[1]
|
Elliott P, Anderson R, Arbustini E, et al.Classification of the cardiomyopathies:a position statement from the european society of cardiology working group on myocardial and pericardial diseases[J].Eur Heart J, 2008, 29:270-276. |
[2]
|
Arbustini E, Narula N, Tavazzi L, et al.The MOGE(S) classification of cardiomyopathy for clinicians[J].J Am Coll Cardiol, 2014, 64:304-318. |
[3]
|
Marchesini M, Uguccioni L, Parisi R, et al.The role of cardiac magnetic resonance imaging in hypertrophic cardiomyopathy[J].Rev Cardiovasc Med, 2016, 17:57-64. |
[4]
|
Kwon DH, Setser RM, Popović ZB, et al.Association of myocardial fibrosis, electrocardiography and ventricular tachyarrhythmia in hypertrophic cardiomyopathy:a delayed contrast enhanced MRI study[J].Int J Cardiovasc Imaging, 2008, 24:617-625. |
[5]
|
Hinojar R, Varma N, Child N, et al.T1 mapping in discrimination of hypertrophic phenotypes:hypertensive heart disease and hypertrophic cardiomyopathy:findings from the international T1 multicenter cardiovascular magnetic resonance study[J].Circ Cardiovasc Imaging, 2015, 8:pii:e003285. |
[6]
|
Sado DM, White SK, Piechnik SK, et al.Identification and assessment of Anderson-Fabry disease by cardiovascular magnetic resonance noncontrast myocardial T1 mapping[J].Circ Cardiovasc Imaging, 2013, 6:392-398. |
[7]
|
Moon JC, Sachdev B, Elkington AG, et al.Gadolinium enhanced cardiovascular magnetic resonance in Anderson-Fabry disease.Evidence for a disease specific abnormality of the myocardial interstitium[J].Eur Heart J, 2003, 24:2151-2155. |
[8]
|
Maceira AM, Joshi J, Prasad SK, et al.Cardiovascular magnetic resonance in cardiac amyloidosis[J].Circulation, 2005, 111:186-193. |
[9]
|
Ellims AH, Iles LM, Ling LH, et al.A comprehensive evaluation of myocardial fibrosis in hypertrophic cardiomyopathy with cardiac magnetic resonance imaging:linking genotype with fibrotic phenotype[J].Eur Heart J Cardiovasc Imaging, 2014, 15:1108-1116. |
[10]
|
Gillies RJ, Kinahan PE, Hricak H.Radiomics:images are more than pictures, they are data[J].Radiology, 2016, 278:563-577. |
[11]
|
Sengupta PP, Huang YM, Bansal M, et al.Cognitive machine-learning algorithm for cardiac imaging:A pilot study for differentiating constrictive pericarditis from restrictive cardiomyopathy[J].Circ Cardiovasc Imaging, 2016, 9:pii:e004330. |
[12]
|
Baessler B, Luecke C, Lurz J.Cardiac MRI texture analysis of T1 and T2 maps in patients with infarctlike acute myocarditis[J].Radiology, 2018, 289:357-365. |
[13]
|
Teekakirikul P, Kelly MA, Rehm HL, et al.Inherited cardiomyopathies:molecular genetics and clinical genetic testing in the postgenomic era[J].J Mol Diagn, 2013, 15:158-170. |
[14]
|
Worman HJ, Bonne G."Laminopathies":A wide spectrum of human diseases[J].Exper Cell Res, 2007, 313:2121-2133. |
[15]
|
Berne P, Brugada J.Brugada syndrome 2012[J].Circ J, 2012, 76:1563-1571. |
[16]
|
Millat G, Chanavat V, Rousson R.Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathies[J].Clin Chim Acta, 2014, 433:266-271. |
[17]
|
Loman NJ, Misra RV, Dallman TJ, et al.Performance comparison of benchtop high throughput sequencing platforms[J].Nat Biotechnol, 2012, 30:434-439. |
[18]
|
Zhao Y, Feng Y, Zhang YM, et al.Targeted next-generation sequencing of candidate genes reveals novel mutations in patients with dilated cardiomyopathy[J].Int J Mol Med, 2015, 36:1479-1486. |
[19]
|
Bottillo I, D'Angelantonio D, Caputo V, et al.Molecular analysis of sarcomeric and non-sarcomeric genes in patients with hypertrophic cardiomyopathy[J].Gene, 2016, 577:227-235. |
[20]
|
Lu C, Wu W, Liu F, et al.Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequenc-ing technologies[J].J Transl Med, 2018, 16:241. |
[21]
|
Wu W, Lu CX, Wang YN, et al.Novel phenotype-genotype correlations of restrictive cardiomyopathy with myosin-binding protein C (MYBPC3) gene mutations tested by next-genera-tion sequencing[J].J Am Heart Assoc, 2015, 4:e001879 |
[22]
|
Ruan YP, Lu CX, Zhao XY, et al.Restrictive Card-iomyopathy Resulting from a Troponin I Type 3 Mutation in a Chinese Family[J].Chin Med Sci J, 2016, 31:1-7. |
[23]
|
徐昊鹏, 朱翀, 弓孟春, 等.中国罕见病研究的现状与未来[J].协和医学杂志, 2018, 9:5-9. |