Literature DB >> 25256116

Personal reflections of a patient representative in an appraisal committee.

Cees Smit1.   

Abstract

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Year:  2015        PMID： 25256116     DOI： 10.1007/s40271-014-0086-8

Source DB:  PubMed          Journal:  Patient        ISSN： 1178-1653            Impact factor:   3.883


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  3 in total

1.  Developing Guidance on Ethics for Patient Groups Collecting and Reporting Patient Information for Health Technology Assessments.

Authors:  Ann N V Single; Anna M Scott; Janet Wale
Journal:  Patient       Date:  2016-02       Impact factor: 3.883

2.  The imperative for patient-centred research to develop better quality services in rare diseases.

Authors:  Karen Facey; Helle Ploug Hansen
Journal:  Patient       Date:  2015-02       Impact factor: 3.883

3.  Patient Perspectives on Novel Treatments in Haemophilia: A Qualitative Study.

Authors:  Erna C van Balen; Marjolein L Wesselo; Bridget L Baker; Marjan J Westerman; Michiel Coppens; Cees Smit; Mariëtte H E Driessens; Frank W G Leebeek; Johanna G van der Bom; Samantha C Gouw
Journal:  Patient       Date:  2020-04       Impact factor: 3.883
  3 in total

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