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Journal Abstract Search
200 related items for PubMed ID: 11877825
1. [Sarcomere gene mutations--a cause of hypertrophic cardiomyopathy]. Kuusisto J, Jääskeläinen P, Laakso M. Duodecim; 1999; 115(9):997-8. PubMed ID: 11877825 [No Abstract] [Full Text] [Related]
3. Molecular etiology of idiopathic cardiomyopathy in Asian populations. Kimura A, Ito-Satoh M, Hayashi T, Takahashi M, Arimura T. J Cardiol; 2001; 37 Suppl 1():139-46. PubMed ID: 11433818 [Abstract] [Full Text] [Related]
6. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes. Kaski JP, Syrris P, Burch M, Tomé-Esteban MT, Fenton M, Christiansen M, Andersen PS, Sebire N, Ashworth M, Deanfield JE, McKenna WJ, Elliott PM. Heart; 2008 Nov; 94(11):1478-84. PubMed ID: 18467357 [Abstract] [Full Text] [Related]
9. When the heart in trouble is a young one. Dulak SB. RN; 2006 May; 69(5):24ac1-5; quiz 24ac6. PubMed ID: 16722262 [No Abstract] [Full Text] [Related]
12. Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype. Kubo T, Gimeno JR, Bahl A, Steffensen U, Steffensen M, Osman E, Thaman R, Mogensen J, Elliott PM, Doi Y, McKenna WJ. J Am Coll Cardiol; 2007 Jun 26; 49(25):2419-26. PubMed ID: 17599605 [Abstract] [Full Text] [Related]
18. Novel locus for an inherited cardiomyopathy maps to chromosome 7. Song L, DePalma SR, Kharlap M, Zenovich AG, Cirino A, Mitchell R, McDonough B, Maron BJ, Seidman CE, Seidman JG, Ho CY. Circulation; 2006 May 09; 113(18):2186-92. PubMed ID: 16651466 [Abstract] [Full Text] [Related]