Performance of the Patient-Reported Outcomes Measurement Information System-29 in scleroderma: a Scleroderma Patient-centered Intervention Network Cohort Study

Psychosocial Aspects of Scleroderma

(2015) Linda Kwakkenbos et al.   RHEUMATIC DISEASE CLINICS OF NORTH AMERICA

Major Depression Diagnoses Among Patients With Systemic Sclerosis: Baseline and One-Month Followup

(2015) Brett D. Thombs et al.   ARTHRITIS CARE & RESEARCH

Longitudinal Evaluation of PROMIS-29 and FACIT-Dyspnea Short Forms in Systemic Sclerosis

(2014) M. E. Hinchcliff et al.   JOURNAL OF RHEUMATOLOGY

Prevalence of current, 12-month and lifetime major depressive disorder among patients with systemic sclerosis

(2014) L. R. Jewett et al.   RHEUMATOLOGY

2013 Classification Criteria for Systemic Sclerosis: An American College of Rheumatology/European League Against Rheumatism Collaborative Initiative

(2013) Frank van den Hoogen et al.   ARTHRITIS AND RHEUMATISM

The Scleroderma Patient-centered Intervention Network (SPIN) Cohort: protocol for a cohort multiple randomised controlled trial (cmRCT) design to support trials of psychosocial and rehabilitation interventions in a rare disease context

(2013) Linda Kwakkenbos et al.   BMJ Open

Utility of the Patient Health Questionnaire-9 to Assess Suicide Risk in Patients With Systemic Sclerosis

(2012) Ilya Razykov et al.   ARTHRITIS CARE & RESEARCH

Feasibility and Construct Validity of PROMIS and “Legacy” Instruments in an Academic Scleroderma Clinic

(2011) Dinesh Khanna et al.   VALUE IN HEALTH

Validity of two new patient-reported outcome measures in systemic sclerosis: Patient-reported outcomes measurement information system 29-item health profile and functional assessment of chronic illness therapy-dyspnea short form

(2011) Monique Hinchcliff et al.   ARTHRITIS CARE & RESEARCH

The future of measuring patient-reported outcomes in rheumatology: Patient-Reported Outcomes Measurement Information System (PROMIS)

(2011) Dinesh Khanna et al.   ARTHRITIS CARE & RESEARCH

The COSMIN checklist for assessing the methodological quality of studies on measurement properties of health status measurement instruments: an international Delphi study

(2010) Lidwine B. Mokkink et al.   QUALITY OF LIFE RESEARCH

Comparison of the PHQ-9 and CES-D depression scales in systemic sclerosis: internal consistency reliability, convergent validity and clinical correlates

(2010) K. Milette et al.   RHEUMATOLOGY

Frequency and impact of symptoms experienced by patients with systemic sclerosis: results from a Canadian National Survey

(2010) M. Bassel et al.   RHEUMATOLOGY

Psychological health and well-being in systemic sclerosis: State of the science and consensus research agenda

(2010) Brett D. Thombs et al.   ARTHRITIS CARE & RESEARCH

Health-related quality of life in systemic sclerosis: A systematic review

(2009) Marie Hudson et al.   ARTHRITIS AND RHEUMATISM

The PHQ-8 as a measure of current depression in the general population

(2008) Kurt Kroenke et al.   JOURNAL OF AFFECTIVE DISORDERS