Tài liệu tham khảo |
Loại |
Chi tiết |
9. Banikazemi M., Bultas J., Waldek S.. et al. (2007), “Agalsidase-beta therapy for advanced Fabry disease: a randomized trial”, Ann Intern Med, 146, pp. 77-86 |
Sách, tạp chí |
Tiêu đề: |
Agalsidase-beta therapy for advanced Fabry disease: a randomized trial”, "Ann InternMed |
Tác giả: |
Banikazemi M., Bultas J., Waldek S.. et al |
Năm: |
2007 |
|
10. Baumgartner H., Hung J., Bermejo J., et al. (2009). “Echocardiography Assessment of Valve Stenosis: EAE/ASE Recommendations for Clinical Practice”, J Am Soc Echocardiogr, 22(1), pp. 19-20 |
Sách, tạp chí |
Tiêu đề: |
Echocardiography Assessment of Valve Stenosis: EAE/ASE Recommendations for Clinical Practice”, "J Am Soc Echocardiogr |
Tác giả: |
Baumgartner H., Hung J., Bermejo J., et al |
Năm: |
2009 |
|
11. Bennett S.T., Barnes C., Cox A., et al. (2005), “Toward the 1,000 dollars human genome”, Pharmacogenomics, 6(4), pp. 373-82 |
Sách, tạp chí |
Tiêu đề: |
Toward the 1,000 dollars human genome”, "Pharmacogenomics |
Tác giả: |
Bennett S.T., Barnes C., Cox A., et al |
Năm: |
2005 |
|
12. Betocchi S., Cannon R. O. III, Watson R. M., et al. (1985), “Effects of sublingual nifedipine on hemodynamics and systolic and diastolic function in patients with hypertrophic cardiomyopathy”,Circulation, 72, pp. 1001–1007 |
Sách, tạp chí |
Tiêu đề: |
Effects of sublingual nifedipine on hemodynamics and systolic and diastolic function in patients with hypertrophic cardiomyopathy”, "Circulation |
Tác giả: |
Betocchi S., Cannon R. O. III, Watson R. M., et al |
Năm: |
1985 |
|
13. Biesecker L.G., Green R.C. et al. (2014), “Diagnostic clinical genome and exome sequencing”, N Engl J Med, 370(25), pp. 2418-25 |
Sách, tạp chí |
Tiêu đề: |
Diagnostic clinical genome and exome sequencing”, "N Engl J Med |
Tác giả: |
Biesecker L.G., Green R.C. et al |
Năm: |
2014 |
|
14. Blair E., Redwood C., Ashrafian H., et al. (2001), “Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis”, Hum Mol Genet, 10, pp. 1215-1220 |
Sách, tạp chí |
Tiêu đề: |
Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis”, "Hum Mol Genet |
Tác giả: |
Blair E., Redwood C., Ashrafian H., et al |
Năm: |
2001 |
|
15. Bollen A. E, Schuldt M., Harakalova M., (2017), “Genotype-Specific Pathogenic Effects in Human Dilated Cardiomyopathy”, The Journal of Physiology, 595(14), pp. 4677–4693 |
Sách, tạp chí |
Tiêu đề: |
Genotype-SpecificPathogenic Effects in Human Dilated Cardiomyopathy”, "The Journal of Physiology |
Tác giả: |
Bollen A. E, Schuldt M., Harakalova M |
Năm: |
2017 |
|
17. Bonow R. O., Mann D. L., Zipes D. P., et al. (2012), “Hypertrophic cardiomyopathy”, Braunwald's Heart Disease. A Textbook of Cardiovascular Medicine, 9th ed, Saunders Elsevier, Philadelphia, chapter 69, pp. 1582-1593 |
Sách, tạp chí |
Tiêu đề: |
Hypertrophic cardiomyopathy”, "Braunwald's Heart Disease. A Textbook of Cardiovascular Medicine |
Tác giả: |
Bonow R. O., Mann D. L., Zipes D. P., et al |
Năm: |
2012 |
|
18. Bos J. M., Towbin A. T., Ackerman M. J. (2009), “Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy”, J. Am. Coll. Cardiol, 54, pp. 201- 211 |
Sách, tạp chí |
Tiêu đề: |
Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy”, "J. Am. Coll. Cardiol |
Tác giả: |
Bos J. M., Towbin A. T., Ackerman M. J |
Năm: |
2009 |
|
19. Bottillo I., D’Angelantonio D., Caputo V., et al. (2016), “Molecular analysis of sarcomeric and non-sarcomeric genes in patients with hypertrophic cardiomyopathy”, Gene, 577(2), pp. 227-235 |
Sách, tạp chí |
Tiêu đề: |
Molecular analysis of sarcomeric and non-sarcomeric genes in patients with hypertrophic cardiomyopathy”, "Gene |
Tác giả: |
Bottillo I., D’Angelantonio D., Caputo V., et al |
Năm: |
2016 |
|
20. Braunwald E., Lambrew C. D., Rockoff S. D., et al. (1964),” Idiopathic hypertrophic subaortic stenosis: A description of the disease based upon an analysis of 64 patients”. Circulation, 30, pp. 3-217 |
Sách, tạp chí |
Tiêu đề: |
Circulation |
Tác giả: |
