(Q46549133)

23 December 2017

title

Full access to medical records does not modify anxiety in cancer patients: results of a randomized study (English)

1 reference

23 December 2017

0 references

Gwenaelle Gravis

1

1 reference

23 December 2017

Cristel Protière

2

1 reference

23 December 2017

François Eisinger

3

1 reference

23 December 2017

Jean M Boher

4

1 reference

23 December 2017

Carole Tarpin

5

1 reference

23 December 2017

Diane Coso

6

1 reference

23 December 2017

Maria-Antonietta Cappiello

7

1 reference

23 December 2017

Jacques Camerlo

8

1 reference

23 December 2017

Dominique Genre

9

1 reference

23 December 2017

Patrice Viens

10

1 reference

23 December 2017

language of work or name

English

0 references

publication date

23 May 2011

1 reference

23 December 2017

published in

Cancer

1 reference

23 December 2017

volume

117

1 reference

23 December 2017

issue

20

1 reference

23 December 2017

page(s)

4796-4804

1 reference

23 December 2017

Information or advertising?

cites work

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Elaborating patient information with patients themselves: lessons from a cancer treatment focus group

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Patient participation in medical decision-making: a French study in adjuvant radio-chemotherapy for early breast cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Information needs and experiences: an audit of UK cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

No news is not good news: Information preferences of patients with cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Information needs of patients with cancer: results from a large study in UK cancer centres

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Women's preferences for discussion of prognosis in early breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Discordance between physicians' estimations and breast cancer patients' self-assessment of side-effects of chemotherapy: an issue for quality of care

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

The determinants and consequences of information seeking among cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Doctor-patient communication: a review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

The information needs and source preferences of women with breast cancer and their family members: a review of the literature published between 1988 and 1998.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Psychometric properties and responsiveness of the EORTC quality of Life Questionnaire (QLQ-C30) in patients with breast, ovarian and lung cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Reducing the negative impact of radiation therapy on functional status.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Information booklets about cancer: factors influencing patient satisfaction and utilization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Information and support for women following the primary treatment of breast cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Cancer patient preferences for communication of prognosis in the metastatic setting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Patient-centered care and breast cancer survivors’ satisfaction with information

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

Information and decision-making preferences of hospitalized adult cancer patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

7 January 2021

Psychosocial aspects of haematopoietic stem cell donation for allogeneic transplantation: how family donors cope with this experience

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

7 January 2021

Test/retest study of the European Organization for Research and Treatment of Cancer Core Quality-of-Life Questionnaire.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

7 January 2021

Breaking bad news about cancer: patients' preferences for communication

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

7 January 2021

Patient–physician interactions during early breast-cancer treatment: results from an international online survey

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26083

7 January 2021

https://api.crossref.org/works/10.1002%2FCNCR.26083

1 reference

7 January 2021

Identifiers

DOI

10.1002/CNCR.26083

1 reference

23 December 2017

1 reference

23 December 2017