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Adverse reactions to injectable soft tissue permanent fillers.
Christensen L, Breiting V, Janssen M, Vuust J, Hogdall E. Christensen L, et al. Among authors: vuust j. Aesthetic Plast Surg. 2005 Jan-Feb;29(1):34-48. doi: 10.1007/s00266-004-0113-6. Epub 2005 Mar 11. Aesthetic Plast Surg. 2005. PMID: 15759096 Review.
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.
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
Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles.
Larsen LA, Armstrong JS, Grønskov K, Hjalgrim H, Macpherson JN, Brøndum-Nielsen K, Hasholt L, Nørgaard-Pedersen B, Vuust J. Larsen LA, et al. Am J Med Genet. 2000 Jul 17;93(2):99-106. doi: 10.1002/1096-8628(20000717)93:2<99::aid-ajmg4>3.0.co;2-w. Am J Med Genet. 2000. PMID: 10869110
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. 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.
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. 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.
Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2.
Larsen LA, Svendsen IH, Jensen AM, Kanters JK, Andersen PS, Møller M, Sørensen SA, Sandøe E, Jacobsen JR, Vuust J, Christiansen M. Larsen LA, et al. Clin Genet. 2000 Feb;57(2):125-30. doi: 10.1034/j.1399-0004.2000.570206.x. Clin Genet. 2000. PMID: 10735633
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
An efficient cellular system for mutational analysis of prohormone processing.
Bundgaard JR, Cowland JB, Vuust J, Rehfeld JF. Bundgaard JR, et al. DNA Cell Biol. 1996 Feb;15(2):147-57. doi: 10.1089/dna.1996.15.147. DNA Cell Biol. 1996. PMID: 8634142
Evaluation of a polymorphism in intron 2 of the p53 gene in ovarian cancer patients. From the Danish "Malova" Ovarian Cancer Study.
Høgdall EV, Kjaer SK, Glud E, Christensen L, Blaakaer J, Vuust J, Bock JE, Norgaard-Pedersen B, Hogdall CK. Høgdall EV, et al. Among authors: vuust j. Anticancer Res. 2003 Jul-Aug;23(4):3397-404. Anticancer Res. 2003. PMID: 12926080
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