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Transformation sarcomateuse de la maladie de Recklinghausen
Neurofibromatosis type I is a common genetic disease. Affected patients are 4 times more likely to develop a tumor. Most tumors are benign (neurofibromas). Although these rarely result in malignant tumors, they represent the leading cause of death in patients, thus making neurofibromatosis type I a...
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| Gepubliceerd in: | Pan Afr Med J |
|---|---|
| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
The African Field Epidemiology Network
2021
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8164437/ https://ncbi.nlm.nih.gov/pubmed/34104304 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2021.38.256.16742 |
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