Brusgaard K - Search Results

1

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: brusgaard k. 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

2

Insulinoma in childhood: a retrospective review of 22 patients from one referral centre.

Melikyan M, Gubaeva D, Shadrina A, Bolmasova A, Kareva M, Tiulpakov A, Efremenkov A, Sokolov Y, Brusgaard K, Christesen HT, Andersen K, Stepanov A, Averyanova J, Makarov S, Gurevich L. Melikyan M, et al. Among authors: brusgaard k. Front Endocrinol (Lausanne). 2023 Apr 19;14:1127173. doi: 10.3389/fendo.2023.1127173. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37152923 Free PMC article.

3

Three polymorphic mink, Mustela vison, dinucleotide repeats.

Brusgaard K, Shukri N, Malchenko SN, Lohi O, Christensen K, Kruse T. Brusgaard K, et al. Anim Genet. 1998 Apr;29(2):153. Anim Genet. 1998. PMID: 9699284 No abstract available.

4

A polymorphic mink (Mustela vison) dinucleotide repeat.

Brusgaard K, Malchenko SN, Christensen K, Lohi O, Kruse T. Brusgaard K, et al. Anim Genet. 1998 Dec;29(6):467. Anim Genet. 1998. PMID: 9883521 No abstract available.

5

Correspondence analysis of microarray time-course data in case-control design.

Tan Q, Brusgaard K, Kruse TA, Oakeley E, Hemmings B, Beck-Nielsen H, Hansen L, Gaster M. Tan Q, et al. Among authors: brusgaard k. J Biomed Inform. 2004 Oct;37(5):358-65. doi: 10.1016/j.jbi.2004.06.001. J Biomed Inform. 2004. PMID: 15488749 Free article.

6

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. Clin Genet. 2004 Dec;66(6):556-61. doi: 10.1111/j.1399-0004.2004.00341.x. Clin Genet. 2004. PMID: 15521985

7

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: brusgaard k. 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.

8

Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia.

Brusgaard K, Jordan P, Hansen H, Hansen AB, Hørder M. Brusgaard K, et al. Clin Genet. 2006 Mar;69(3):277-83. doi: 10.1111/j.1399-0004.2006.00585.x. Clin Genet. 2006. PMID: 16542394

9

Spotting and validation of a genome wide oligonucleotide chip with duplicate measurement of each gene.

Thomassen M, Skov V, Eiriksdottir F, Tan Q, Jochumsen K, Fritzner N, Brusgaard K, Dahlgaard J, Kruse TA. Thomassen M, et al. Among authors: brusgaard k. Biochem Biophys Res Commun. 2006 Jun 16;344(4):1111-20. doi: 10.1016/j.bbrc.2006.03.227. Epub 2006 Apr 19. Biochem Biophys Res Commun. 2006. PMID: 16647037

10

Reduced expression of nuclear-encoded genes involved in mitochondrial oxidative metabolism in skeletal muscle of insulin-resistant women with polycystic ovary syndrome.

Skov V, Glintborg D, Knudsen S, Jensen T, Kruse TA, Tan Q, Brusgaard K, Beck-Nielsen H, Højlund K. Skov V, et al. Among authors: brusgaard k. Diabetes. 2007 Sep;56(9):2349-55. doi: 10.2337/db07-0275. Epub 2007 Jun 11. Diabetes. 2007. PMID: 17563058 Free article.

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