Braunwald E., Lambrew C. D., Rockoff S. D., et al |
Năm: |
1964 |
|
21. Braunwald E., Lambrew C. T., Rockoff S. D., Ross J. Jr., et al. (1964), “Idiopathic hypertrophic subaortic stenosis: a description of the disease based upon an analysis of 64 patients”, Circulation, 30, SUPPL 4, pp. 3-119 |
Sách, tạp chí |
Tiêu đề: |
Idiopathic hypertrophic subaortic stenosis: a description of the disease based upon an analysis of 64 patients”, "Circulation |
Tác giả: |
Braunwald E., Lambrew C. T., Rockoff S. D., Ross J. Jr., et al |
Năm: |
1964 |
|
22. Cannan C. R., Reeder G. S., Bailey K. R., et al. (1995), “Natural history of hypertrophic cardiomyopathy. A population-based study, 1976 through 1990”, Circulation, 92, pp. 2488-2495 |
Sách, tạp chí |
Tiêu đề: |
Natural history of hypertrophic cardiomyopathy. A population-based study, 1976 through 1990”, "Circulation |
Tác giả: |
Cannan C. R., Reeder G. S., Bailey K. R., et al |
Năm: |
1995 |
|
23. Cannon R. O. III, Rosing D. R., Maron B. J., et al. (1985), “Myocardial ischemia in patients with hypertrophic cardiomyopathy:contribution of inadequate vasodilator reserve and elevated left ventricular filling pressures”, Circulation, 71, pp. 234-243 |
Sách, tạp chí |
Tiêu đề: |
Myocardial ischemia in patients with hypertrophic cardiomyopathy: contribution of inadequate vasodilator reserve and elevated left ventricular filling pressures |
Tác giả: |
Cannon R. O. III, Rosing D. R., Maron B. J., et al |
Năm: |
1985 |
|
25. Carniel E., Taylor M. R., Sinagra G., Di Lenarda A. et al. (2005), “Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy”, Circulation, 112(1), pp. 54–59 |
Sách, tạp chí |
Tiêu đề: |
Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy”, "Circulation |
Tác giả: |
Carniel E., Taylor M. R., Sinagra G., Di Lenarda A. et al |
Năm: |
2005 |
|
26. Carrier L., Bonne G., Bọhrend E., et al. (1997), “Organization and sequence of human cardiac myosin binding protein C gene (MYBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy”. Circ Res, 80, pp. 427–434 |
Sách, tạp chí |
Tiêu đề: |
Organization and sequence of human cardiac myosin binding protein C gene ("MYBPC3") and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy”. "Circ Res |
Tác giả: |
Carrier L., Bonne G., Bọhrend E., et al |
Năm: |
1997 |
|
27. Chiou K. R., Chu C. T., Charng M. J. (2015), “Detection of mutations in symptomatic patients with hypertrophic cardiomyopathy inTaiwan”, J Cardiol, 65, pp. 250 – 256 |
Sách, tạp chí |
Tiêu đề: |
Detection of mutations in symptomatic patients with hypertrophic cardiomyopathy in Taiwan”, "J Cardiol |
Tác giả: |
Chiou K. R., Chu C. T., Charng M. J |
Năm: |
2015 |
|
28. Christiaans I., Birnie E., Bonsel G. J., et al. (2011), “Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophiccardiomyopathy mutation carriers: determining the bestcardiological screening strategy”, European Heart Journal, 32, pp.1161–1170 |
Sách, tạp chí |
Tiêu đề: |
Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy”, "European Heart Journal |
Tác giả: |
Christiaans I., Birnie E., Bonsel G. J., et al |
Năm: |
2011 |
|
29. Consevage M. W., Salada G. C., Baylen B. G., (1994), “A New Missense Mutation, Arg719Gln, in the Beta-Cardiac Heavy Chain Myosin Gene of Patients with Familial Hypertrophic Cardiomyopathy”, Human Molecular Genetics, 3(6), pp. 1025–1026 |
Sách, tạp chí |
Tiêu đề: |
A NewMissense Mutation, Arg719Gln, in the Beta-Cardiac Heavy ChainMyosin Gene of Patients with Familial HypertrophicCardiomyopathy”, "Human Molecular Genetics |
Tác giả: |
Consevage M. W., Salada G. C., Baylen B. G |
Năm: |
1994 |
|
31. Davies J. P., Winchester B. G., Malcolm S., (1993), “Mutation Analysis in Patients with the Typical Form of Anderson-Fabry Disease”, Human Molecular Genetics, 2(7), pp. 1051–1053 |
Sách, tạp chí |
Tiêu đề: |
Mutation Analysis in Patients with the Typical Form of Anderson-Fabry Disease”, "Human Molecular Genetics |
Tác giả: |
Davies J. P., Winchester B. G., Malcolm S |
Năm: |
1993 |
|