Pulmonary Hypertension in Pulmonary Langerhans Cell Histiocytosis: prevalence and the role of Cardiopulmonary Exercise Testing and echocardiogram in predicting it

G. Itamaro Heiden (São Paulo, Brazil), J. Barbosa Sobral (São Paulo, Brazil), J. Alves Jr (São Paulo, Brazil), J. Salge (São Paulo, Brazil), A. Albuquerque (São Paulo, Brazil), C. Fernandes (São Paulo, Brazil), R. Kairalla (São Paulo, Brazil), C. Ribeiro Carvalho (São Paulo, Brazil), R. Souza (São Paulo, Brazil), B. Guedes Baldi (São Paulo, Brazil)

Source: International Congress 2019 – Innovative approaches for management and treatment of rare diffuse parenchymal lung diseases
Disease area: Interstitial lung diseases, Pulmonary vascular diseases

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G. Itamaro Heiden (São Paulo, Brazil), J. Barbosa Sobral (São Paulo, Brazil), J. Alves Jr (São Paulo, Brazil), J. Salge (São Paulo, Brazil), A. Albuquerque (São Paulo, Brazil), C. Fernandes (São Paulo, Brazil), R. Kairalla (São Paulo, Brazil), C. Ribeiro Carvalho (São Paulo, Brazil), R. Souza (São Paulo, Brazil), B. Guedes Baldi (São Paulo, Brazil). Pulmonary Hypertension in Pulmonary Langerhans Cell Histiocytosis: prevalence and the role of Cardiopulmonary Exercise Testing and echocardiogram in predicting it. 3684

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