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Journal Abstract Search

467 related items for PubMed ID: 32145446

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
    Allegue C, Coll M, Mates J, Campuzano O, Iglesias A, Sobrino B, Brion M, Amigo J, Carracedo A, Brugada P, Brugada J, Brugada R.
    PLoS One; 2015 May; 10(7):e0133037. PubMed ID: 26230511
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  • 3. Targeted next generation sequencing application in cardiac channelopathies: Analysis of a cohort of autopsy-negative sudden unexplained deaths.
    Farrugia A, Keyser C, Hollard C, Raul JS, Muller J, Ludes B.
    Forensic Sci Int; 2015 Sep; 254():5-11. PubMed ID: 26164358
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  • 4. Post-mortem genetic investigation of cardiac disease-associated genes in sudden infant death syndrome (SIDS) cases.
    Köffer J, Scheiper-Welling S, Verhoff MA, Bajanowski T, Kauferstein S.
    Int J Legal Med; 2021 Jan; 135(1):207-212. PubMed ID: 32789579
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  • 5. Postmortem molecular analysis of KCNQ1, KCNH2, KCNE1 and KCNE2 genes in sudden unexplained nocturnal death syndrome in the Chinese Han population.
    Liu C, Zhao Q, Su T, Tang S, Lv G, Liu H, Quan L, Cheng J.
    Forensic Sci Int; 2013 Sep 10; 231(1-3):82-7. PubMed ID: 23890619
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  • 6. Application of Multigene Panel Sequencing in Patients with Prolonged Rate-corrected QT Interval and No Pathogenic Variants Detected in KCNQ1, KCNH2, and SCN5A.
    Seo SH, Kim SY, Cho SI, Park H, Lee S, Choi JM, Kim MJ, Lee JS, Ahn KJ, Song MK, Bae EJ, Park SS, Seong MW.
    Ann Lab Med; 2018 Jan 10; 38(1):54-58. PubMed ID: 29071820
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  • 8. Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths.
    Wang D, Shah KR, Um SY, Eng LS, Zhou B, Lin Y, Mitchell AA, Nicaj L, Prinz M, McDonald TV, Sampson BA, Tang Y.
    Forensic Sci Int; 2014 Apr 10; 237():90-9. PubMed ID: 24631775
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  • 12. Common Variants in KCNE1, KCNH2, and SCN5A May Impact Cardiac Arrhythmia Risk.
    Vatta M, Truty R, Garcia J, Callis TE, Hatchell K, Rojahn S, Morales A, Aradhya S, Nussbaum R.
    Circ Genom Precis Med; 2021 Feb 10; 14(1):e003206. PubMed ID: 33517668
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  • 13. Feasibility of analysis of the SCN5A gene in paraffin embedded samples in sudden infant death cases at the Pretoria Medico-Legal Laboratory, South Africa.
    van Deventer BS, du Toit-Prinsloo L, van Niekerk C.
    Forensic Sci Med Pathol; 2018 Sep 10; 14(3):276-284. PubMed ID: 29907895
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  • 15. Investigating cardiac genetic background in sudden infant death syndrome (SIDS).
    Cazzato F, Coll M, Grassi S, Fernàndez-Falgueras A, Nogué-Navarro L, Iglesias A, Castellà J, Oliva A, Brugada R.
    Int J Legal Med; 2024 Nov 10; 138(6):2229-2237. PubMed ID: 38849547
    [Abstract] [Full Text] [Related]

  • 16. Long QT molecular autopsy in sudden infant death syndrome.
    Glengarry JM, Crawford J, Morrow PL, Stables SR, Love DR, Skinner JR.
    Arch Dis Child; 2014 Jul 10; 99(7):635-40. PubMed ID: 24596401
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  • 17. Variant frequencies of KCNQ1, KCNH2, and SCN5A in a Chinese inherited arrhythmia cohort and other disease cohorts undergoing genetic testing.
    Li X, Liu N, Bai R.
    Ann Hum Genet; 2020 Mar 10; 84(2):161-168. PubMed ID: 31696929
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  • 18. Postmortem Analysis of 4 Mutation Hotspots of KCNQ1, KCNH2, and SCN5A Genes in Sudden Unexplained Death in Southwest of China.
    Jia PL, Wang YB, Fu H, Huang WL, Zhong SR, Ma L, Li YH, Dong Y, Sun ZC, Yang L, Qu PF, Zhao S, Qu YQ, Xi YM, Wang SW, Tang X, Lei PP.
    Am J Forensic Med Pathol; 2018 Sep 10; 39(3):218-222. PubMed ID: 29851656
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  • 19. Whole-Exome Molecular Autopsy After Exertion-Related Sudden Unexplained Death in the Young.
    Anderson JH, Tester DJ, Will ML, Ackerman MJ.
    Circ Cardiovasc Genet; 2016 Jun 10; 9(3):259-65. PubMed ID: 27114410
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  • 20. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
    Antzelevitch C.
    J Electrocardiol; 2001 Jun 10; 34 Suppl():177-81. PubMed ID: 11781953
    [Abstract] [Full Text] [Related]

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