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Langerhans cell histiocytosis of the atlas in an adult

[Image: see text] Langerhans cell histiocytosis (LCH), formerly known as histiocytosis X, is a rare disorder (approximately 1:1,500,000 inhabitants) characterized by clonal proliferation and excess accumulation of pathologic Langerhans cells causing local or systemic effects. The exact etiology of L...

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Detalhes bibliográficos
Main Authors: Zhong, Wo Quan, Jiang, Liang, Ma, Qing Jun, Liu, Zhong Jun, Liu, Xiao Guang, Wei, Feng, Yuan, Hui Shu, Dang, Geng Ting
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2899733/
https://ncbi.nlm.nih.gov/pubmed/19844749
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00586-009-1172-9
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