(Q36532789)

English

Analysis of Published Criteria for Clinically Inactive Disease in a Large Juvenile Dermatomyositis Cohort Shows That Skin Disease Is Underestimated

scientific article published on 18 May 2015

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Analysis of Published Criteria for Clinically Inactive Disease in a Large Juvenile Dermatomyositis Cohort Shows That Skin Disease Is Underestimated (English)

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

dermatomyositis

0 references

author name string

Beverley Almeida

1

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Raquel Campanilho-Marques

2

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Katie Arnold

3

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Clarissa A Pilkington

4

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Lucy R Wedderburn

5

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Kiran Nistala

6

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Juvenile Dermatomyositis Research Group

7

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

publication date

18 May 2015

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Arthritis & Rheumatology

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

67

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

9

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

2495-2502

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

The PRINTO criteria for clinically inactive disease in juvenile dermatomyositis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4737199

30 September 2017

Measures of adult and juvenile dermatomyositis, polymyositis, and inclusion body myositis: Physician and Patient/Parent Global Activity, Manual Muscle Testing (MMT), Health Assessment Questionnaire (HAQ)/Childhood Health Assessment Questionnaire (C-

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4737199

30 September 2017

Validation of manual muscle testing and a subset of eight muscles for adult and juvenile idiopathic inflammatory myopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4737199

30 September 2017

International consensus outcome measures for patients with idiopathic inflammatory myopathies. Development and initial validation of myositis activity and damage indices in patients with adult onset disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4737199

30 September 2017

Medium- and long-term functional outcomes in a multicenter cohort of children with juvenile dermatomyositis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4737199

30 September 2017

Polymyositis and dermatomyositis (first of two parts)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4737199

30 September 2017

Polymyositis and dermatomyositis (second of two parts)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4737199

30 September 2017

Disease activity and prognostic factors in juvenile dermatomyositis: a long-term follow-up study applying the Paediatric Rheumatology International Trials Organization criteria for inactive disease and the myositis disease activity assessment tool.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4737199

21 September 2018

US incidence of juvenile dermatomyositis, 1995-1998: results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Registry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4737199

21 September 2018

International consensus guidelines for trials of therapies in the idiopathic inflammatory myopathies

1 reference

https://api.crossref.org/works/10.1002%2FART.39200

21 January 2018

Long-term outcome in patients with juvenile dermatomyositis: a cross-sectional follow-up study

1 reference

https://pubmed.ncbi.nlm.nih.gov/25988361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disease activity score for children with juvenile dermatomyositis: reliability and validity evidence

1 reference

https://pubmed.ncbi.nlm.nih.gov/25988361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A national registry for juvenile dermatomyositis and other paediatric idiopathic inflammatory myopathies: 10 years' experience; the Juvenile Dermatomyositis National (UK and Ireland) Cohort Biomarker Study and Repository for Idiopathic Inflammatory

1 reference

https://pubmed.ncbi.nlm.nih.gov/25988361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood dermatomyositis: factors predicting functional outcome and development of dystrophic calcification

1 reference

https://pubmed.ncbi.nlm.nih.gov/25988361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence of juvenile dermatomyositis: results from a nation-wide study

1 reference

https://pubmed.ncbi.nlm.nih.gov/25988361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile dermatomyositis at diagnosis: clinical characteristics of 79 children

1 reference

https://pubmed.ncbi.nlm.nih.gov/25988361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of validated disease activity and damage indices for the juvenile idiopathic inflammatory myopathies. II. The Childhood Myositis Assessment Scale (CMAS): a quantitative tool for the evaluation of muscle function. The Juvenile Dermatomyos

1 reference

https://pubmed.ncbi.nlm.nih.gov/25988361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/ART.39200

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

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