1. Trang chủ
  2. » Kỹ Năng Mềm

Andersons pediatric cardiology 1589

3 3 0

Đang tải... (xem toàn văn)

THÔNG TIN TÀI LIỆU

1982;104(1):115–135 208 Gott VL, Cameron DE, Alejo DE, et al Aortic root replacement in 271 marfan patients: a 24 year experience Ann Thorac Surg 2002;73(2):438–443 209 Januzzi JL, Marayati F, Mehta RH, et al Comparison of aortic dissection in patients with and without Marfan's syndrome (results from the internation registry of aortic dissection) Am J Cardiol 2004;94(3):400–402 210 Elefteriades JA Natural history of thoracic aortic aneurysms: indications for surgery, and surgical versus nonsurgical risks Ann Thorac Surg 2002;74(5):S1877–S1880 211 Hiratzka LF, Bakris GL, Beckman JA, et al 2010 ACCF/AHA/AATS/ASA/SCA/SCAI/SIR/STS/SVM guidelines for the diagnosis and management of patients with thoracic aortic disease Circulation 2010;121:e266–e369 212 Kallenbach K, Baraki H, Khaladi NKamiya H, et al Aortic valve-sparing operation in MArfan syndrome: what do we know after a decade? Ann Thorac Surg 2007;83(2):S785–S790 213 Settepani F, Szeto WY, Pacini D, et al Reimplantation valve-sparing aortic root replacement in Marfan Syndrome using the valsalva conduit: an intercontinental multicenter study Ann Thorac Surg 2007;83(2):S769–S773 214 Lacro RV, Dietz HC, Sleeper AT, et al Atenolol versus losartan in children and young adults with Marfan's syndrome N Eng J Med 2014;371:2061–2071 215 Geva T, Sanders SP, Diogenes MS, Rockenmacher S, Van Praagh R Twodimensional and doppler echocardiographic and pathologic characteristics of the infantile Marfan Syndrome Am J Cardiol 1990;65:1230–1237 216 Morse RP, Rockenmacher S, Pyeritz RE, et al Diagnosis and management of infantile Marfan Syndrome Pediatrics 1990;86(6):888–895 217 El-Habbal MH Cardiovascular manifestations of Marfan's syndrome in the young Am Heart J 1992;123:752–757 218 Loeys BL, Chen J, Neptune ER, et al A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development cause by mutations in TGFBR1 or TGFBR2 Nat Genet 2005;37(3):275–281 219 Williams JA, Loeys BL, Nwakanma LU, et al Early surgical experience with Loeys-dietz: a new syndrome of aggressive thoracic aortic aneurysm disease Ann Thorac Surg 2007;83(2):S757–S763 220 Hiratzka LF, Bakris GL, Beckman JA, et al 2010 ACCF/AHA/AATS/ASA/SCA/SCAI/SIR/STS/SVM guidelines for the diagnosis and management of patients with thoracic aortic disease Circulation 2010;121:e266–e369 221 Bellamy MF, McDowell IF Putative mechanisms for vascular damage by homocysteine J Inherit Metab Dis 1997;20:307–315 222 Dudley RW, Danialou G, Govindaraju K, et al Sarcolemmal damage in dystrophin deficiency is modulated by syngeristic interactions between mechanical and oxidative/nitrosative stresses Am J Pathol 2006;168(4):1276–1287 223 Gloss D, Moxley RT, Ashwal S, Oskoui M Practice guideline update summary: corticosteroid treatment of duchenne muscular dystrophy: report of the guideline development subcommittee of the American academy of neurology Neurology 2016;86(5):465–472 224 Gulati S, Saxena A, Kumar V, Kalra V Duchenne muscular dystrophy: prevalence and patterns of cardiac involvement Indian J Pediatr 2005;72(5):389–393 225 Kirchmann C, Kececioglu D, Korinthenberg R, Dittrich S Echocardiographic and electrocardiographic findings of cardiomyopathy in duchenne and Becker-kiener muscular ... Morse RP, Rockenmacher S, Pyeritz RE, et al Diagnosis and management of infantile Marfan Syndrome Pediatrics 1990;86(6):888–895 217 El-Habbal MH Cardiovascular manifestations of Marfan's syndrome in the young

Ngày đăng: 22/10/2022, 13:04

Xem thêm: