Literature DB >> 17333563

The importance of patient-reported outcomes...it's all about the patients.

Linda Bren.   

Abstract

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Year:  2006        PMID： 17333563

Source DB:  PubMed          Journal:  FDA Consum        ISSN： 0362-1332


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  19 in total

1.  Challenges assessing clinical endpoints in early Huntington disease.

Authors:  Jane S Paulsen; Chiachi Wang; Kevin Duff; Roger Barker; Martha Nance; Leigh Beglinger; David Moser; Janet K Williams; Sheila Simpson; Douglas Langbehn; Daniel P van Kammen
Journal:  Mov Disord       Date:  2010-11-15       Impact factor: 10.338

2.  Automated monitoring of symptoms during ambulatory chemotherapy and oncology providers' use of the information: a randomized controlled clinical trial.

Authors:  Kathi H Mooney; Susan L Beck; Robert H Friedman; Ramesh Farzanfar; Bob Wong
Journal:  Support Care Cancer       Date:  2014-04-01       Impact factor: 3.603

3.  Logistics of collecting patient-reported outcomes (PROs) in clinical practice: an overview and practical examples.

Authors:  Matthias Rose; Andrea Bezjak
Journal:  Qual Life Res       Date:  2009-01-20       Impact factor: 4.147

4.  Early Detection of Huntington Disease.

Authors:  Jane S Paulsen
Journal:  Future Neurol       Date:  2010-01

Review 5.  Assessment of bias in outcomes reported in trials on pneumonia: a systematic review.

Authors:  T Avni; S Shiber-Ofer; L Leibovici; M Paul
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2013-12-19       Impact factor: 3.267

6.  Earliest functional declines in Huntington disease.

Authors:  Leigh J Beglinger; Justin J F O'Rourke; Chiachi Wang; Douglas R Langbehn; Kevin Duff; Jane S Paulsen
Journal:  Psychiatry Res       Date:  2010-05-15       Impact factor: 3.222

Review 7.  Patient-reported outcome measures in inflammatory bowel disease.

Authors:  Wael El-Matary
Journal:  Can J Gastroenterol Hepatol       Date:  2014-11

8.  Health-related quality of life in children with hemifacial microsomia: parent and child perspectives.

Authors:  Mary A Khetani; Brent R Collett; Matthew L Speltz; Martha M Werler
Journal:  J Dev Behav Pediatr       Date:  2013 Nov-Dec       Impact factor: 2.225

9.  Quality-of-life in Charcot-Marie-Tooth disease: the patient's perspective.

Authors:  Nicholas E Johnson; Chad R Heatwole; Nuran Dilek; Janet Sowden; Callyn A Kirk; Denise Shereff; Michael E Shy; David N Herrmann
Journal:  Neuromuscul Disord       Date:  2014-06-27       Impact factor: 4.296

10.  Enhancing measurement in health outcomes research supported by Agencies within the US Department of Health and Human Services.

Authors:  Bryce B Reeve; Laurie B Burke; Yen-pin Chiang; Steven B Clauser; Lisa J Colpe; Jeffrey W Elias; John Fleishman; Ann A Hohmann; Wendy L Johnson-Taylor; William Lawrence; Claudia S Moy; Louis A Quatrano; William T Riley; Barbara A Smothers; Ellen M Werner
Journal:  Qual Life Res       Date:  2007-05-26       Impact factor: 4.147
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