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Langerhans-Cell Histiocytosis

Langerhans-Cell Histiocytosis

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6334777

Langerhans-Cell Histiocytosis

About this item

Full title

Langerhans-Cell Histiocytosis

Publisher

United States: Massachusetts Medical Society

Journal title

The New England journal of medicine, 2018-08, Vol.379 (9), p.856-868

Language

English

Formats

Publication information

Publisher

United States: Massachusetts Medical Society

More information

Scope and Contents

Contents

A spectrum of diseases formerly known as histiocytosis X and now called Langerhans-cell histiocytosis is characterized by ERK pathway activation (including
BRAF
V600E mutations) and diverse clinical manifestations involving bone, skin, lung, and pituitary.

Alternative Titles

Full title

Langerhans-Cell Histiocytosis

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6334777

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6334777

Other Identifiers

ISSN

0028-4793

E-ISSN

1533-4406

DOI

10.1056/NEJMra1607548

How to access this item