Phosphaturic mesenchymal tumor (PMT): Exceptionally rare disease, yet crucial not to miss-Reference-Cited by-同舟云学术

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Phosphaturic mesenchymal tumor (PMT): Exceptionally rare disease, yet crucial not to miss

Published:2017 Issue:3 Volume:7 Page:32-37
ISSN:2236-1960
Container-title:Autopsy and Case Reports
language:
Short-container-title:Autops. Case Rep.

Author:

Ghorbani-Aghbolaghi Amir,Darrow Morgan Angus,Wang Tao

Publisher

Editora Cubo

Link

http://s3.amazonaws.com/host-article-assets/autopsy/59ca374b0e882503407c305c/fulltext.pdf

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Superficial acral calcified chondroid mesenchymal neoplasm harboring an FN1::FGFR2 fusion and review of the literature;Journal of Cutaneous Pathology;2024-02-08

2. Prolonged generalized osteomalacia associated with a sinonasal cavity phosphaturic mesenchymal tumor: A case report;Clinical Case Reports;2024-01-30

3. Detection of recurrent phosphaturic mesenchymal tumors by using Ga-68 DOTATATE PET/CT;The European Research Journal;2024-01-04

4. Phosphaturic mesenchymal tumor with de novo liver metastases: a case report and literature review;Therapeutic Advances in Medical Oncology;2024-01

5. Phosphaturic mesenchymal tumor: Clinicopathological features with outcomes in 10 patients with review of literature;Indian Journal of Pathology and Microbiology;2023-11-09

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