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Cancer Control, ISSN 1073-2748, 10/2014, Volume 21, Issue 4, pp. 328 - 334
Background: Langerhans cell histiocytosis (LCH) is a rare histiocytic disorder of unknown etiopathogenesis. Its clinical presentation is variable and ranges... 
THERAPY | GENE | ONCOLOGY | INVOLVEMENT | DISEASE | CENTRAL-NERVOUS-SYSTEM | MUTATIONS | EXPRESSION | TRANSPLANTATION | CHILDREN | FEATURES | Humans | Histiocytosis, Langerhans-Cell
Journal Article
Blood, ISSN 0006-4971, 06/2013, Volume 121, Issue 25, pp. 5006 - 5014
Journal Article
Cancer Treatment Reviews, ISSN 0305-7372, 2010, Volume 36, Issue 4, pp. 354 - 359
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 06/2018, Volume 78, Issue 6, pp. 1047 - 1056
A definitive diagnosis of Langerhans cell histiocytosis (LCH) requires a combination of clinical presentation, histology, and immunohistochemistry. The... 
cytarabine | clofarabine | cladribine | diabetes insipidus | Langerhans cell histiocytosis | vinblastine | BRAF | steroids
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 06/2018, Volume 78, Issue 6, pp. 1035 - 1044
Langerhans cell histiocytosis (LCH) is an inflammatory neoplasia of myeloid precursor cells driven by mutations in the mitogen-activated protein kinase... 
pathway myeloid neoplasia | BRAF | MAPK | Langerhans cell histiocytosis
Journal Article
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 08/2018, Volume 65, Issue 8, pp. e27079 - n/a
Journal Article