The importance of the general practitioner as an information source for patients with hereditary haemochromatosis-Reference-Cited by-同舟云学术

The importance of the general practitioner as an information source for patients with hereditary haemochromatosis

Published:2014-07 Issue:1 Volume:96 Page:86-92
ISSN:0738-3991
Container-title:Patient Education and Counseling
language:en
Short-container-title:Patient Education and Counseling

Author:

Teixeira Emerência,Borlido-Santos Júlio,Brissot Pierre,Butzeck Barbara,Courtois Françoise,Evans Robert W.,Fernau Janet,Nunes João Arriscado,Mullett Margaret,Paneque Milena,Pineau Brigitte,Porto Graça,Sorrill Robert,Sanchez Mayka,Swinkels Dorine W.,Toska Ketil,Varkonyi Judit

Funder

Fundação para a Ciência e Tecnologia

Biosense - Science engaging society: Life sciences, social sciences and publics

Publisher

Elsevier BV

Subject

General Medicine

Reference24 articles.

1. Patient-centredness in the consultation. 2, does it really make a difference?;Henbest;Fam Pract,1990

2. Patient-centredness: a conceptual framework and review of the empirical literature;Mead;Soc Sci Med,2000

3. What patients want;Bensing;Patient Educ Counsel,2013

4. Need for change in patient education: a Finnish survey from the patient's perspective;Johansson;Patient Educ Counsel,2003

5. EASL clinical practice guidelines for HFE hemochromatosis;J Hepatol,2010

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