BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 30354306)

  • 21. AHA assesses the impact of genotyping on diagnosis of genetic cardiac disease. American Heart Association.
    Morey SS
    Am Fam Physician; 1999 May; 59(10):2915-6, 2918. PubMed ID: 10348078
    [No Abstract]   [Full Text] [Related]  

  • 22. Multiplex targeted high-throughput sequencing for Mendelian cardiac disorders.
    Fokstuen S; Makrythanasis P; Nikolaev S; Santoni F; Robyr D; Munoz A; Bevillard J; Farinelli L; Iseli C; Antonarakis SE; Blouin JL
    Clin Genet; 2014 Apr; 85(4):365-70. PubMed ID: 23590259
    [TBL] [Abstract][Full Text] [Related]  

  • 23. QT dispersion in alpha-myosin heavy-chain familial hypertrophic cardiomyopathy mice.
    Bevilacqua LM; Maguire CT; Seidman JG; Seidman CE; Berul CI
    Pediatr Res; 1999 May; 45(5 Pt 1):643-7. PubMed ID: 10231857
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Using whole exome sequencing to walk from clinical practice to research and back again.
    Schuler BA; Prisco SZ; Jacob HJ
    Circulation; 2013 Mar; 127(9):968-70. PubMed ID: 23388216
    [No Abstract]   [Full Text] [Related]  

  • 25. Impediments to DNA testing and cascade screening for hypertrophic cardiomyopathy and Long QT syndrome: a qualitative study of patient experiences.
    Smart A
    J Genet Couns; 2010 Dec; 19(6):630-9. PubMed ID: 20680418
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic testing for inherited cardiac arrhythmias.
    Fowler SJ; Cerrone M; Napolitano C; Priori SG
    Hellenic J Cardiol; 2010; 51(2):92-103. PubMed ID: 20378510
    [No Abstract]   [Full Text] [Related]  

  • 27. The role of genetic testing in paediatric syndromes of sudden death: state of the art and future considerations.
    McCormack J
    Cardiol Young; 2009 Nov; 19 Suppl 2():54-65. PubMed ID: 19857351
    [No Abstract]   [Full Text] [Related]  

  • 28. 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]  

  • 29. Molecular biology of heart disease. Synopsis of the pathophysiological basis of cardiac hypertrophy, familial hypertrophic cardiomyopathy, long QT syndrome and Marfan syndrome.
    Kurabayashi M; Yazaki Y
    Intern Med; 1996 Apr; 35(4):243-8. PubMed ID: 8739775
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Molecular genetics of cardiovascular diseases].
    Schunkert H; Hense HW
    Dtsch Med Wochenschr; 1995 Apr; 120(15):533-9. PubMed ID: 7720536
    [No Abstract]   [Full Text] [Related]  

  • 31. Peripartum cardiomyopathy presenting with syncope due to Torsades de pointes: a case of long QT syndrome with a novel KCNH2 mutation.
    Nishimoto O; Matsuda M; Nakamoto K; Nishiyama H; Kuraoka K; Taniyama K; Tamura R; Shimizu W; Kawamoto T
    Intern Med; 2012; 51(5):461-4. PubMed ID: 22382559
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Neonatal long QT syndrome due to a de novo dominant negative hERG mutation.
    Beery TA; Shooner KA; Benson DW
    Am J Crit Care; 2007 Jul; 16(4):416, 412-5. PubMed ID: 17595376
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A new role for calmodulin in ion channel biology.
    Roden DM
    Circ Res; 2006 Apr; 98(8):979-81. PubMed ID: 16645144
    [No Abstract]   [Full Text] [Related]  

  • 34. Post-mortem genetic testing in a family with long-QT syndrome and hypertrophic cardiomyopathy.
    Kane DA; Triedman J
    Cardiovasc Pathol; 2014; 23(2):107-9. PubMed ID: 24322056
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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. PubMed ID: 24793806
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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. PubMed ID: 28566242
    [TBL] [Abstract][Full Text] [Related]  

  • 37. NOS1AP Polymorphisms Modify QTc Interval Duration But Not Cardiac Arrest Risk in Hypertrophic Cardiomyopathy.
    Earle N; Ingles J; Bagnall RD; Gray B; Crawford J; Smith W; Shelling AN; Love DR; Semsarian C; Skinner JR
    J Cardiovasc Electrophysiol; 2015 Dec; 26(12):1346-51. PubMed ID: 26332198
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Long QT syndrome in extensive infective endocarditis complicating hypertrophic obstructive cardiomyopathy.
    Yuan SM; Demesthenous E; Coman V
    Kardiol Pol; 2009 Jan; 67(1):53-7. PubMed ID: 19253191
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetics of cardiovascular disease.
    Cymet T
    Compr Ther; 2010; 36():18-9. PubMed ID: 21229815
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetics and cardiovascular disease.
    Allen JK
    Nurs Clin North Am; 2000 Sep; 35(3):653-62. PubMed ID: 10957680
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.