Bundgaard H - Search Results

1

Left ventricular volume predicts exercise capacity in hypertrophic cardiomyopathy.

Axelsson A, Iversen K, Vejlstrup N, Langhoff L, Thomsen A, Ho CY, Havndrup O, Kofoed KF, Jensen M, Bundgaard H. Axelsson A, et al. Among authors: bundgaard h. Int J Cardiol. 2016 Jan 15;203:676-8. doi: 10.1016/j.ijcard.2015.11.029. Epub 2015 Nov 6. Int J Cardiol. 2016. PMID: 26583841 No abstract available.

2

[Hypertrophic cardiomyopathy].

Bundgaard H, Havndrup O, Høst U, Kelbaek H. Bundgaard H, et al. Ugeskr Laeger. 1998 Sep 14;160(38):5478-83. Ugeskr Laeger. 1998. PMID: 9763919 Review. Danish.

3

[Treatment of hypertrophic cardiomyopathy].

Havndrup O, Bundgaard H, Hansen FV, Pietersen AH, Kelbaek HS. Havndrup O, et al. Among authors: bundgaard h. Ugeskr Laeger. 1998 Sep 14;160(38):5495-500. Ugeskr Laeger. 1998. PMID: 9763923 Danish.

4

Mutation Detection by Cleavase in Combination With Capillary Electrophoresis Analysis: Application to Mutations Causing Hypertrophic Cardiomyopathy and Long-QT Syndrome.

Andersen PS, Larsen LA, Kanters Jr Jr, Havndrup O, Bundgaard H, Brandt NJ, Vuust J, Christiansen M. Andersen PS, et al. Among authors: bundgaard h. Mol Diagn. 1998 Jun;3(2):105-111. doi: 10.154/MODI00300105. Mol Diagn. 1998. PMID: 10029661

5

Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain.

Bundgaard H, Havndrup O, Andersen PS, Larsen LA, Brandt NJ, Vuust J, Kjeldsen K, Christiansen M. Bundgaard H, et al. J Mol Cell Cardiol. 1999 Apr;31(4):745-50. doi: 10.1006/jmcc.1998.0911. J Mol Cell Cardiol. 1999. PMID: 10329202

6

Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene.

Andersen PS, Havndrup O, Bundgaard H, Larsen LA, Vuust J, Kjeldsen K, Christiansen M. Andersen PS, et al. Among authors: bundgaard h. Clin Genet. 1999 Sep;56(3):244-6. doi: 10.1034/j.1399-0004.1999.560313.x. Clin Genet. 1999. PMID: 10563488 No abstract available.

7

A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy.

Havndrup O, Bundgaard H, Andersen PS, Larsen LA, Vuust J, Kjeldsen K, Christiansen M. Havndrup O, et al. Among authors: bundgaard h. Scand Cardiovasc J. 2000 Dec;34(6):558-63. doi: 10.1080/140174300750064477. Scand Cardiovasc J. 2000. PMID: 11214007 Free article.

8

Outcome of septal myectomy in patients with hypertrophic obstructive cardiomyopathy.

Havndrup O, Pettersson G, Kjeldsen K, Bundgaard H. Havndrup O, et al. Among authors: bundgaard h. Scand Cardiovasc J. 2000 Dec;34(6):564-9. doi: 10.1080/140174300750064486. Scand Cardiovasc J. 2000. PMID: 11214008 Free article.

9

The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.

Havndrup O, Bundgaard H, Andersen PS, Larsen LA, Vuust J, Kjeldsen K, Christiansen M. Havndrup O, et al. Among authors: bundgaard h. Am J Cardiol. 2001 Jun 1;87(11):1315-7. doi: 10.1016/s0002-9149(01)01532-6. Am J Cardiol. 2001. PMID: 11377367 No abstract available.

10

Predictors of coronary in-stent restenosis: importance of angiotensin-converting enzyme gene polymorphism and treatment with angiotensin-converting enzyme inhibitors.

Jørgensen E, Kelbaek H, Helqvist S, Jensen GV, Saunamäki K, Kastrup J, Havndrup O, Bundgaard H, Kyst Madsen J, Christiansen M, Andersen PS, Reiber JH. Jørgensen E, et al. Among authors: bundgaard h. J Am Coll Cardiol. 2001 Nov 1;38(5):1434-9. doi: 10.1016/s0735-1097(01)01580-7. J Am Coll Cardiol. 2001. PMID: 11691520 Free article.

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