可能因为您的浏览器不支持样式,您可以更新您的浏览器到最新版本,以获取对此功能的支持,访问下面的网站,获取关于浏览器的信息:
[1]GinSing W.Pulmonary arterial hypertension:a multidisciplinary approach to care[J].Nursing Stand,2010,24(38):40-47.
[2]Marelli AJ,Therrien J,Mackie AS,et al.Planning the specialized care of adult congenital heart disease patients: from numbers to guidelines;an epidemiologic approach[J].Am Heart J,2009,157(1):1-8.
[3]Harrison JL,Silversides CK,Oechslin EN,et al. Health care needs of adults with congenital heart disease,Study of the patient perspective[J]. J Cardiovasc Nurs,2011,26(6):497-503.
[4]Hoendermis ES.Pulmonary arterial hypertension: an update[J].Neth Heart J,2011,19(12):514-522.
[5]Natarajan R.Recent trend in pulmonary arterial hypertention[J].Lung India,2011,28(1):39-48.
[6]Park MH.Advances in diagnosis and treatment in patients with pulmonary arterial hypertension[J].Catheter Cardiovasc Interv,2008,71(2):205-213.
[7]Teixeira FM,Coelho RM,Proena C,et al.Quality of Life experienced by adolescents and young adults with congenital heart disease[J].Pediatr Cardiol, 2011,32(8):1132-1138.
[8]McCollister DH,Beutz M,McLaughlin V,et al.Depressive symptoms in pulmonary arterial hypertension:prevalence and association with functional status[J].Psychosomatics, 2010,51(4):339-339.
[9]Silva AM,Vaz C,Areias ME,et al.Quality of life of patients with congenital heart diseases[J].Cardiol Young,2011,21(6):670-676.
[10]Galiè N,Hoeper MM,Humbert M,et al.Guidelines for the diagnosis and treatment of pulmonary hypertension:The task force for the diagnosis and treatment of pulmonary hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS), endorsed by the International Society of Heart and Lung Transplantation(ISHLT)[J].Eur Heart J,2009,30(2):2493-2537.
[11]吴险峰,程应樟.先天性心脏病并肺动脉高压研究新进展[J].岭南心血管病杂志,2009,15(6):485-488.
[12]丁仲如,秦永文.先天性心脏病合并肺动脉高压分级及性质的评估[J].介入放射学杂志,2008,17(7):523-526.
[13]钱红波,杨小龙.先天性心脏病合并肺动脉高压的诊疗进展[J].华北煤炭医学院学报,2011,13(2):176-178.
[14]Beghetti M,Tissot C.The right heart and pulmonary circulation(X):Pulmonary hypertension in congenital shunts[J].Rev Esp Cardiol,2010,63(10):1179-1193.
[15]Schuuring MJ,van Riel AC,Bouma BJ,et al.Recent progress in treatment of pulmonary arterial hypertension due to congenital heart disease[J].Neth Heart J,2011,19(12):495-497.
[16]Schuuring MJ,Boekholdt SM,Windhausen A,et al.Advanced therapy for pulmonary arterial hypertension due to congenital heart disease: a clinical perspective in a new therapeutic era[J].Neth Heart J,2011,19(12):509-513.
[17]Zeng WJ,Lu XL,Xiong CM,et al.The efficacy and safety of sildenafil in patients with pulmonary arterial hypertension associated with the different types of congenital heart disease[J].Clin Cardiol,2011,34(8):513-518.
[18]Madden BP.Pulmonary hypertension and pregnancy[J].Int J Obstet Anesth,2009,18(2):156-164.
[19]Badesch DB,Champion HC,Sanchez MA,et al.Diagnosis and assessment of pulmonary arterial hypertension[J].J Am Coll Cardiol,2009,54(1 Suppl):S55-S66.
[20]Diller GP,Gatzoulis MA.Pulmonary vascular disease in adults with congenital heart disease[J].Circulation,2007,115(8):1039-1050.
[21]Van De Bruaene A,Delcroix M,Pasquet A,et al.Iron deficiency is associated with adverse outcome in Eisenmenger patients[J].European Heart Journal,2011,32(22):2790-2799.
[22]邬晓臣,张近宝,欧阳辉,等.提高先天性心脏病并发肺动脉高压外科治疗效果的综合方案[J].心脏杂志,2012,24(3):381-384.