Autosomal dominant polycystic kidney disease: possibly the least silent cause of chronic kidney disease.

Torra, Roser; Pérez-Gómez, Maria Vanessa; Furlano, Mónica

Torra, Roser; Pérez-Gómez, Maria Vanessa; Furlano, Mónica.

Afiliação

Torra R; Inherited Kidney Diseases Nephrology Department, Fundació Puigvert IIB-Sant Pau Medicine Department, Universitat Autónoma de Barcelona, REDinREN, Barcelona, Spain.
Pérez-Gómez MV; Department of Nephrology and Hypertension, IIS-Fundacion Jimenez Diaz UAM, REDinREN, Madrid, Spain.
Furlano M; Inherited Kidney Diseases Nephrology Department, Fundació Puigvert IIB-Sant Pau Medicine Department, Universitat Autónoma de Barcelona, REDinREN, Barcelona, Spain.

Clin Kidney J ; 14(11): 2281-2284, 2021 Nov.

Article em En | MEDLINE | ID: mdl-34754424

Palavras-chave

ADPKD; assessment; pain; patient-reported outcome; trials

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Aspecto: Patient_preference Idioma: En Revista: Clin Kidney J Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Espanha

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