Kanters J - Search Results

1

[Short QT syndrome as an inherited condition].

Møller DV, Hedley PL, Olesen M, Kanters J, Svendsen JH, Christiansen M. Møller DV, et al. Among authors: kanters j. Ugeskr Laeger. 2011 Feb 7;173(6):420-4. Ugeskr Laeger. 2011. PMID: 21299935 Review. Danish.

2

Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome.

Kanters JK, Larsen LA, Orholm M, Agner E, Andersen PS, Vuust J, Christiansen M. Kanters JK, et al. J Cardiovasc Electrophysiol. 1998 Jun;9(6):620-4. doi: 10.1111/j.1540-8167.1998.tb00944.x. J Cardiovasc Electrophysiol. 1998. PMID: 9654228

3

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome.

Larsen LA, Andersen PS, Kanters JK, Jacobsen JR, Vuust J, Christiansen M. Larsen LA, et al. Among authors: kanters jk. Clin Chim Acta. 1999 Feb;280(1-2):113-25. doi: 10.1016/s0009-8981(98)00177-6. Clin Chim Acta. 1999. PMID: 10090529

4

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

Larsen LA, Fosdal I, Andersen PS, Kanters JK, Vuust J, Wettrell G, Christiansen M. Larsen LA, et al. Among authors: kanters jk. Eur J Hum Genet. 1999 Sep;7(6):724-8. doi: 10.1038/sj.ejhg.5200323. Eur J Hum Genet. 1999. PMID: 10482963

5

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. Among authors: kanters jk. Clin Genet. 2000 Feb;57(2):125-30. doi: 10.1034/j.1399-0004.2000.570206.x. Clin Genet. 2000. PMID: 10735633

6

[Molecular genetics of the long QT syndrome. Genes causing syncope and sudden death].

Fosdal I, Wettrell G, Christiansen M, Kanters JK, Larsen LA. Fosdal I, et al. Among authors: kanters jk. Lakartidningen. 2001 Feb 21;98(8):810-5. Lakartidningen. 2001. PMID: 11265565 Review. Swedish.

7

Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.

Larsen LA, Andersen PS, Kanters J, Svendsen IH, Jacobsen JR, Vuust J, Wettrell G, Tranebjaerg L, Bathen J, Christiansen M. Larsen LA, et al. Among authors: kanters j. Clin Chem. 2001 Aug;47(8):1390-5. Clin Chem. 2001. PMID: 11468227

8

Long QT syndrome patients may faint due to neurocardiogenic syncope.

Toft E, Aarøe J, Jensen BT, Christiansen M, Fog L, Thomsen PE, Kanters JK. Toft E, et al. Among authors: kanters jk. Europace. 2003 Oct;5(4):367-70. doi: 10.1016/s1099-5129(03)00083-7. Europace. 2003. PMID: 14753633

9

Does KCNE5 play a role in long QT syndrome?

Hofman-Bang J, Jespersen T, Grunnet M, Larsen LA, Andersen PS, Kanters JK, Kjeldsen K, Christiansen M. Hofman-Bang J, et al. Among authors: kanters jk. Clin Chim Acta. 2004 Jul;345(1-2):49-53. doi: 10.1016/j.cccn.2004.02.033. Clin Chim Acta. 2004. PMID: 15193977

10

Mutations in the HERG K+-ion channel: a novel link between long QT syndrome and sudden infant death syndrome.

Christiansen M, Tønder N, Larsen LA, Andersen PS, Simonsen H, Oyen N, Kanters JK, Jacobsen JR, Fosdal I, Wettrell G, Kjeldsen K. Christiansen M, et al. Am J Cardiol. 2005 Feb 1;95(3):433-4. doi: 10.1016/j.amjcard.2004.09.054. Am J Cardiol. 2005. PMID: 15670565

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