IPH

(redirected from idiopathic pulmonary hemosiderosis)
Also found in: Medical.
AcronymDefinition
IPHI Party Hard
IPHInstitute of Public Health (various locations)
IPHIrrigation and Public Health (India)
IPHIntraparenchymal Hemorrhage (brain)
IPHIntimate Partner Homicide (crime)
IPHIdiopathic Portal Hypertension
IPHIp Header
IPHIowa Pacific Holdings (Chicago, IL)
IPHInpatient Psychiatric Hospital (various locations)
IPHImpressions Per Hour
IPHIdiopathic Pulmonary Hemosiderosis
IPHInternational Association of Paper Historians
IPHInternational Paper Historians (paper watermark database)
IPHInstitute of Population Health (various universities)
IPHItems Per Hour
IPHIpoh, Malaysia - Ipoh (Airport Code)
IPHiPodHacking.com (website)
IPHInstitute of Preparation for the Hereafter
IPHIuphimhan (Vietnamese movie website)
IPHImperial Palace Hotel (Las Vegas, Nevada)
IPHIntraperitoneal Hemorrhage
IPHIndonesia Publishing House
IPHInterval Partitioning Heuristic (computer engineering)
IPHI Play Harder
IPHInternational Partyhouse
References in periodicals archive ?
Idiopathic pulmonary hemosiderosis in adults: review of cases reported in the latest 15 years.
Idiopathic Pulmonary Hemosiderosis in Adults: A Case Report and Review of the Literature.
Long- term clinical course of patients with Idiopathic Pulmonary Hemosiderosis (1979-1994): prolonged survival with low dose corticosteroid therapy.
Recurrence of Idiopathic pulmonary hemosiderosis in a young adult patient after bilateral single lung transplantation.
Idiopathic Pulmonary Hemosiderosis Presenting as a Rare Cause of Iron Deficiency Anemia in a Toddler--A Diagnostic Challenge.
Screening for celiac disease in idiopathic pulmonary hemosiderosis.
Idiopathic pulmonary hemosiderosis (IPH) is a rare disease characterized by heavy lungs with aggregates of hemosiderin-laden macrophages due to recurrent diffuse alveolar hemorrhage in the absence of vasculitis or capillaritis and by eventual interstitial fibrosis (Figure 6).
Treatment of pediatric idiopathic pulmonary hemosiderosis with low-dose cyclophosphamide.
Idiopathic pulmonary hemosiderosis (IPH) is an extremely rare cause of IDA and a potentially lethal disease of unknown etiology.
Cases for which the etiology is undetermined, such as these eight reported from Cleveland, traditionally have been classified as idiopathic pulmonary hemosiderosis (IPH) and account for less than 5% of all cases of pulmonary hemorrhage during infancy.
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