Vase P - Search Results

1

Hereditary haemorrhagic telangiectasia: a population-based study of prevalence and mortality in Danish patients.

Kjeldsen AD, Vase P, Green A. Kjeldsen AD, et al. Among authors: vase p. J Intern Med. 1999 Jan;245(1):31-9. doi: 10.1046/j.1365-2796.1999.00398.x. J Intern Med. 1999. PMID: 10095814 Free 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: vase p. Acta Radiol. 1998 Nov;39(6):723-6. doi: 10.3109/02841859809175505. Acta Radiol. 1998. PMID: 9817050

3

Pulmonary arteriovenous malformations: screening procedures and pulmonary angiography in patients with hereditary hemorrhagic telangiectasia.

Kjeldsen AD, Oxhøj H, Andersen PE, Elle B, Jacobsen JP, Vase P. Kjeldsen AD, et al. Among authors: vase p. Chest. 1999 Aug;116(2):432-9. doi: 10.1378/chest.116.2.432. Chest. 1999. PMID: 10453873

4

Prevalence of pulmonary arteriovenous malformations (PAVMs) and occurrence of neurological symptoms in patients with hereditary haemorrhagic telangiectasia (HHT).

Kjeldsen AD, Oxhøj H, Andersen PE, Green A, Vase P. Kjeldsen AD, et al. Among authors: vase p. J Intern Med. 2000 Sep;248(3):255-62. doi: 10.1046/j.1365-2796.2000.00725.x. J Intern Med. 2000. PMID: 10971793 Free article.

5

[Hereditary hemorrhagic telangiectasia. A population-based study on prevalence and mortality among Danish HHT patients].

Kjeldsen AD, Vase P, Green A. Kjeldsen AD, et al. Among authors: vase p. Ugeskr Laeger. 2000 Jun 19;162(25):3597-601. Ugeskr Laeger. 2000. PMID: 11016284 Danish.

6

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. Among authors: vase p. 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

7

Mutations in endoglin and in activin receptor-like kinase 1 among Danish patients with hereditary haemorrhagic telangiectasia.

Brusgaard K, Kjeldsen AD, Poulsen L, Moss H, Vase P, Rasmussen K, Kruse TA, Hørder M. Brusgaard K, et al. Among authors: vase p. Clin Genet. 2004 Dec;66(6):556-61. doi: 10.1111/j.1399-0004.2004.00341.x. Clin Genet. 2004. PMID: 15521985

8

Clinical symptoms according to genotype amongst patients with hereditary haemorrhagic telangiectasia.

Kjeldsen AD, Møller TR, Brusgaard K, Vase P, Andersen PE. Kjeldsen AD, et al. Among authors: vase p. J Intern Med. 2005 Oct;258(4):349-55. doi: 10.1111/j.1365-2796.2005.01555.x. J Intern Med. 2005. PMID: 16164574 Free article.

9

Group specific component in serum and otosclerosis: no association.

Kjeldsen AD, Vase P, Thymann M, Green A, Morling N. Kjeldsen AD, et al. Among authors: vase p. Acta Otolaryngol. 1994 May;114(3):303-4. doi: 10.3109/00016489409126060. Acta Otolaryngol. 1994. PMID: 8073863

10

Hereditary hemorrhagic telangiectasia.

Kjeldsen AD, Vase P, Oxhøj H. Kjeldsen AD, et al. Among authors: vase p. N Engl J Med. 1996 Feb 1;334(5):331-2. N Engl J Med. 1996. PMID: 8532039 No abstract available.

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