Havndrup O - Search Results

1

Clinical and genetic characteristics of alpha cardiac actin gene mutations in hypertrophic cardiomyopathy.

Mogensen J, Perrot A, Andersen PS, Havndrup O, Klausen IC, Christiansen M, Bross P, Egeblad H, Bundgaard H, Osterziel KJ, Haltern G, Lapp H, Reinecke P, Gregersen N, Børglum AD. Mogensen J, et al. Among authors: havndrup o. J Med Genet. 2004 Jan;41(1):e10. doi: 10.1136/jmg.2003.010447. J Med Genet. 2004. PMID: 14729850 Free PMC article. No abstract available.

2

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: havndrup o. 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.

3

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.

Andersen PS, Havndrup O, Bundgaard H, Moolman-Smook JC, Larsen LA, Mogensen J, Brink PA, Børglum AD, Corfield VA, Kjeldsen K, Vuust J, Christiansen M. Andersen PS, et al. Among authors: havndrup o. J Med Genet. 2001 Dec;38(12):E43. doi: 10.1136/jmg.38.12.e43. J Med Genet. 2001. PMID: 11748309 Free PMC article. No abstract available.

4

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations.

Havndrup O, Bundgaard H, Andersen PS, Allan Larsen L, Vuust J, Kjeldsen K, Christiansen M. Havndrup O, et al. Cardiovasc Res. 2003 Feb;57(2):347-57. doi: 10.1016/s0008-6363(02)00711-3. Cardiovasc Res. 2003. PMID: 12566107

5

Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency.

Andersen PS, Havndrup O, Bundgaard H, Larsen LA, Vuust J, Pedersen AK, Kjeldsen K, Christiansen M. Andersen PS, et al. Among authors: havndrup o. Eur J Hum Genet. 2004 Aug;12(8):673-7. doi: 10.1038/sj.ejhg.5201190. Eur J Hum Genet. 2004. PMID: 15114369

6

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. Among authors: havndrup o. J Mol Cell Cardiol. 1999 Apr;31(4):745-50. doi: 10.1006/jmcc.1998.0911. J Mol Cell Cardiol. 1999. PMID: 10329202

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. Scand Cardiovasc J. 2000 Dec;34(6):558-63. doi: 10.1080/140174300750064477. Scand Cardiovasc J. 2000. PMID: 11214007 Free article.

8

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. 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.

9

One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region.

Hougs L, Havndrup O, Bundgaard H, Køber L, Vuust J, Larsen LA, Christiansen M, Andersen PS. Hougs L, et al. Among authors: havndrup o. Eur J Hum Genet. 2005 Feb;13(2):161-5. doi: 10.1038/sj.ejhg.5201310. Eur J Hum Genet. 2005. PMID: 15483641

10

[Hypertrophic cardiomyopathy].

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

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