Pulmonary Hypertension

Pulmonary hypertension groups 2 to 5

Pulmonary arterial hypertension group 1

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Neonatal infection

Pulmonary Hypertension Treated Effectively With Riociguat

Riociguat demonstrated efficacy and safety in pulmonary arterial hypertension and inoperable chronic thromboembolic pulmonary hypertension. Medscape Medical News

Bayer’s Riociguat for Patients with Chronic Thromboembolic Pulmonary Hypertension and Pulmonary ...

Riociguat is the first drug that has consistently demonstrated efficacy in two life-threatening PH indications - chronic thromboembolic pulmonary hypertension (CTEPH) and pulmonary arterial hypertensi...

Miocardin in Pulmonary arterial hypertension

So, what is pulmonary hypertension (PH) is an increase in blood pressure in the pulmonary artery, pulmonary vein, or pulmonary [...]

Disruption of cellular signaling identified in pulmonary arterial hypertension

(Medical Xpress)—Impairment of a key signaling cascade in the pulmonary blood vessels plays an important role in pulmonary arterial hypertension, a Yale study has found. The study appears in the adv...

Older Women May Be at Risk for Pulmonary HTN (CME/CE)

(MedPage Today) -- NATIONAL HARBOR, Md. -- Of patients with systemic hypertension but preserved ejection fraction, those with pulmonary hypertension were more often older and female, a retrospective s...

Pulmonary hypertension deaths and hospitalizations on the rise

(American College of Chest Physicians) New research indicates an increase in the number of US deaths and hospitalizations related to pulmonary hypertension.

Pulmonary Hypertension Pulmonary Hypertension

Pulmonary hypertension (PH), defined as elevated pulmonary artery pressure, is common in the general population and associated with increased mortality. Accordingly, physicians commonly encounter pati...

An endothelial apelin-FGF link mediated by miR-424 and miR-503 is disrupted in pulmonary arterial hypertension

Vascular homeostasis in the lung is disturbed in pulmonary arterial hypertension. Jongmin Kim et al. delineate a new signaling axis controlling endothelial cell proliferation and cytokine production t...

Pulmonary Interstitial Glycogenosis Associated With Pulmonary Hypertension and Hypertrophic Cardiomyopathy.

A neonate with pulmonary interstitial glycogenosis, pulmonary hypertension, and hypertrophic cardiomyopathy is described. The fatal outcome for this patient contrasts with the reported favorable progn...

Schistosomiasis and pulmonary hypertension.

Schistosomiasis is one of the most prevalent chronic infectious diseases in the world. One of its most severe complications, pulmonary hypertension, occurs in up to 5% of patients with hepatosplenic s...

Audit of the aetiology and prevalence of pulmonary hypertension in a tertiary hospital setting.

Appropriate diagnosis and initiation of disease-specific treatment is an important therapeutic goal in idiopathic pulmonary arterial hypertension. We evaluated the prevalence and aetiology of moderate...

Maternal hyperoxygenation test in fetuses undergoing FETO for severe isolated congenital diaphragmatic hernia.

RATIONALE: Pulmonary hypoplasia and hypertension are the main problems in newborns with isolated congenital diaphragmatic hernia (CDH). The outcome can be prenatally predicted by the measurement of co...

Epoprostenol treatment for idiopathic pulmonary arterial hypertension in pregnancy.

Idiopathic pulmonary arterial hypertension is a rare condition associated with significant maternal mortality. We report the management of a 37-year-old multigravida with severe disease using epoprost...