Pulmonary Capillary Hemangiomatosis (PCH) (A Rare Cause of Pulmonary Hypertension)
(2020). Pulmonary Capillary Hemangiomatosis (PCH) (A Rare Cause of Pulmonary Hypertension). EKB Journal Management System, 4(1), -. doi: 10.21608/cvrepj.2020.351787
. "Pulmonary Capillary Hemangiomatosis (PCH) (A Rare Cause of Pulmonary Hypertension)". EKB Journal Management System, 4, 1, 2020, -. doi: 10.21608/cvrepj.2020.351787
(2020). 'Pulmonary Capillary Hemangiomatosis (PCH) (A Rare Cause of Pulmonary Hypertension)', EKB Journal Management System, 4(1), pp. -. doi: 10.21608/cvrepj.2020.351787
Pulmonary Capillary Hemangiomatosis (PCH) (A Rare Cause of Pulmonary Hypertension). EKB Journal Management System, 2020; 4(1): -. doi: 10.21608/cvrepj.2020.351787

Pulmonary Capillary Hemangiomatosis (PCH) (A Rare Cause of Pulmonary Hypertension)

Cardiovascular Research Prove Journal
Volume 4, Issue 1, 2020  XML PDF (377.76 K)
Document Type: Case Report
DOI: 10.21608/cvrepj.2020.351787
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Abstract
Pulmonary Capillary Hemangiomatosis (PCH)
(A Rare Cause of Pulmonary Hypertension)
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