastrointestinal bleeding in patients with hereditary hemorrhagic telangiectasia.

Kjeldsen AD, Kjeldsen J. Kjeldsen AD, et al. Among authors: kjeldsen j. Am J Gastroenterol. 2000 Feb;95(2):415-8. doi: 10.1111/j.1572-0241.2000.01792.x. Am J Gastroenterol. 2000. PMID: 10685743

4

Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).

Shovlin CL, Guttmacher AE, Buscarini E, Faughnan ME, Hyland RH, Westermann CJ, Kjeldsen AD, Plauchu H. Shovlin CL, et al. Among authors: kjeldsen ad. Am J Med Genet. 2000 Mar 6;91(1):66-7. doi: 10.1002/(sici)1096-8628(20000306)91:1<66::aid-ajmg12>3.0.co;2-p. Am J Med Genet. 2000. PMID: 10751092

5

Mutations in the ALK-1 gene and the phenotype of hereditary hemorrhagic telangiectasia in two large Danish families.

Kjeldsen AD, Brusgaard K, Poulsen L, Kruse T, Rasmussen K, Green A, Vase P. Kjeldsen AD, et al. Am J Med Genet. 2001 Feb 1;98(4):298-302. doi: 10.1002/1096-8628(20010201)98:4<298::aid-ajmg1093>3.0.co;2-k. Am J Med Genet. 2001. PMID: 11170071

6

[Diagnosis and treatment of morbus Osler].

Kjeldsen AD, Andersen PE, Tørring PM. Kjeldsen AD, et al. Ugeskr Laeger. 2011 Feb 14;173(7):490-5. Ugeskr Laeger. 2011. PMID: 21320413 Review. Danish.

7

Allelic dropout in the ENG gene, affecting the results of genetic testing in hereditary hemorrhagic telangiectasia.

Tørring PM, Kjeldsen AD, Ousager LB, Brasch-Andersen C, Brusgaard K. Tørring PM, et al. Genet Test Mol Biomarkers. 2012 Dec;16(12):1419-23. doi: 10.1089/gtmb.2012.0230. Epub 2012 Oct 9. Genet Test Mol Biomarkers. 2012. PMID: 23046070

8

Cerebral abscesses among Danish patients with hereditary haemorrhagic telangiectasia.

Kjeldsen AD, Tørring PM, Nissen H, Andersen PE. Kjeldsen AD, et al. Acta Neurol Scand. 2014 Mar;129(3):192-7. doi: 10.1111/ane.12167. Epub 2013 Aug 20. Acta Neurol Scand. 2014. PMID: 23962120

9

National mutation study among Danish patients with hereditary haemorrhagic telangiectasia.

Tørring PM, Brusgaard K, Ousager LB, Andersen PE, Kjeldsen AD. Tørring PM, et al. Among authors: kjeldsen ad. Clin Genet. 2014 Aug;86(2):123-33. doi: 10.1111/cge.12269. Epub 2013 Oct 3. Clin Genet. 2014. PMID: 24001356

10

Long non-coding RNA expression profiles in hereditary haemorrhagic telangiectasia.

Tørring PM, Larsen MJ, Kjeldsen AD, Ousager LB, Tan Q, Brusgaard K. Tørring PM, et al. PLoS One. 2014 Mar 6;9(3):e90272. doi: 10.1371/journal.pone.0090272. eCollection 2014. PLoS One. 2014. PMID: 24603890 Free PMC article.

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