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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Detalhes bibliográficos
Publicado no:Kidney Int
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
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Article
Acesso em linha: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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