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.
27. Preclinical diagnosis of familial hypertrophic cardiomyopathy by genetic analysis of blood lymphocytes. Rosenzweig A; Watkins H; Hwang DS; Miri M; McKenna W; Traill TA; Seidman JG; Seidman CE N Engl J Med; 1991 Dec; 325(25):1753-60. PubMed ID: 1944483 [TBL] [Abstract][Full Text] [Related]
28. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. Niimura H; Bachinski LL; Sangwatanaroj S; Watkins H; Chudley AE; McKenna W; Kristinsson A; Roberts R; Sole M; Maron BJ; Seidman JG; Seidman CE N Engl J Med; 1998 Apr; 338(18):1248-57. PubMed ID: 9562578 [TBL] [Abstract][Full Text] [Related]
29. Fixed subaortic stenosis associated with hypertrophic cardiomyopathy: report of a rare familial occurrence. Conte MR; Bongioanni S; Dall'Orto G; Nicastro C; Bonfiglio G; Morello M; Mangiardi L; Brusca A G Ital Cardiol; 1998 Jan; 28(1):53-6. PubMed ID: 9493046 [TBL] [Abstract][Full Text] [Related]
30. Familial cardiomyopathy with variable hypertrophic and restrictive features and common HLA haplotype. Feld S; Caspi A Isr J Med Sci; 1992 May; 28(5):277-80. PubMed ID: 1597356 [TBL] [Abstract][Full Text] [Related]
31. [Familial hypertrophic cardiomyopathy]. Wróblewska-Kałuzewska M; Ozimek W; Pleskot M; Jedrasik P Pol Merkur Lekarski; 1997 Feb; 2(8):129-31. PubMed ID: 9538659 [TBL] [Abstract][Full Text] [Related]
32. [Critical study of the criteria of diagnosis of hypertrophic subvalvular aortic stenosis by TM echocardiography (author's transl)]. Lemoine C; Neimann JL Ann Cardiol Angeiol (Paris); 1980; 29(3):147-53. PubMed ID: 7192530 [No Abstract] [Full Text] [Related]
33. [Hypertrophic obstructive cardiomyopathy-trimepranol-induced haemodynamic changes (author's transl)]. Jebavý P; Gebauerová M; Beránek I Cas Lek Cesk; 1982 Feb; 121(7):198-205. PubMed ID: 6122504 [No Abstract] [Full Text] [Related]
34. Clinical features of hypertrophic cardiomyopathy caused by an Arg278Cys missense mutation in the cardiac troponin T gene. Theopistou A; Anastasakis A; Miliou A; Rigopoulos A; Toutouzas P; Stefanadis C Am J Cardiol; 2004 Jul; 94(2):246-9. PubMed ID: 15246915 [TBL] [Abstract][Full Text] [Related]
35. Left ventricular outflow tract obstruction as a primary phenotypic expression of hypertrophic cardiomyopathy in mutation carriers without hypertrophy. Lopes LR; Cotrim C; Cruz I; Picano E; Pinto F; Pereira H Int J Cardiol; 2014 Oct; 176(3):1264-7. PubMed ID: 25127965 [No Abstract] [Full Text] [Related]
36. 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]
37. 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]