SummaryBackgroundThe pathogenesis of idiopathic pulmonary arterial hypertension (IPAH) is unknown, and the syndrome of IPAH remains a diagnostic and therapeutic challenge. The present study investigated the disease-specific proteins that aid in the diagnosis of IPAH and thus to study their role in the disease process.MethodsA comparative proteomic analysis was used for clinical screening of serum proteins in 10 patients with IPAH and compared with 10 normal subjects. Furthermore, enzyme linked immunosorbent assay (ELISA) was performed for comparison with serum proteins between individual IPAH patients and controls.ResultsNine proteins and their isoforms, including leucine-rich α-2-glycoprotein (LRG), haptoglobin precursor, albumin isoform 2...
Idiopathic pulmonary fibrosis (IPF) is a lung parenchymal disease of unknown cause usually occurring...
Pulmonary arterial hypertension (PAH) is a severe disease usually diagnosed by echocardiography and ...
Idiopathic pulmonary arterial hypertension (IPAH) is a life-threatening cardiopulmonary disease lack...
SummaryBackgroundThe pathogenesis of idiopathic pulmonary arterial hypertension (IPAH) is unknown, a...
BACKGROUND: Idiopathic and heritable pulmonary arterial hypertension form a rare but molecularly het...
Idiopathic pulmonary arterial hypertension (IPAH) is a rare but fatal disease diagnosed by right hea...
Idiopathic pulmonary arterial hypertension (IPAH) is a rare but fatal disease diagnosed by right hea...
Background: Chronic anticoagulation is a standard of care in idiopathic pulmonary arterial hypertens...
Idiopathic pulmonary arterial hypertension (IPAH) is a progressive disease characterised by increase...
Aim: The aim of the present study was to identify the possible genotypic association of 3\u2032UTR H...
BACKGROUND: Chronic anticoagulation is a standard of care in idiopathic pulmonary arterial hypertens...
Rationale: Autoimmunity is believed to play a role in idiopathic pulmonary arterial hypertension (IP...
We previously reported that osteoprotegerin (OPG) is regulated by pathways associated with pulmonary...
Pulmonary arterial hypertension (PAH) is a rare but fatal cardiovascular disorder with high morbidit...
Rationale The blood is a rich source of potential biomarkers for the diagnosis of idiopathic and her...
Idiopathic pulmonary fibrosis (IPF) is a lung parenchymal disease of unknown cause usually occurring...
Pulmonary arterial hypertension (PAH) is a severe disease usually diagnosed by echocardiography and ...
Idiopathic pulmonary arterial hypertension (IPAH) is a life-threatening cardiopulmonary disease lack...
SummaryBackgroundThe pathogenesis of idiopathic pulmonary arterial hypertension (IPAH) is unknown, a...
BACKGROUND: Idiopathic and heritable pulmonary arterial hypertension form a rare but molecularly het...
Idiopathic pulmonary arterial hypertension (IPAH) is a rare but fatal disease diagnosed by right hea...
Idiopathic pulmonary arterial hypertension (IPAH) is a rare but fatal disease diagnosed by right hea...
Background: Chronic anticoagulation is a standard of care in idiopathic pulmonary arterial hypertens...
Idiopathic pulmonary arterial hypertension (IPAH) is a progressive disease characterised by increase...
Aim: The aim of the present study was to identify the possible genotypic association of 3\u2032UTR H...
BACKGROUND: Chronic anticoagulation is a standard of care in idiopathic pulmonary arterial hypertens...
Rationale: Autoimmunity is believed to play a role in idiopathic pulmonary arterial hypertension (IP...
We previously reported that osteoprotegerin (OPG) is regulated by pathways associated with pulmonary...
Pulmonary arterial hypertension (PAH) is a rare but fatal cardiovascular disorder with high morbidit...
Rationale The blood is a rich source of potential biomarkers for the diagnosis of idiopathic and her...
Idiopathic pulmonary fibrosis (IPF) is a lung parenchymal disease of unknown cause usually occurring...
Pulmonary arterial hypertension (PAH) is a severe disease usually diagnosed by echocardiography and ...
Idiopathic pulmonary arterial hypertension (IPAH) is a life-threatening cardiopulmonary disease lack...