Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 129

1.

Uptake of Predictive Genetic Testing and Cardiac Evaluation for Children at Risk for an Inherited Arrhythmia or Cardiomyopathy.

Christian S, Atallah J, Clegg R, Giuffre M, Huculak C, Dzwiniel T, Parboosingh J, Taylor S, Somerville M.

J Genet Couns. 2018 Feb;27(1):124-130. doi: 10.1007/s10897-017-0129-0. Epub 2017 Jul 11.

PMID:
28699125
2.

Family and population strategies for screening and counselling of inherited cardiac arrhythmias.

van Langen IM, Hofman N, Tan HL, Wilde AA.

Ann Med. 2004;36 Suppl 1:116-24.

PMID:
15176433
3.

Yield of molecular and clinical testing for arrhythmia syndromes: report of 15 years' experience.

Hofman N, Tan HL, Alders M, Kolder I, de Haij S, Mannens MM, Lombardi MP, Dit Deprez RH, van Langen I, Wilde AA.

Circulation. 2013 Oct 1;128(14):1513-21. doi: 10.1161/CIRCULATIONAHA.112.000091. Epub 2013 Aug 20.

PMID:
23963746
4.

Clinical and Genetic Diagnosis of Nonischemic Sudden Cardiac Death.

Jiménez-Jáimez J, Alcalde Martínez V, Jiménez Fernández M, Bermúdez Jiménez F, Rodríguez Vázquez Del Rey MDM, Perin F, Oyonarte Ramírez JM, López Fernández S, de la Torre I, García Orta R, González Molina M, Cabrerizo EM, Álvarez Abril B, Álvarez M, Macías Ruiz R, Correa C, Tercedor L.

Rev Esp Cardiol (Engl Ed). 2017 Oct;70(10):808-816. doi: 10.1016/j.rec.2017.04.024. Epub 2017 May 26. English, Spanish.

PMID:
28566242
5.

Familial cardiological and targeted genetic evaluation: low yield in sudden unexplained death and high yield in unexplained cardiac arrest syndromes.

Kumar S, Peters S, Thompson T, Morgan N, Maccicoca I, Trainer A, Zentner D, Kalman JM, Winship I, Vohra JK.

Heart Rhythm. 2013 Nov;10(11):1653-60. doi: 10.1016/j.hrthm.2013.08.022. Epub 2013 Aug 22.

PMID:
23973953
6.

Family letters are an effective way to inform relatives about inherited cardiac disease.

van der Roest WP, Pennings JM, Bakker M, van den Berg MP, van Tintelen JP.

Am J Med Genet A. 2009 Mar;149A(3):357-63. doi: 10.1002/ajmg.a.32672.

PMID:
19213028
7.

A comparison of genetic findings in sudden cardiac death victims and cardiac patients: the importance of phenotypic classification.

Hertz CL, Ferrero-Miliani L, Frank-Hansen R, Morling N, Bundgaard H.

Europace. 2015 Mar;17(3):350-7. doi: 10.1093/europace/euu210. Epub 2014 Oct 26. Review.

PMID:
25345827
8.

Cardiac evaluation of pediatric relatives in sudden arrhythmic death syndrome: a 2-center experience.

Wong LC, Roses-Noguer F, Till JA, Behr ER.

Circ Arrhythm Electrophysiol. 2014 Oct;7(5):800-6. doi: 10.1161/CIRCEP.114.001818. Epub 2014 Sep 6.

PMID:
25194972
9.

The Genetic Counselor in the Pediatric Arrhythmia Clinic: Review and Assessment of Services.

Helm BM, Freeze SL, Spoonamore KG, Ware SM, Ayers MD, Kean AC.

J Genet Couns. 2018 Jun;27(3):558-564. doi: 10.1007/s10897-017-0169-5. Epub 2017 Oct 27. Review.

PMID:
29079892
10.

Hereditary arrhythmias and cardiomyopathies: decision-making about genetic testing.

Louis C, Calamaro E, Vinocur JM.

Curr Opin Cardiol. 2018 Jan;33(1):78-86. doi: 10.1097/HCO.0000000000000477. Review.

