PubMed (OMIM) for id: 104705

Year	Number of Results
1958	1
1961	1
1963	1
1964	1
1965	1
1966	1
1967	1
1968	1
1973	3
1974	1
1975	1
1976	2
1977	1
1979	3
1980	1
1981	1
1982	3
1983	2
1985	3
1986	1
1987	3
1989	3
1990	3
1991	2
1992	3
1993	1
1994	1
1996	2
1997	1
1998	1
1999	2
2000	5
2001	3
2002	2
2003	4
2004	1
2023	0

1

Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy.

Tsybouleva N, Zhang L, Chen S, Patel R, Lutucuta S, Nemoto S, DeFreitas G, Entman M, Carabello BA, Roberts R, Marian AJ. Tsybouleva N, et al. Circulation. 2004 Mar 16;109(10):1284-91. doi: 10.1161/01.CIR.0000121426.43044.2B. Epub 2004 Mar 1. Circulation. 2004. PMID: 14993121 Free PMC article.

2

IDIOPATHIC HYPERTROPHIC SUBAORTIC STENOSIS. I. A DESCRIPTION OF THE DISEASE BASED UPON AN ANALYSIS OF 64 PATIENTS.

BRAUNWALD E, LAMBREW CT, ROCKOFF SD, ROSS J Jr, MORROW AG. BRAUNWALD E, et al. Circulation. 1964 Nov;30:SUPPL 4:3-119. doi: 10.1161/01.cir.29.5s4.iv-3. Circulation. 1964. PMID: 14227306 No abstract available.

3

Muscular subaortic stenosis.

MANCHESTER GH. MANCHESTER GH. N Engl J Med. 1963 Aug 8;269:300-6. doi: 10.1056/NEJM196308082690606. N Engl J Med. 1963. PMID: 13932709 No abstract available.

4

Hereditary cardiovascular dysplasia. A form of familial cardiomyopathy.

PARE JA, FRASER RG, PIROZYNSKI WJ, SHANKS JA, STUBINGTON D. PARE JA, et al. Am J Med. 1961 Jul;31:37-62. doi: 10.1016/0002-9343(61)90222-4. Am J Med. 1961. PMID: 13732753 No abstract available.

5

Asymmetrical hypertrophy of the heart in young adults.

TEARE D. TEARE D. Br Heart J. 1958 Jan;20(1):1-8. doi: 10.1136/hrt.20.1.1. Br Heart J. 1958. PMID: 13499764 Free PMC article. No abstract available.

6

Mutation spectrum in a large cohort of unrelated consecutive patients with hypertrophic cardiomyopathy.

Erdmann J, Daehmlow S, Wischke S, Senyuva M, Werner U, Raible J, Tanis N, Dyachenko S, Hummel M, Hetzer R, Regitz-Zagrosek V. Erdmann J, et al. Clin Genet. 2003 Oct;64(4):339-49. doi: 10.1034/j.1399-0004.2003.00151.x. Clin Genet. 2003. PMID: 12974739

7

Sudden death in young athletes.

Maron BJ. Maron BJ. N Engl J Med. 2003 Sep 11;349(11):1064-75. doi: 10.1056/NEJMra022783. N Engl J Med. 2003. PMID: 12968091 Review. No abstract available.

8

Assessing risk in hypertrophic cardiomyopathy.

Cannon RO 3rd. Cannon RO 3rd. N Engl J Med. 2003 Sep 11;349(11):1016-8. doi: 10.1056/NEJMp038122. N Engl J Med. 2003. PMID: 12968084 No abstract available.

9

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

Taylor RW, Giordano C, Davidson MM, d'Amati G, Bain H, Hayes CM, Leonard H, Barron MJ, Casali C, Santorelli FM, Hirano M, Lightowlers RN, DiMauro S, Turnbull DM. Taylor RW, et al. J Am Coll Cardiol. 2003 May 21;41(10):1786-96. doi: 10.1016/s0735-1097(03)00300-0. J Am Coll Cardiol. 2003. PMID: 12767666 Free article.

10

Phenotypic diversity in hypertrophic cardiomyopathy.

Arad M, Seidman JG, Seidman CE. Arad M, et al. Hum Mol Genet. 2002 Oct 1;11(20):2499-506. doi: 10.1093/hmg/11.20.2499. Hum Mol Genet. 2002. PMID: 12351586 Review.

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