Mineral bone disease in autosomal dominant polycystic kidney disease

Mice with disruption of Pkd1 in osteoblasts demonstrate reduced bone mineral density, trabecular bone volume and cortical thickness. To date, the bone phenotype in adult patients with autosomal dominant polycystic kidney disease (ADPKD) with stage I and II chronic kidney disease has not been investi...

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Publicat a:Kidney Int
Autors principals: Gitomer, Berenice, Pereira, Renata, Salusky, Isidro B., Stoneback, Jason W., Isakova, Tamara, Cai, Xuan, Dalrymple, Lorien S., Ofsthun, Norma, You, Zhiying, Malluche, Harmut H., Maddux, Franklin, George, Diana, Torres, Vicente, Chapman, Arlene, Steinman, Theodore I., Wolf, Myles, Chonchol, Michel
Format: Artigo
Idioma:Inglês
Publicat: 2020
Matèries:
Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7993988/
https://ncbi.nlm.nih.gov/pubmed/32926884
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.kint.2020.07.041
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