Developing a CKD registry in primary care: provider attitudes and input.
about
Chronic kidney disease care in the US safety net.Reducing CKD risks among vulnerable populations in primary care.Specialist and primary care physicians' views on barriers to adequate preparation of patients for renal replacement therapy: a qualitative study.The Kidney Awareness Registry and Education (KARE) study: protocol of a randomized controlled trial to enhance provider and patient engagement with chronic kidney disease.A national surveillance project on chronic kidney disease management in Canadian primary care: a study protocol
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Developing a CKD registry in primary care: provider attitudes and input.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
@tr
scientific article published on 02 December 2013
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vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Developing a CKD registry in primary care: provider attitudes and input.
@en
Developing a CKD registry in primary care: provider attitudes and input.
@nl
type
label
Developing a CKD registry in primary care: provider attitudes and input.
@en
Developing a CKD registry in primary care: provider attitudes and input.
@nl
prefLabel
Developing a CKD registry in primary care: provider attitudes and input.
@en
Developing a CKD registry in primary care: provider attitudes and input.
@nl
P2093
P2860
P1476
Developing a CKD registry in primary care: provider attitudes and input.
@en
P2093
Daniel Dohan
Dannielle McBride
Delphine S Tuot
Margaret A Handley
Neil R Powe
P2860
P304
P356
10.1053/J.AJKD.2013.10.012
P577
2013-12-02T00:00:00Z