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PAH
(redirected from Pulmonary Arterial Hypertension)

   Also found in: Medical, Wikipedia, Hutchinson 0.03 sec.
AcronymDefinition
PAHPolycyclic Aromatic Hydrocarbon (compound)
PAHPulmonary Arterial Hypertension
PAHPoly (Allylamine Hydrochloride)
PAHPolska Akcja Humanitarna
PAHPhenylalanine Hydroxylase
PAHPolynuclear Aromatic Hydrocarbon (compound)
PAHPolyaromatic Hydrocarbon
PAHP-Aminohippuric Acid
PAHPara-Aminohippuric Acid (used in renal function tests)
PAHPaducah, KY, USA (Airport Code)
PAHPets At Home (UK pet supermarket chain)
PAHProduction Approval Holder
PAHPromoting Awareness in Healthcare
PAHPayload Accommodations Handbook
PAHParents Are Home
PAH4-Aminohippuric Acid (CAS Number 61-78-9)
PAHPrimary Account Holder
PAHPretoria Akademiese Hospitaal (South Africa)
PAHPanzerabwehrhelikopter (German: Anti-Tank Helicopter)
PAHPersonnel Access Hatch
PAHPredictor At Home
PAHDepartment of Pathology at Pennsylvania Hospital


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? References in periodicals archive
TSE: 4503) today announced that Toray has obtained marketing approval for its oral PGI2 derivative prolonged release, Careload(R) LA Tablets 60mu/g (generic name: beraprost sodium), to be indicated for pulmonary arterial hypertension (PAH) on October 19,2007.
Abstract: Pulmonary arterial hypertension (PAH), a rare disease involving the pulmonary vascular circuit, is defined as an elevation in pulmonary arterial pressures and is characterized by symptoms of dyspnea, chest pain, and syncope.
Recently, 2 articles from 1 group suggested that HHV-8 has a role in the pathogenesis of idiopathic pulmonary arterial hypertension (
 
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