Ulmer HE - Search Results

1

Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndrome.

Zehelein J, Thomas D, Khalil M, Wimmer AB, Koenen M, Licka M, Wu K, Kiehn J, Brockmeier K, Kreye VA, Karle CA, Katus HA, Ulmer HE, Schoels W. Zehelein J, et al. Among authors: ulmer he. Biochim Biophys Acta. 2004 Nov 5;1690(3):185-92. doi: 10.1016/j.bbadis.2004.06.024. Biochim Biophys Acta. 2004. PMID: 15511625 Free article.

2

Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.

Thomas D, Wimmer AB, Karle CA, Licka M, Alter M, Khalil M, Ulmer HE, Kathöfer S, Kiehn J, Katus HA, Schoels W, Koenen M, Zehelein J. Thomas D, et al. Among authors: ulmer he. Cardiovasc Res. 2005 Aug 15;67(3):487-97. doi: 10.1016/j.cardiores.2005.05.003. Cardiovasc Res. 2005. PMID: 15950200

3

Skipping of Exon 1 in the KCNQ1 gene causes Jervell and Lange-Nielsen syndrome.

Zehelein J, Kathoefer S, Khalil M, Alter M, Thomas D, Brockmeier K, Ulmer HE, Katus HA, Koenen M. Zehelein J, et al. Among authors: ulmer he. J Biol Chem. 2006 Nov 17;281(46):35397-403. doi: 10.1074/jbc.M603433200. Epub 2006 Sep 19. J Biol Chem. 2006. PMID: 16987820 Free article.

4

Biophysical characterization of KCNQ1 P320 mutations linked to long QT syndrome 1.

Thomas D, Khalil M, Alter M, Schweizer PA, Karle CA, Wimmer AB, Licka M, Katus HA, Koenen M, Ulmer HE, Zehelein J. Thomas D, et al. Among authors: ulmer he. J Mol Cell Cardiol. 2010 Jan;48(1):230-7. doi: 10.1016/j.yjmcc.2009.06.009. Epub 2009 Jun 21. J Mol Cell Cardiol. 2010. PMID: 19540844

5

[Inborn long QT-syndrome in childhood: clinical presentation and treatment].

Ulmer HE, Khalil M, Fischer M, Brockmeier K. Ulmer HE, et al. Herzschrittmacherther Elektrophysiol. 2002 Sep;13(3):130-41. doi: 10.1007/s00399-002-0349-2. Herzschrittmacherther Elektrophysiol. 2002. PMID: 24535447 German.

6

Identification and genotype related classification of children with long QT-syndrome using 24 h Holter recordings.

Bauch M, Siegler A, Khalil M, Zehelein J, Ulmer HE, Dickhaus H. Bauch M, et al. Among authors: ulmer he. Stud Health Technol Inform. 2007;129(Pt 2):1299-303. Stud Health Technol Inform. 2007. PMID: 17911924

7

Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation.

Luedde M, Ehlermann P, Weichenhan D, Will R, Zeller R, Rupp S, Müller A, Steen H, Ivandic BT, Ulmer HE, Kern M, Katus HA, Frey N. Luedde M, et al. Among authors: ulmer he. Cardiovasc Res. 2010 Jun 1;86(3):452-60. doi: 10.1093/cvr/cvq009. Epub 2010 Jan 18. Cardiovasc Res. 2010. PMID: 20083571

8

Prediction of normal QT intervals in children.

Eberle T, Hessling G, Ulmer HE, Brockmeier K. Eberle T, et al. Among authors: ulmer he. J Electrocardiol. 1998;31 Suppl:121-5. doi: 10.1016/s0022-0736(98)90303-x. J Electrocardiol. 1998. PMID: 9988015

9

Termination of atrial reentrant tachycardias by using transesophageal atrial pacing.

Brockmeier K, Ulmer HE, Hessling G. Brockmeier K, et al. Among authors: ulmer he. J Electrocardiol. 2002;35 Suppl:159-63. doi: 10.1054/jelc.2002.37174. J Electrocardiol. 2002. PMID: 12539114

10

Successful closure of the arterial duct in the setting of rubella syndrome.

Gorenflo M, Ulmer HE, Brockmeier K. Gorenflo M, et al. Among authors: ulmer he. Cardiol Young. 2002 Mar;12(2):200-2. doi: 10.1017/s1047951102000434. Cardiol Young. 2002. PMID: 12018732

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

97 results

Search Page

Filters