Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder-Reference-Cited by-同舟云学术

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Genetic aspects of primary hyperoxaluria: epidemiology, ethiology, pathogenesis, and clinical signs of the disorder

Published:2020-01-30 Issue: Volume:6_2020 Page:125-130
ISSN:1728-2985
Container-title:Urologiia
language:
Short-container-title:Urologiia

Author:

Filippova T.V. Filippova,Svetlichnaya D.V. Svetlichnaya,Rudenko V.I. Rudenko,Alyaev Y.G. Alyaev,Tadevosyan E.G. Tadevosyan,Azova M.M. Azova,Subbotina T.I. Subbotina,Gadzhieva Z.K. Gadzhieva,Asanov A.Y. Asanov,Khamidullin K.R. Khamidullin,Pushkarev A.M. Pushkarev,Litvinova M.M. Litvinova, , , , , ,

Publisher

Bionika Media

Subject

General Medicine

Cited by 1 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. Clinical experience of using denosumab in the treatment of hypercalcemia and oxalate osteopathy for a young patient with primary hyperoxaluria type 1.;Osteoporosis and Bone Diseases;2021-02-27

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