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ECDEducation and Curriculum Development (various locations)
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ECDTotal Commercial Energy Demand (Carolina Environmental Program)
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References in periodicals archive ?
Consensus guidelines for the diagnosis and clinical management of Erdheim-Chester disease. Blood 2014;124:483-492.
Given the morphologic appearance of Mikulicz cells, one must consider various histiocytic lesions, such as Rosai-Dorfman disease and Erdheim-Chester disease. Rosai-Dorfmann disease presents classically with massive, painless cervical lymphadenopathy with extranodal disease most commonly affecting the skin and central nervous system.
Erdheim-Chester disease (ECD) is a rare form of a non-langerhans histiocytic disorder.
M2 PHARMA-November 8, 2017-FDA Approves Zelboraf for Erdheim-Chester Disease with BRAF V600 Mutation
M2 EQUITYBITES-November 7, 2017-Hoffman-LaRoche wins US FDA approval for Zelboraf to treat Erdheim-Chester Disease (ECD)
Erdheim-Chester disease (ECD) is one of the non-Langerhans cell histiocytosis.
Shoenfeld, "Erdheim-Chester disease: a comprehensive review of the literature," Orphanet Journal of Rare Diseases, vol.
Boyd et al., "The clinical spectrum of Erdheim-Chester disease: an observational cohort study," Blood Advances, vol.
The Erdheim-Chester Disease (ECD) (also known as polyostotic sclerosing histiocytosis) is a rare form of non-Langerhans cell histiocytosis (non-LCH) and until 2015 around 500 cases were reported [1].
Erdheim-Chester Disease (ECD) is a rare form of non-Langerhan cell histiocytosis that was first described by Chester in 1930 [1].