Long-term outcome of bosentan treatment in idiopathic pulmonary arterial hypertension and pulmonary arterial hypertension associated with the scleroderma spectrum of diseases. Journal of Heart and Lung Transplantation 24(10): 1626-1631, 2005
Pulmonary arterial capacitance in children with idiopathic pulmonary arterial hypertension and pulmonary arterial hypertension associated with congenital heart disease: relation to pulmonary vascular resistance, exercise capacity, and survival. American Heart Journal 162(3): 562-568, 2011
Long-term survival in idiopathic pulmonary arterial hypertension associated with massive pulmonary artery dilation. Canadian Respiratory Journal 18(3): E50-E51, 2012
Idiopathic pulmonary arterial hypertension in Asians: a long-term study on clinical outcomes. Chest 147(4): E160-E163, 2015
Long-term outcomes of domiciliary intravenous iloprost in idiopathic and connective tissue disease-associated pulmonary arterial hypertension. Respirology (): -, 2016
Potts shunt in children with idiopathic pulmonary arterial hypertension: long-term results. Annals of Thoracic Surgery 94(3): 817-824, 2012
Long-term patient survival with idiopathic/heritable pulmonary arterial hypertension treated at a single center in Japan. Life Sciences 118(2): 414-419, 2015
Long term combination treatment for severe idiopathic pulmonary arterial hypertension. World Journal of Cardiology 2(3): 68-70, 2010
Plasma proteomics of differential outcome to long-term therapy in children with idiopathic pulmonary arterial hypertension. Proteomics. Clinical Applications 6(5-6): 257-267, 2012
Survival in childhood pulmonary arterial hypertension: insights from the registry to evaluate early and long-term pulmonary arterial hypertension disease management. Circulation 125(1): 113-122, 2012
Predicting survival in pulmonary arterial hypertension: insights from the Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL). Circulation 122(2): 164-172, 2010
The long-term response to treatment with calcium channel blockers in a patient with idiopathic pulmonary arterial hypertension. Bratislavske Lekarske Listy 114(5): 283-286, 2014
Validation of the Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL) pulmonary hypertension prediction model in a unique population and utility in the prediction of long-term survival. Journal of Heart and Lung Transplantation 31(11): 1165-1170, 2013
Long-term outcomes in children with pulmonary arterial hypertension treated with bosentan in real-world clinical settings. American Journal of Cardiology 106(9): 1332-1338, 2010
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