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PedAM

Pediatric Disease Annotations & Medicines




Disease dermatomyositis
Phenotype C0024115|lung disease
Sentences 23
PubMedID- 25698373 Rapidly progressive interstitial lung disease (rp-ild) in patients with clinically amyopathic dermatomyositis (cadm) associated with antibodies to melanoma differentiation-associated gene5 (mda5) results in a high mortality rate.
PubMedID- 25346167 Anti-transcription intermediary factor 1-gamma antibody-positive clinically amyopathic dermatomyositis complicated by interstitial lung disease and breast cancer.
PubMedID- 22931947 [clinical characteristics of juvenile dermatomyositis complicated with interstitial lung disease].
PubMedID- 20506189 Conclusion: these promising data indicate that mycophenolate mofetil may be a useful therapy for interstitial lung disease in patients with dermatomyositis, but larger studies are needed to more definitively evaluate the role of this medication in therapy.
PubMedID- 26328651 Rapidly progressive interstitial lung disease associated with dermatomyositis treated with combination of immunosuppressive therapy, direct hemoperfusion with a polymyxin b immobilized fiber column and intravenous immunoglobulin.
PubMedID- 25888887 Serum progranulin levels are elevated in dermatomyositis patients with acute interstitial lung disease, predicting prognosis.
PubMedID- 22863719 Pilot study of interleukin-27 in pathogenesis of dermatomyositis and polymyositis: associated with interstitial lung diseases.
PubMedID- 23569020 Objective: : to study the clinical features of interstitial lung disease (ild) in patients with dermatomyositis and factors related to its development.
PubMedID- 23423441 This diagnosis should always come to mind in patients that present with signs of myositis, dermatomyositis, or polymyositis associated with interstitial lung disease.
PubMedID- 23158422 Objective: to explore the possible diagnostic values of serum surfactant protein-a (sp-a) and surfactant protein-d (sp-d) for interstitial lung diseases (ild) in patients with polymyositis or dermatomyositis (pm/dm).
PubMedID- 20827201 A rare form of ild with a very poor prognosis, acute and rapidly progressive lung disease, is strongly associated with clinically amyopathic dermatomyositis (cadm) and a novel - anti-cadm-140 auto-antibody.
PubMedID- 24142786 [interstitial lung disease in patients with polymyositis and dermatomyositis--report of three cases].
PubMedID- 23983712 He was suspected of rapidly progressing interstitial lung disease with dermatomyositis and transferred to our hospital.
PubMedID- 20800454 Serum tarc/ccl17 levels are increased in dermatomyositis associated with interstitial lung disease.
PubMedID- 21748914 Subsequently, a diagnosis of amyopathic dermatomyositis with interstitial lung disease and pneumomediastinum was made.
PubMedID- 26459323 Serum il8 and mrna level of cd11b in circulating neutrophils are increased in clinically amyopathic dermatomyositis with active interstitial lung disease.
PubMedID- 22781896 [a clinical analysis of dermatomyositis with interstitial lung disease in 20 patients].
PubMedID- 26101728 Incidence and impact of interstitial lung disease and malignancy in patients with polymyositis, dermatomyositis, and clinically amyopathic dermatomyositis: a retrospective cohort study.
PubMedID- 25622670 Objective: to explore the clinical features and prognosis of dermatomyositis patients with interstitial lung disease (ild) as an initial manifestation.
PubMedID- 23400027 Limitations to the 6-minute walk test in dermatomyositis with interstitial lung disease in comparison with idiopathic interstitial pneumonia.
PubMedID- 24325117 Objective: to investigate the clinical features and risk factors associated with interstitial lung disease (ild) in patients with classic dermatomyositis (classic dm) or clinical amyopathic dermatomyositis (cadm).
PubMedID- 25433590 [interstitial lung disease-associated with amyopathic dermatomyositis and anti-mda5 autoantibodies].
PubMedID- 22325787 Clinical factors to predict a poor prognosis and refractory disease in patients with polymyositis and dermatomyositis associated with interstitial lung disease.

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