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Multisystem Langerhans Cell Histiocytosis in Adult
Langerhans cell histiocytosis (LCH), is a rare disorder, clinically presents with heterogeneous manifestations, and has an unpredictable outcome. Commonly seen in infancy or early childhood, the disorder is characterized by proliferation of abnormal and clonal Langerhans cell in skin, bone, lymph no...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3312662/ https://ncbi.nlm.nih.gov/pubmed/22470214 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.92683 |
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