IPAH

(redirected from Idiopathic Pulmonary Arterial Hypertension)
AcronymDefinition
IPAHIdiopathic Pulmonary Arterial Hypertension
IPAHInternet Protocol Authentication Header
IPAHIdiopathische Pulmonal Arterielle Hypertonie (German: Idiopathic Pulmonary Arterial Hypertension; cardiopulmonary medicine)
IPAHInvasion Plasmid Antigen H Gene
References in periodicals archive ?
Predictors of health-related quality of life in patients with idiopathic pulmonary arterial hypertension.
Idiopathic pulmonary arterial hypertension remains mostly a clinical diagnosis because patients with this condition do not typically undergo biopsy.
Reduced number and activity of circulating endothelial progenitor cells in patients with idiopathic pulmonary arterial hypertension.
Human herpesvirus 8 (HHV-8) seroprevalence among candidate patients for lung transplantation Diagnosis Patients Female sex (%) Patients with pulmonary hypertension Idiopathic pulmonary arterial hypertension 16 14 (87.
Clinical efficacy and survival with first-line inhaled iloprost therapy in patients with idiopathic pulmonary arterial hypertension.
Pulmonary arterial hypertension (PAH) is now classified as either idiopathic pulmonary arterial hypertension (IPAH), formally known as primary pulmonary hypertension, or familial pulmonary arterial hypertension (FPAH).
Idiopathic pulmonary arterial hypertension (PAH) is included in Group 1 of PAH classification, while pulmonary veno- occlusive disease (PVOD), pulmonary capillary hemangiomatosis (PCH), portopulmonary hypertension (PoPH) and HIV-associated PAH constitute the subgroups of Group I PAH disorders.
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