Fellmann F - Search Results

1

Patient with syncope and LQTS carrying a mutation in the PAS domain of the hERG1 channel.

Grilo LS, Schläpfer J, Fellmann F, Abriel H. Grilo LS, et al. Among authors: fellmann f. Ann Noninvasive Electrocardiol. 2011 Apr;16(2):213-8. doi: 10.1111/j.1542-474X.2011.00419.x. Ann Noninvasive Electrocardiol. 2011. PMID: 21496174 Free PMC article.

2

Takotsubo cardiomyopathy and congenital long QT syndrome in a patient with a novel duplication in the Per-Arnt-Sim (PAS) domain of hERG1.

Grilo LS, Pruvot E, Grobéty M, Castella V, Fellmann F, Abriel H. Grilo LS, et al. Among authors: fellmann f. Heart Rhythm. 2010;7(2):260-5. doi: 10.1016/j.hrthm.2009.09.026. Epub 2009 Sep 24. Heart Rhythm. 2010. PMID: 20004623 No abstract available.

3

Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration.

Michaud K, Fellmann F, Abriel H, Beckmann JS, Mangin P, Elger BS. Michaud K, et al. Among authors: fellmann f. Swiss Med Wkly. 2009 Dec 12;139(49-50):712-8. doi: 10.4414/smw.2009.12837. Swiss Med Wkly. 2009. PMID: 20047134 Free article. Review.

4

Sudden cardiac death in the young (5-39 years) in the canton of Vaud, Switzerland.

Hofer F, Fellmann F, Schläpfer J, Michaud K. Hofer F, et al. Among authors: fellmann f. BMC Cardiovasc Disord. 2014 Oct 7;14:140. doi: 10.1186/1471-2261-14-140. BMC Cardiovasc Disord. 2014. PMID: 25291980 Free PMC article.

5

[Multidisciplinary cardiogenetic counselling].

Fellmann F, Jeanrenaud X, Sekarski N, Michaud K, Hersch D, Fodstad H, Bhuiyan ZA, Schläpfer J. Fellmann F, et al. Rev Med Suisse. 2017 May 24;13(564):1094-1099. Rev Med Suisse. 2017. PMID: 28639772 French.

6

ACTN2 variant associated with a cardiac phenotype suggestive of left-dominant arrhythmogenic cardiomyopathy.

Good JM, Fellmann F, Bhuiyan ZA, Rotman S, Pruvot E, Schläpfer J. Good JM, et al. Among authors: fellmann f. HeartRhythm Case Rep. 2019 Oct 7;6(1):15-19. doi: 10.1016/j.hrcr.2019.10.001. eCollection 2020 Jan. HeartRhythm Case Rep. 2019. PMID: 31956495 Free PMC article. No abstract available.

7

Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes.

Pipilas DC, Johnson CN, Webster G, Schlaepfer J, Fellmann F, Sekarski N, Wren LM, Ogorodnik KV, Chazin DM, Chazin WJ, Crotti L, Bhuiyan ZA, George AL Jr. Pipilas DC, et al. Among authors: fellmann f. Heart Rhythm. 2016 Oct;13(10):2012-9. doi: 10.1016/j.hrthm.2016.06.038. Epub 2016 Jul 1. Heart Rhythm. 2016. PMID: 27374306 Free PMC article.

8

Confirmation of the origin of NISCH syndrome.

Feldmeyer L, Huber M, Fellmann F, Beckmann JS, Frenk E, Hohl D. Feldmeyer L, et al. Among authors: fellmann f. Hum Mutat. 2006 May;27(5):408-10. doi: 10.1002/humu.20333. Hum Mutat. 2006. PMID: 16619213

9

[Molecular autopsy of sudden cardiac death: from postmortem to clinical approach].

Michaud K, Lesta Mdel M, Fellmann F, Mangin P. Michaud K, et al. Among authors: fellmann f. Rev Med Suisse. 2008 Jul 2;4(164):1590-3. Rev Med Suisse. 2008. PMID: 18711970 French.

10

Sudden death: ethical and legal problems of post-mortem forensic genetic testing for hereditary cardiac diseases.

Elger BS, Michaud K, Fellmann F, Mangin P. Elger BS, et al. Among authors: fellmann f. Clin Genet. 2010 Mar;77(3):287-92. doi: 10.1111/j.1399-0004.2009.01293.x. Epub 2009 Oct 23. Clin Genet. 2010. PMID: 19863545

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

89 results

Search Page

Filters