Niimura H - Search Results

1

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. Niimura H, et al. N Engl J Med. 1998 Apr 30;338(18):1248-57. doi: 10.1056/NEJM199804303381802. N Engl J Med. 1998. PMID: 9562578 Free article.

2

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly.

Niimura H, Patton KK, McKenna WJ, Soults J, Maron BJ, Seidman JG, Seidman CE. Niimura H, et al. Circulation. 2002 Jan 29;105(4):446-51. doi: 10.1161/hc0402.102990. Circulation. 2002. PMID: 11815426

3

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice.

McConnell BK, Jones KA, Fatkin D, Arroyo LH, Lee RT, Aristizabal O, Turnbull DH, Georgakopoulos D, Kass D, Bond M, Niimura H, Schoen FJ, Conner D, Fischman DA, Seidman CE, Seidman JG. McConnell BK, et al. Among authors: niimura h. J Clin Invest. 1999 Nov;104(9):1235-44. doi: 10.1172/JCI7377. J Clin Invest. 1999. PMID: 10545522 Free PMC article.

4

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, Solomon S, Benson DW, Seidman JG, Seidman CE. Siu BL, et al. Among authors: niimura h. Circulation. 1999 Mar 2;99(8):1022-6. doi: 10.1161/01.cir.99.8.1022. Circulation. 1999. PMID: 10051295

5

Development of left ventricular hypertrophy in adults in hypertrophic cardiomyopathy caused by cardiac myosin-binding protein C gene mutations.

Maron BJ, Niimura H, Casey SA, Soper MK, Wright GB, Seidman JG, Seidman CE. Maron BJ, et al. Among authors: niimura h. J Am Coll Cardiol. 2001 Aug;38(2):315-21. doi: 10.1016/s0735-1097(01)01386-9. J Am Coll Cardiol. 2001. PMID: 11499718 Free article.

6

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice.

McConnell BK, Jones KA, Fatkin D, Arroyo LH, Lee RT, Aristizabal O, Turnbull DH, Georgakopoulos D, Kass D, Bond M, Niimura H, Schoen FJ, Conner D, Fischman DA, Seidman CE, Seidman JG. McConnell BK, et al. Among authors: niimura h. J Clin Invest. 1999 Dec;104(12):1771. doi: 10.1172/jci7377c1. J Clin Invest. 1999. PMID: 10606631 Free PMC article. No abstract available.

7

A novel deletion mutation in the cardiac myosin-binding protein C gene as a cause of Maron's type IV hypertrophic cardiomyopathy.

Anan R, Niimura H, Minagoe S, Tei C. Anan R, et al. Among authors: niimura h. Am J Cardiol. 2002 Feb 15;89(4):487-8. doi: 10.1016/s0002-9149(01)02281-0. Am J Cardiol. 2002. PMID: 11835941 No abstract available.

8

Mutations in the genes for sarcomeric proteins in Japanese patients with onset sporadic hypertrophic cardiomyopathy after age 40 years.

Anan R, Niimura H, Takenaka T, Hamasaki S, Tei C. Anan R, et al. Among authors: niimura h. Am J Cardiol. 2007 Jun 15;99(12):1750-4. doi: 10.1016/j.amjcard.2007.01.066. Epub 2007 Apr 26. Am J Cardiol. 2007. PMID: 17560888

9

[Genotype-phenotype correlations in familial hypertrophic cardiomyopathy].

Anan R, Niimura H, Tei C. Anan R, et al. Among authors: niimura h. Nihon Rinsho. 2000 Jan;58(1):134-40. Nihon Rinsho. 2000. PMID: 10885301 Review. Japanese.

10

Image in clinical medicine. Coronary-artery fistula with a giant aneurysm.

Niimura H, Tei C. Niimura H, et al. N Engl J Med. 2002 Apr 18;346(16):1211. doi: 10.1056/NEJMicm000094. N Engl J Med. 2002. PMID: 11961150 Free article. No abstract available.

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