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
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2002 | 1 |
2004 | 1 |
2008 | 3 |
2010 | 1 |
2011 | 1 |
2024 | 0 |
PubMed (cited) for id: 615396
7 results
Results by year
Filters applied: . Clear all
Page 1
Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
Circ Cardiovasc Genet. 2011 Aug 1;4(4):367-74. doi: 10.1161/CIRCGENETICS.110.959270. Epub 2011 May 6.
Circ Cardiovasc Genet. 2011.
PMID: 21551322
Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy.
Hershberger RE, Norton N, Morales A, Li D, Siegfried JD, Gonzalez-Quintana J.
Hershberger RE, et al.
Circ Cardiovasc Genet. 2010 Apr;3(2):155-61. doi: 10.1161/CIRCGENETICS.109.912345. Epub 2010 Mar 9.
Circ Cardiovasc Genet. 2010.
PMID: 20215591
Free PMC article.
Item in Clipboard
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
Hershberger RE, Parks SB, Kushner JD, Li D, Ludwigsen S, Jakobs P, Nauman D, Burgess D, Partain J, Litt M.
Hershberger RE, et al.
Clin Transl Sci. 2008 May;1(1):21-6. doi: 10.1111/j.1752-8062.2008.00017.x.
Clin Transl Sci. 2008.
PMID: 19412328
Free PMC article.
Item in Clipboard
Adverse events in families with hypertrophic or dilated cardiomyopathy and mutations in the MYBPC3 gene.
Ehlermann P, Weichenhan D, Zehelein J, Steen H, Pribe R, Zeller R, Lehrke S, Zugck C, Ivandic BT, Katus HA.
Ehlermann P, et al.
BMC Med Genet. 2008 Oct 28;9:95. doi: 10.1186/1471-2350-9-95.
BMC Med Genet. 2008.
PMID: 18957093
Free PMC article.
Item in Clipboard
Shared genetic causes of cardiac hypertrophy in children and adults.
Morita H, Rehm HL, Menesses A, McDonough B, Roberts AE, Kucherlapati R, Towbin JA, Seidman JG, Seidman CE.
Morita H, et al.
N Engl J Med. 2008 May 1;358(18):1899-908. doi: 10.1056/NEJMoa075463. Epub 2008 Apr 9.
N Engl J Med. 2008.
PMID: 18403758
Free PMC article.
Item in Clipboard
Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy.
Van Driest SL, Vasile VC, Ommen SR, Will ML, Tajik AJ, Gersh BJ, Ackerman MJ.
Van Driest SL, et al.
J Am Coll Cardiol. 2004 Nov 2;44(9):1903-10. doi: 10.1016/j.jacc.2004.07.045.
J Am Coll Cardiol. 2004.
PMID: 15519027
Free article.
Item in Clipboard
Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.
Daehmlow S, Erdmann J, Knueppel T, Gille C, Froemmel C, Hummel M, Hetzer R, Regitz-Zagrosek V.
Daehmlow S, et al.
Biochem Biophys Res Commun. 2002 Oct 18;298(1):116-20. doi: 10.1016/s0006-291x(02)02374-4.
Biochem Biophys Res Commun. 2002.
PMID: 12379228
Item in Clipboard
Cite
Cite