These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 21955955)

  • 1. Challenges of genetic testing in adolescents with cardiac arrhythmia syndromes.
    Cohen LL; Stolerman M; Walsh C; Wasserman D; Dolan SM
    J Med Ethics; 2012 Mar; 38(3):163-7. PubMed ID: 21955955
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Disclosing Genetic Information to Family Members About Inherited Cardiac Arrhythmias: An Obligation or a Choice?
    Vavolizza RD; Kalia I; Erskine Aaron K; Silverstein LB; Barlevy D; Wasserman D; Walsh C; Marion RW; Dolan SM
    J Genet Couns; 2015 Aug; 24(4):608-15. PubMed ID: 25400212
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Explaining sudden infant death with cardiac arrhythmias: Complete exon sequencing of nine cardiac arrhythmia genes in Dutch SIDS cases highlights new and known DNA variants.
    Liebrechts-Akkerman G; Liu F; van Marion R; Dinjens WNM; Kayser M
    Forensic Sci Int Genet; 2020 May; 46():102266. PubMed ID: 32145446
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 128(14):1513-21. PubMed ID: 23963746
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cardiac ion channel mutations in the sudden infant death syndrome.
    Klaver EC; Versluijs GM; Wilders R
    Int J Cardiol; 2011 Oct; 152(2):162-70. PubMed ID: 21215473
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Medullary thyroid carcinoma: ethical issues for the surgeon.
    Shuman AG; Shaha AR; Tuttle RM; Fins JJ; Morris LG
    Ann Surg Oncol; 2012 Jul; 19(7):2102-7. PubMed ID: 22322952
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic analysis of sudden unexplained death: a multidisciplinary approach.
    Kauferstein S; Kiehne N; Jenewein T; Biel S; Kopp M; König R; Erkapic D; Rothschild M; Neumann T
    Forensic Sci Int; 2013 Jun; 229(1-3):122-7. PubMed ID: 23683917
    [TBL] [Abstract][Full Text] [Related]  

  • 8. American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.
    American Society of Clinical Oncology
    J Clin Oncol; 2003 Jun; 21(12):2397-406. PubMed ID: 12692171
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
    Antzelevitch C
    J Electrocardiol; 2001; 34 Suppl():177-81. PubMed ID: 11781953
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ethical, legal, and counseling challenges surrounding the return of genetic results in oncology.
    Lolkema MP; Gadellaa-van Hooijdonk CG; Bredenoord AL; Kapitein P; Roach N; Cuppen E; Knoers NV; Voest EE
    J Clin Oncol; 2013 May; 31(15):1842-8. PubMed ID: 23589552
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Professional and personal attitudes about access and confidentiality in the genetic testing of children: a pilot study.
    Campbell E; Ross LF
    Genet Test; 2003; 7(2):123-30. PubMed ID: 12885333
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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. PubMed ID: 25194972
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cardiac channelopathies and sudden infant death syndrome.
    Tfelt-Hansen J; Winkel BG; Grunnet M; Jespersen T
    Cardiology; 2011; 119(1):21-33. PubMed ID: 21778721
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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. PubMed ID: 19602157
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Privacy and disclosure in medical genetics examined in an ethics of care.
    Wertz DC; Fletcher JC
    Bioethics; 1991 Jul; 5(3):212-32. PubMed ID: 11659340
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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. PubMed ID: 26582592
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ethical Considerations on Pediatric Genetic Testing Results in Electronic Health Records.
    Kanungo S; Barr J; Crutchfield P; Fealko C; Soares N
    Appl Clin Inform; 2020 Oct; 11(5):755-763. PubMed ID: 33176390
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Emerging Implications of Genetic Testing in Inherited Primary Arrhythmia Syndromes.
    Asatryan B; Medeiros-Domingo A
    Cardiol Rev; 2019; 27(1):23-33. PubMed ID: 29528859
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The sudden infant death syndrome gene: does it exist?
    Opdal SH; Rognum TO
    Pediatrics; 2004 Oct; 114(4):e506-12. PubMed ID: 15466077
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Social and family considerations in genetic counselling].
    Svendsen MN; Koch L
    Ugeskr Laeger; 2006 Jun; 168(24):2348-50. PubMed ID: 16822418
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.