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Pulmonary Arterial Hypertension: what is it?
How is Pulmonary Arterial Hypertension diagnosed?
What can be done to treat Pulmonary Arterial Hypertension?
Glossary
Further information and links
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A
Actelion Affiliates
Anticoagulants
Associated pulmonary arterial hypertension (APAH)
Autoantibody
C
Calcium channel blockers
Classifying severity of Pulmonary Arterial Hypertension
Collagen
Congenital heart disease
Connective tissue disease (CTD)
CT scan (Computerised Tomography)
Cyanosis
D
Diffuse cutaneous systemic sclerosis (dcSSc)
Diuretics
Dyspnoea
E
Echocardiography or Doppler echocardiogram
EEisenmenger’s Syndrome / Physiology
Electrocardiogram (ECG)
Endothelin (ET)
Endothelin receptor antagonist (ERA)
Endothelin receptors
Endothelium
Extracellular matrix
F
Familial pulmonary arterial hypertension (FPAH)
Fibroblasts
Fibrosis
Further information and links
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Glossary
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Home Page
How is Pulmonary Arterial Hypertension classified?
How is Pulmonary Arterial Hypertension diagnosed?
Human immunodeficiency virus (HIV)
Hypertrophy
I
I am a Patient
Idiopathic pulmonary arterial hypertension (IPAH)
Inflammation
Interstitial lung disease
Is Pulmonary Arterial Hypertension very common?
Ischaemia
L
Limited cutaneous systemic sclerosis (LcSSc)
N
New York Heart Association (NYHA)
Nitric oxide (NO)
P
Patient Associations
Patient site map
Portal hypertension
Primary pulmonary hypertension (PPH)
Prostacyclin
Prostanoids
Pulmonary arterial hypertension (PAH)
Pulmonary Arterial Hypertension: what is it?
Pulmonary artery
Pulmonary fibrosis
R
Remodelling
Right heart catheterisation
RRaynaud’s phenomenon
S
Scleroderma or Systemic Sclerosis
Sleep Apnoea
Syncope (fainting)
Systemic lupus erythematosus (SLE) or Lupus
T
Telangiectases
V
Vascular remodelling
Vasculopathy
Vasoconstriction
Vasodilation
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What are common symptoms of Pulmonary Arterial Hypertension?
What can be done to treat Pulmonary Arterial Hypertension?
What causes Pulmonary Arterial Hypertension?
WHO Functional Class
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