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Idiopathic granulomatous hypophysitis: a systematic review of 82 cases in the literature
Idiopathic granulomatous hypophysitis (IGH) is a rare inflammatory disease of the pituitary. There is debate in the scientific literature as to whether IGH represents a continuum of disease with lymphocytic hypophysitis or has a distinct pathogenesis. Due to the rare nature of the disease, previous...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer US
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4085501/ https://ncbi.nlm.nih.gov/pubmed/23990347 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11102-013-0510-4 |
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