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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

363 related items for PubMed ID: 25500949

  • 1. Post-mortem Whole exome sequencing with gene-specific analysis for autopsy-negative sudden unexplained death in the young: a case series.
    Narula N, Tester DJ, Paulmichl A, Maleszewski JJ, Ackerman MJ.
    Pediatr Cardiol; 2015 Apr; 36(4):768-78. PubMed ID: 25500949
    [Abstract] [Full Text] [Related]

  • 2. 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; 9(3):259-65. PubMed ID: 27114410
    [Abstract] [Full Text] [Related]

  • 3. Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases.
    Neubauer J, Haas C, Bartsch C, Medeiros-Domingo A, Berger W.
    Int J Legal Med; 2016 Jul; 130(4):1011-1021. PubMed ID: 26846766
    [Abstract] [Full Text] [Related]

  • 4. Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes.
    Neubauer J, Lecca MR, Russo G, Bartsch C, Medeiros-Domingo A, Berger W, Haas C.
    Int J Legal Med; 2018 Jul; 132(4):1057-1065. PubMed ID: 29350269
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the Young.
    Sutphin BS, Boczek NJ, Barajas-Martínez H, Hu D, Ye D, Tester DJ, Antzelevitch C, Ackerman MJ.
    Congenit Heart Dis; 2016 Dec; 11(6):683-692. PubMed ID: 27218670
    [Abstract] [Full Text] [Related]

  • 7. Exome analysis-based molecular autopsy in cases of sudden unexplained death in the young.
    Bagnall RD, Das K J, Duflou J, Semsarian C.
    Heart Rhythm; 2014 Apr; 11(4):655-62. PubMed ID: 24440382
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome.
    Suktitipat B, Sathirareuangchai S, Roothumnong E, Thongnoppakhun W, Wangkiratikant P, Vorasan N, Krittayaphong R, Pithukpakorn M, Boonyapisit W.
    PLoS One; 2017 Apr; 12(7):e0180056. PubMed ID: 28704380
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Re-analysis of whole-exome sequencing data uncovers novel diagnostic variants and improves molecular diagnostic yields for sudden death and idiopathic diseases.
    Salfati EL, Spencer EG, Topol SE, Muse ED, Rueda M, Lucas JR, Wagner GN, Campman S, Topol EJ, Torkamani A.
    Genome Med; 2019 Dec 17; 11(1):83. PubMed ID: 31847883
    [Abstract] [Full Text] [Related]

  • 17. Targeted 46-gene and clinical exome sequencing for mutations causing cardiomyopathies.
    Waldmüller S, Schroeder C, Sturm M, Scheffold T, Imbrich K, Junker S, Frische C, Hofbeck M, Bauer P, Bonin M, Gawaz M, Gramlich M.
    Mol Cell Probes; 2015 Oct 17; 29(5):308-14. PubMed ID: 25979592
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Exome Sequencing Highlights a Potential Role for Concealed Cardiomyopathies in Youthful Sudden Cardiac Death.
    Neves R, Tester DJ, Simpson MA, Behr ER, Ackerman MJ, Giudicessi JR.
    Circ Genom Precis Med; 2022 Feb 17; 15(1):e003497. PubMed ID: 34949102
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 19.