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Néoplasie endocrinienne multiple type 1: à propos d'un cas
Multiple endocrine neoplasia type 1 (MEN1) is a rare disease, defined as a tumor developing in at least two endocrine glands including the anterior pituitary gland, the parathyroid glands and the duodenopancreatic endocrine tissue. This disorder, inherited in an autosomal dominant pattern, is caused...
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| Yayımlandı: | Pan Afr Med J |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The African Field Epidemiology Network
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6814935/ https://ncbi.nlm.nih.gov/pubmed/31692695 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2019.33.238.18053 |
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