| 1. |
Pantazis A, Elliott PM. Left ventricular noncompaction[J]. Curr Opin Cardiol, 2009, 24(3):209-213.
|
| 2. |
Maron BJ, Towbin JA. Contemporary definitions and classification of the cardiomyopathies:an American Heart Association Scientific Statement from the Council on Clinical Cardiology, Heart Failure and Transplantation Committee; Quality of Care and Outcomes Research and Functional Genomics and Translational Biology Interdisciplinary Working Groups; and Council on Epidemiology and Prevention[J]. Circulation, 2006, 113(14):1807-1816.
|
| 3. |
Elliott P, Andersson B, 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(2):270-276.
|
| 4. |
Bartram U, Bauer J, Schranz D. Primary noncompaction of the ventricular myocardium from the morphogenetic standpoint[J]. Pediatr Cardiol, 2007, 28(5):325-332.
|
| 5. |
Burke A, Mont E, Kutys R, et al. Left ventricular noncompaction:a pathological study of 14 cases[J]. Hum Pathol, 2005, 36(4):403-411.
|
| 6. |
Jenni R, Oechslin E, Schneider J, et al. Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction:a step towards classification as a distinct cardiomyopathy[J]. Heart, 2001, 86(6):666-671.
|
| 7. |
Stöllberger C, Kopsa W, Tscherney R, et al. Diagnosing left ventricular noncompaction by echocardiography and cardiac magnetic resonance imaging and its dependency on neuromuscular disorders[J]. Clin Cardiol, 2008, 31(8):383-387.
|
| 8. |
Bione S, D'adamo P, Maestrini E, et al. A novel X-linked gene, G4.5. is responsible for Barth syndrome[J]. Nat Genet, 1996, 12(4):385-389.
|
| 9. |
Bleyl SB, Mumford BR, Brown-Harrison MC, et al. Xq28-linked noncompaction of the left ventricular myocardium:prenatal diagnosis and pathologic analysis of affected individuals[J]. Am J Med Genet, 1997, 72(3):257-265.
|
| 10. |
Phoon CK, Acehan D, Schlame M, et al. Tafazzin knockdown in mice leads to a developmental cardiomyopathy with early diastolic dysfunction preceding myocardial noncompaction[J]. J Am Heart Assoc, 2012, 1(2):jah3-e000455.
|
| 11. |
Ichida F, Tsubata S, Bowles KR, et al. Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome[J]. Circulation, 2001, 103(9):1256-1263.
|
| 12. |
Vatta M, Mohapatra B, Jimenez S, et al. Mutations in cypher/ZASP in patients with dilated cardiomyopathy and left ventricular noncompaction[J]. J Am Coll Cardiol, 2003, 42(11):2014-2027.
|
| 13. |
Xi Y, Ai T, De Lange E, et al. Loss of function of hNav1.5 by a ZASP1 mutation associated with intraventricular conduction disturbances in left ventricular noncompaction[J]. Circ Arrhythm Electrophysiol, 2012, 5(5):1017-1026.
|
| 14. |
Probst S, Oechslin E, Schuler P, et al. Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype[J]. Circ Cardiovasc Genet, 2011, 4(4):367-374.
|
| 15. |
Klaassen S, Probst S, Oechslin E, et al. Mutations in sarcomere protein genes in left ventricular noncompaction[J]. Circulation, 2008, 117(22):2893-2901.
|
| 16. |
Monserrat L, Hermida-Prieto M, Fernandez X, et al. Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular noncompaction, and septal defects[J]. Eur Heart J, 2007, 28(16):1953-1961.
|
| 17. |
Tang S, Batra A, Zhang Y, et al. Left ventricular noncompaction is associated with mutations in the mitochondrial genome[J]. Mitochondrion, 2010, 10(4):350-357.
|
| 18. |
Chin TK, Perloff JK, Williams RG, et al. Isolated noncompaction of left ventricular myocardium. A study of eight cases[J]. Circulation, 1990, 82(2):507-513.
|
| 19. |
Stöllberger C, Finsterer J, Blazek G. Left ventricular hypertrabeculation/noncompaction and association with additional cardiac abnormalities and neuromuscular disorders[J]. Am J Cardiol, 2002, 90(8):899-902.
|
| 20. |
Kohli SK, Pantazis AA, Shah JS, et al. Diagnosis of left-ventricular non-compaction in patients with left-ventricular systolic dysfunction:time for a reappraisal of diagnostic criteria?[J]. Eur Heart J, 2008, 29(1):89-95.
|
| 21. |
Sen-Chowdhry J, Mckenna WJ. Left ventricular noncompaction and cardiomyopathy:cause, contributor, or epiphenomenon[J]. Curr Opin Cardiol, 2008, 23(3):171-175.
|
| 22. |
Thuny F, Jacquier A, Jop B, et al. Assessment of left ventricular non-compaction in adults:side-by-side comparison of cardiac magnetic resonance imaging with echocardiography[J]. Arch Cardiovasc Dis, 2010, 103(3):150-159.
|
| 23. |
Petersen SE, Selvanayagam JB, Wiesmann F, et al. Left ventricular non-compaction:insights from cardiovascular magnetic resonance imaging[J]. J Am Coll Cardiol, 2005, 46(1):101-105.
|
| 24. |
Jacquier A, Thuny F, Jop B, et al. Measurement of trabeculated left ventricular mass using cardiac magnetic resonance imaging in the diagnosis of left ventricular non-compaction[J]. Eur Heart J, 2010, 31(9):1098-1104.
|
| 25. |
Dodd JD, Holmvang G, Hoffmann U, et al. Quantification of left ventricular noncompaction and trabecular delayed hyperenhancement with cardiac MRI:correlation with clinical severity[J]. AJR, 2007, 189(4):974-980.
|
| 26. |
Oechslin EN, Attenhofer Jost CH, Rojas JR, et al. Long-term follow-up of 34 adults with isolated left ventricular noncompaction:a distinct cardiomyopathy with poor prognosis[J]. J Am Coll Cardiol, 2000, 36(2):493-500.
|
| 27. |
Murphy RT, Thaman R, Blanes JG, et al. Natural history and familial characteristics of isolated left ventricular non-compaction[J]. Eur Heart J, 2005, 26(2):187-192.
|
| 28. |
Ichida F, Hamamichi Y, Miyawaki T, et al. Clinical features of isolated noncompaction of the ventricular myocardium:long-term clinical course, hemodynamic properties, and genetic background[J]. J Am Coll Cardiol, 1999, 34(1):233-240.
|
1/5
WeChat