Development and initial validation of composite parent- and child-centered disease assessment indices for juvenile idiopathic arthritis
Maria Alessio
Arthritis Care & Research, 2011
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Assessment of disease activity in juvenile idiopathic arthritis. The number and the size of joints matter
Lisa Wernroth
The Journal of Rheumatology
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Relative responsiveness of condition specific and generic health status measures in juvenile idiopathic arthritis
Silvia Magni-manzoni
Annals of the Rheumatic Diseases, 2005
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The Short Arthritis Assessment Scale: a brief assessment questionnaire for rapid evaluation of arthritis severity in research and clinical practice
Fred Wolfe
The Journal of rheumatology, 2004
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Psychometric characteristics of outcome measures in juvenile idiopathic arthritis: A systematic review
Gillian Sanders Schmidler
Arthritis Care & Research, 2012
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Agreement between physicians and parents in rating functional ability of children with juvenile idiopathic arthritis
Elena Palmisani
Pediatric Rheumatology, 2007
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Development and validation of a new short and simple measure of physical function for juvenile idiopathic arthritis
G. Filocamo
Arthritis & Rheumatism, 2007
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Development and testing of reduced joint counts in juvenile idiopathic arthritis
silvia magni manzoni
The Journal of …, 2009
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Drivers of non-zero physician global scores during periods of inactive disease in juvenile idiopathic arthritis
Francesca Ridella
RMD Open, 2022
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The pediatric rheumatology quality of life scale: validation of the English version in a US cohort of juvenile idiopathic arthritis
Chris Feudtner
Pediatric rheumatology online journal, 2013
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Early detection of high disease activity in juvenile idiopathic arthritis by sequential monitoring of patients' health‐related quality of life scores
Peihua Qiu
Biometrical Journal
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Patient self-report RADAI (Rheumatoid Arthritis Disease Activity Index) joint counts on an MDHAQ (Multidimensional Health Assessment Questionnaire) in usual care of consecutive patients with rheumatic diseases other than rheumatoid arthritis
Isabel Castrejón
Arthritis Care & Research, 2013
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Assessment of quality of rheumatoid arthritis care requires joint count and/or patient questionnaire data not found in a usual medical record: examples from studies of premature mortality, changes in clinical status between 1985 and 2000, and a QUEST-RA global perspective
Theodore Pincus
Clinical and experimental rheumatology
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The difference in pain and overall well-being assessment between patients with juvenile idiopathic arthritis, their parents, and physicians in Ukraine
Halyna Pavlyshyn
Pediatria Polska
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Comparative measurement efficiency and sensitivity of five health status instruments for arthritis research
Matthew H Liang
Arthritis and Rheumatism, 1985
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Level of agreement between children, parents, and physicians in rating pain intensity in juvenile idiopathic arthritis
Marcia Bandeira, Silvia Magni-manzoni
Arthritis & Rheumatism, 2006
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Health of children with chronic arthritis: Relationship of different measures and the quality of parent proxy reporting
Murray Passo
Arthritis & Rheumatism, 2004
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Arthritis Impact Measurement Scales in a Community-Based Rheumatoid Arthritis Population
Pentti Nieminen
Clinical Rheumatology, 2000
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AIMS2. The Content and Properties of a Revised and Expanded Arthritis Impact Measurement Scales Health Status Questionnaire
Lewis Kazis
Arthritis & Rheumatism, 1992
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Most visits of most patients with rheumatoid arthritis to most rheumatologists do not include a formal quantitative joint count
Oscar Segurado
Annals of the Rheumatic Diseases, 2006
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A comparison of the measurement properties of the Juvenile Arthritis Functional Assessment Scale with the childhood health assessment questionnaire in daily practice
Peter Bekkering, Marion Rossum
Clinical Rheumatology, 2007
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RAPID3 (Routine Assessment of Patient Index Data 3), a rheumatoid arthritis index without formal joint counts for routine care: proposed severity categories compared to disease activity score and clinical disease activity index categories
Martin Bergman
2008
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Evidence for Updating the Core Domain Set of Outcome Measures for Juvenile Idiopathic Arthritis: Report from a Special Interest Group at OMERACT 2016
Julia Harris
The Journal of rheumatology, 2017
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Validation of the Brazilian version of the pediatric outcomes data collection instrument: a cross-sectional evaluation in children and adolescents with juvenile idiopathic arthritis
MARIA JAN CORINNE MARIANO
BMC Pediatrics, 2013
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Validity and reliability of self-reported arthritis
Charles Helmick
American Journal of Preventive Medicine, 2005
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Development of a disability measurement tool for juvenile rheumatoid arthritis. The juvenile arthritis functional assessment report for children and their parents
Steven Howe
Arthritis and Rheumatism, 1991
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PReS-FINAL-2116: Assessment of disease activity by patients with juvenile idiopathic arthritis and the parents compared to the assessment by pediatric rheumatologists
Jelte Bouma
Pediatric Rheumatology, 2013
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Health-related quality of life assessment in a group of children with juvenile idiopathic arthritis
Elham Hossny
2020
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Adding patient-reported outcomes to a multisite registry to quantify quality of life and experiences of disease and treatment for youth with juvenile idiopathic arthritis
Parissa K Salimian, Fatma Dedeoglu
Journal of Patient-Reported Outcomes, 2018
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Patient perceptions of foot disability in Juvenile Idiopathic Arthritis: a comparison of the juvenile arthritis foot disability index and the Oxford ankle foot questionnaire for children
Jill Ferrari
Journal of Foot and Ankle Research, 2015
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