Hyperphosphatemic Familial Tumoral Calcinosis: Odontostomatologic Management and Pathological Features
Author:
Affiliation:
1. Department of Emergency and Organ Transplantation, Pathological Anatomy, Aldo Moro University, Barii, Italy
Publisher
International Scientific Information, Inc.
Subject
General Medicine
Cited by 19 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. A Sole Case of the FGF23 Gene Mutation c.202A>G (p.Thr68Ala) Associated with Multiple Severe Vascular Aneurysms and a Hyperphosphatemic Variant of Tumoral Calcinosis—A Case Report;Life;2024-05-10
2. Three Siblings With a Rare Familial Hyperphosphatemia Syndrome: A Case Series;Cureus;2024-03-05
3. Canakinumab in addition to phosphate-binding and phosphaturia-inducing therapy were effective in achieving remission in a child with a large familial calcinotic tumour;Bone Reports;2023-12
4. Fully automated film mounting in dental radiography: a deep learning model;BMC Medical Imaging;2023-08-18
5. Dentoalveolar Alterations in an Adenine‐Induced Chronic Kidney Disease Mouse Model;Journal of Bone and Mineral Research;2023-05-27
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