Bathen J - Search Results

1

High prevalence of exercise-induced arrhythmias in catecholaminergic polymorphic ventricular tachycardia mutation-positive family members diagnosed by cascade genetic screening.

Haugaa KH, Leren IS, Berge KE, Bathen J, Loennechen JP, Anfinsen OG, Früh A, Edvardsen T, Kongsgård E, Leren TP, Amlie JP. Haugaa KH, et al. Among authors: bathen j. Europace. 2010 Mar;12(3):417-23. doi: 10.1093/europace/eup448. Epub 2010 Jan 26. Europace. 2010. PMID: 20106799

2

The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome.

Schwartz PJ, Spazzolini C, Crotti L, Bathen J, Amlie JP, Timothy K, Shkolnikova M, Berul CI, Bitner-Glindzicz M, Toivonen L, Horie M, Schulze-Bahr E, Denjoy I. Schwartz PJ, et al. Among authors: bathen j. Circulation. 2006 Feb 14;113(6):783-90. doi: 10.1161/CIRCULATIONAHA.105.592899. Epub 2006 Feb 6. Circulation. 2006. PMID: 16461811

3

Jervell and Lange-Nielsen syndrome: a Norwegian perspective.

Tranebjaerg L, Bathen J, Tyson J, Bitner-Glindzicz M. Tranebjaerg L, et al. Among authors: bathen j. Am J Med Genet. 1999 Sep 24;89(3):137-46. Am J Med Genet. 1999. PMID: 10704188 Review.

4

Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen.

Tyson J, Tranebjaerg L, McEntagart M, Larsen LA, Christiansen M, Whiteford ML, Bathen J, Aslaksen B, Sørland SJ, Lund O, Pembrey ME, Malcolm S, Bitner-Glindzicz M. Tyson J, et al. Among authors: bathen j. Hum Genet. 2000 Nov;107(5):499-503. doi: 10.1007/s004390000402. Hum Genet. 2000. PMID: 11140949

5

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.

Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sørland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M. Tyson J, et al. Among authors: bathen j. Hum Mol Genet. 1997 Nov;6(12):2179-85. doi: 10.1093/hmg/6.12.2179. Hum Mol Genet. 1997. PMID: 9328483

6

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: bathen j. Clin Chem. 2001 Aug;47(8):1390-5. Clin Chem. 2001. PMID: 11468227

7

Impact of changes in heart rate and stroke volume on the cross sectional flow velocity distribution of diastolic mitral blood flow. A study on 6 patients with pacemakers programmed at different heart rates.

Samstad SO, Bathen J, Rossvoll O, Torp HG, Skjaerpe T, Hatle L. Samstad SO, et al. Among authors: bathen j. Int J Card Imaging. 1992;8(2):75-83. doi: 10.1007/BF01137528. Int J Card Imaging. 1992. PMID: 1629642

8

MR imaging of apical hypertrophic cardiomyopathy with left ventricular endomyocardial calcification.

Kvaerness J, Rinck PA, Bolz KD, Bathen J, Skjaerpe T. Kvaerness J, et al. Among authors: bathen j. J Comput Assist Tomogr. 1991 May-Jun;15(3):489-91. doi: 10.1097/00004728-199105000-00028. J Comput Assist Tomogr. 1991. PMID: 2026817

9

Massive left ventricular endomyocardial calcification associated with apical hypertrophic cardiomyopathy.

Bolz KD, Bathen J, Skjaerpe T, Halvorsen TB. Bolz KD, et al. Among authors: bathen j. Rofo. 1988 Oct;149(4):436-7. doi: 10.1055/s-2008-1048378. Rofo. 1988. PMID: 2845519 No abstract available.

10

Sinoatrial disease in acute myocardial infarction. Long-term prognosis.

Hatle L, Bathen J, Rokseth R. Hatle L, et al. Among authors: bathen j. Br Heart J. 1976 Apr;38(4):410-4. doi: 10.1136/hrt.38.4.410. Br Heart J. 1976. PMID: 1267985 Free PMC article.

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