Septal wall thinning and systolic dysfunction in patients with hypertrophic cardiomyopathy caused by a cardiac troponin I gene mutation
Masami Shimizu(Kanazawa University), Hiroshi Mabuchi(Kanazawa University), Hideki Itoh(Shiga University of Medical Science), Kotaro Oe(Kanazawa University), Masato Yamaguchi(Jikei University School of Medicine), Taku Iwaki(Kanazawa University), Kenshi Hayashi(Kanazawa University), Kazuyasu Okeie(Kouseiren Takaoka Hospital), Tetsuo Konno(Kanazawa University), Hidekazu Ino(Kanazawa University), Mitsuru Nagata
Cited by 10
Related Papers
Increased High-Density Lipoprotein Levels Caused by a Common Cholesteryl-Ester Transfer Protein Gene Mutation
|New England Journal of Medicine|1990|865
Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins
|Nature|1989|465
Cardiac fibrosis in mice with hypertrophic cardiomyopathy is mediated by non-myocyte proliferation and requires Tgf-β
|Journal of Clinical Investigation|2010|440
T wave peak-to-end interval and QT dispersion in acquired long QT syndrome: a new index for arrhythmogenicity
|Clinical Science|2003|313
Idiopathic Pulmonary Fibrosis. Epidemiologic Approaches to Occupational Exposure
|American Journal of Respiratory and Critical Care Medicine|1994|269