PMID:
29059074
11.

Patient Outcomes From a Specialized Inherited Arrhythmia Clinic.

Adler A, Sadek MM, Chan AY, Dell E, Rutberg J, Davis D, Green MS, Spears DA, Gollob MH.

Circ Arrhythm Electrophysiol. 2016 Jan;9(1):e003440. doi: 10.1161/CIRCEP.115.003440.

PMID:
26743238
12.

Implantable defibrillators in long QT syndrome, Brugada syndrome, hypertrophic cardiomyopathy, and arrhythmogenic right ventricular cardiomyopathy.

Dohadwala M, Link MS.

Cardiol Clin. 2014 May;32(2):305-18. doi: 10.1016/j.ccl.2013.11.003. Epub 2014 Jan 23. Review.

PMID:
24793806
13.

Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.

Allegue C, Gil R, Blanco-Verea A, Santori M, Rodríguez-Calvo M, Concheiro L, Carracedo A, Brion M.

Int J Legal Med. 2011 Jul;125(4):565-72. doi: 10.1007/s00414-011-0572-7. Epub 2011 Apr 16.

PMID:
21499742
14.

Sudden cardiac death with autopsy findings of uncertain significance: potential for erroneous interpretation.

Papadakis M, Raju H, Behr ER, De Noronha SV, Spath N, Kouloubinis A, Sheppard MN, Sharma S.

Circ Arrhythm Electrophysiol. 2013 Jun;6(3):588-96. doi: 10.1161/CIRCEP.113.000111. Epub 2013 May 13. Erratum in: Circ Arrhythm Electrophysiol. 2013 Aug;6(4):e67.

PMID:
23671135
15.

Uptake of genetic counselling and predictive DNA testing in hypertrophic cardiomyopathy.

Christiaans I, Birnie E, Bonsel GJ, Wilde AA, van Langen IM.

Eur J Hum Genet. 2008 Oct;16(10):1201-7. doi: 10.1038/ejhg.2008.92. Epub 2008 May 14.

16.

Practice Variation among an International Group of Genetic Counselors on when to Offer Predictive Genetic Testing to Children at Risk of an Inherited Arrhythmia or Cardiomyopathy.

Christian S, Somerville M, Huculak C, Atallah J.

J Genet Couns. 2018 Aug 21. doi: 10.1007/s10897-018-0293-x. [Epub ahead of print]

PMID:
30132189
17.

Genetic testing and genetic counseling in patients with sudden death risk due to heritable arrhythmias.

Spoonamore KG, Ware SM.

Heart Rhythm. 2016 Mar;13(3):789-97. doi: 10.1016/j.hrthm.2015.11.013. Epub 2015 Nov 12. Review.

PMID:
26582592
18.

Clinical Presentation of Pediatric Patients at Risk for Sudden Cardiac Arrest.

Dalal A, Czosek RJ, Kovach J, von Alvensleben JC, Valdes S, Etheridge SP, Ackerman MJ, Auld D, Huckaby J, McCracken C, Campbell R.

J Pediatr. 2016 Oct;177:191-196. doi: 10.1016/j.jpeds.2016.06.088. Epub 2016 Aug 5.

PMID:
27502104
19.

Sudden cardiac arrest in the young due to inherited arrhythmias: the importance of family care.

Vincent GM.

Pacing Clin Electrophysiol. 2009 Jul;32 Suppl 2:S19-22. doi: 10.1111/j.1540-8159.2009.02395.x. Review.

PMID:
19602157
20.

Interpreting secondary cardiac disease variants in an exome cohort.

Ng D, Johnston JJ, Teer JK, Singh LN, Peller LC, Wynter JS, Lewis KL, Cooper DN, Stenson PD, Mullikin JC, Biesecker LG; NIH Intramural Sequencing Center (NISC) Comparative Sequencing Program.

Circ Cardiovasc Genet. 2013 Aug;6(4):337-46. doi: 10.1161/CIRCGENETICS.113.000039. Epub 2013 Jul 16.

Supplemental Content

Support Center