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 *

130 related articles for article (PubMed ID: 11424919)

  • 21. A previously undescribed de novo insertion-deletion mutation in the beta myosin heavy chain gene in a kindred with familial hypertrophic cardiomyopathy.
    Cuda G; Perrotti N; Perticone F; Mattioli PL
    Heart; 1996 Nov; 76(5):451-2. PubMed ID: 8944596
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Hypertrophic cardiomyopathy and left ventricular non-compaction: Different manifestations of the same cardiomyopathy spectrum?
    Lorca R; Martín M; Gómez J; Santamarta E; Morís C; Reguero JJ; Coto E
    Int J Cardiol; 2015; 190():26-8. PubMed ID: 25912113
    [No Abstract]   [Full Text] [Related]  

  • 23. [Fabry disease among hypertrophic cardiomyopathy of genetic origin].
    Bouvagnet P; Millat G; Rousson R; Gilbert G; Derumeaux G
    Rev Med Interne; 2010 Dec; 31 Suppl 2():S233-7. PubMed ID: 21211671
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy.
    Chida A; Inai K; Sato H; Shimada E; Nishizawa T; Shimada M; Furutani M; Furutani Y; Kawamura Y; Sugimoto M; Ishihara J; Fujiwara M; Soga T; Kawana M; Fuji S; Tateno S; Kuraishi K; Kogaki S; Nishimura M; Ayusawa M; Ichida F; Yamazawa H; Matsuoka R; Nonoyama S; Nakanishi T
    Heart Vessels; 2017 Jun; 32(6):700-707. PubMed ID: 27885498
    [TBL] [Abstract][Full Text] [Related]  

  • 25. New Variant With a Previously Unrecognized Mechanism of Pathogenicity in Hypertrophic Cardiomyopathy.
    Aguib Y; Allouba M; Walsh R; Ibrahim AM; Halawa S; Afify A; Hosny M; Theotokis PI; Galal A; Elshorbagy S; Roshdy M; Kassem HS; Ellithy A; Buchan R; Whiffin N; Anwer S; Cook SA; Moustafa A; ElGuindy A; Ware JS; Barton PJR; Yacoub M
    Circulation; 2021 Aug; 144(9):754-757. PubMed ID: 34460321
    [No Abstract]   [Full Text] [Related]  

  • 26. Clinical outcomes associated with sarcomere mutations in hypertrophic cardiomyopathy: a meta-analysis on 7675 individuals.
    Sedaghat-Hamedani F; Kayvanpour E; Tugrul OF; Lai A; Amr A; Haas J; Proctor T; Ehlermann P; Jensen K; Katus HA; Meder B
    Clin Res Cardiol; 2018 Jan; 107(1):30-41. PubMed ID: 28840316
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Beta-myosin heavy chain gene mutations and hypertrophic cardiomyopathy in Austrian children.
    Greber-Platzer S; Marx M; Fleischmann C; Suppan C; Dobner M; Wimmer M
    J Mol Cell Cardiol; 2001 Jan; 33(1):141-8. PubMed ID: 11133230
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A molecular screening strategy based on beta-myosin heavy chain, cardiac myosin binding protein C and troponin T genes in Italian patients with hypertrophic cardiomyopathy.
    Girolami F; Olivotto I; Passerini I; Zachara E; Nistri S; Re F; Fantini S; Baldini K; Torricelli F; Cecchi F
    J Cardiovasc Med (Hagerstown); 2006 Aug; 7(8):601-7. PubMed ID: 16858239
    [TBL] [Abstract][Full Text] [Related]  

  • 29. New concepts in hypertrophic cardiomyopathies, part I.
    Roberts R; Sigwart U
    Circulation; 2001 Oct; 104(17):2113-6. PubMed ID: 11673355
    [No Abstract]   [Full Text] [Related]  

  • 30. Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene.
    Andersen PS; Havndrup O; Bundgaard H; Larsen LA; Vuust J; Kjeldsen K; Christiansen M
    Clin Genet; 1999 Sep; 56(3):244-6. PubMed ID: 10563488
    [No Abstract]   [Full Text] [Related]  

  • 31. Detection of mutations in symptomatic patients with hypertrophic cardiomyopathy in Taiwan.
    Chiou KR; Chu CT; Charng MJ
    J Cardiol; 2015 Mar; 65(3):250-6. PubMed ID: 25086479
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mutations of the beta myosin heavy chain gene in hypertrophic cardiomyopathy: critical functional sites determine prognosis.
    Woo A; Rakowski H; Liew JC; Zhao MS; Liew CC; Parker TG; Zeller M; Wigle ED; Sole MJ
    Heart; 2003 Oct; 89(10):1179-85. PubMed ID: 12975413
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain.
    Bundgaard H; Havndrup O; Andersen PS; Larsen LA; Brandt NJ; Vuust J; Kjeldsen K; Christiansen M
    J Mol Cell Cardiol; 1999 Apr; 31(4):745-50. PubMed ID: 10329202
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Familial hypertrophic cardiomyopathy: man, mouse and cat.
    Baty C; Watkins H
    QJM; 1998 Dec; 91(12):791-3. PubMed ID: 10024943
    [No Abstract]   [Full Text] [Related]  

  • 35. [Two cases of diagnosis of family hypertrophic cardiomyopathy].
    Erov NK; Kretov AF; Kochube'i GI
    Ter Arkh; 1999; 71(4):35-6. PubMed ID: 10358860
    [No Abstract]   [Full Text] [Related]  

  • 36. Dextrocardia and symmetric hypertrophic cardiomyopathy with multiple mutations of genes encoding the sarcomere proteins.
    Fang F; Cui FM; He YM; Yang XJ; Zhao X; Xu HF; Yu CM
    Int J Cardiol; 2015; 187():581-4. PubMed ID: 25863306
    [No Abstract]   [Full Text] [Related]  

  • 37. Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy.
    Carniel E; Taylor MR; Sinagra G; Di Lenarda A; Ku L; Fain PR; Boucek MM; Cavanaugh J; Miocic S; Slavov D; Graw SL; Feiger J; Zhu XZ; Dao D; Ferguson DA; Bristow MR; Mestroni L
    Circulation; 2005 Jul; 112(1):54-9. PubMed ID: 15998695
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.
    Selvi Rani D; Nallari P; Dhandapany PS; Rani J; Meraj K; Ganesan M; Narasimhan C; Thangaraj K
    DNA Cell Biol; 2015 May; 34(5):350-9. PubMed ID: 25607779
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Screening of MYH7, MYBPC3, and TNNT2 genes in Brazilian patients with hypertrophic cardiomyopathy.
    Marsiglia JD; Credidio FL; de Oliveira TG; Reis RF; Antunes Mde O; de Araujo AQ; Pedrosa RP; Barbosa-Ferreira JM; Mady C; Krieger JE; Arteaga-Fernandez E; Pereira Ada C
    Am Heart J; 2013 Oct; 166(4):775-82. PubMed ID: 24093860
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Familial hypertrophic cardiomyopathy: the same mutation, different prognosis. Comparison of two families with a long follow-up.
    Brito D; Richard P; Isnard R; Pipa J; Komajda M; Madeira H
    Rev Port Cardiol; 2003 Dec; 22(12):1445-61. PubMed ID: 15008060
    [TBL] [Abstract][Full Text] [Related]  

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