Fatal pulmonary arterial hypertension (<scp>PAH</scp>): A rare association of anti‐MDA‐5 positive juvenile dermatomyositis-Reference-Cited by-同舟云学术

Fatal pulmonary arterial hypertension (PAH): A rare association of anti‐MDA‐5 positive juvenile dermatomyositis

Published:2024-05 Issue:5 Volume:27 Page:
ISSN:1756-1841
Container-title:International Journal of Rheumatic Diseases
language:en
Short-container-title:Int J of Rheum Dis

Author:

Shreyas R.¹,Patteri Anagha²,Hayagrivas M. B.²,Singla Tanya¹,Mohankumar Shivaprasad Pannasamudra³,Gupta Saurabh Kumar³,Jana Manisha⁴,Bagri Narendra Kumar¹^ORCID,Ramanan A. V.⁵

Affiliation:

1. Department of Paediatrics All India Institute of Medical Sciences New Delhi India

2. All India Institute of Medical Sciences New Delhi India

3. Department of Cardiology All India Institute of Medical Sciences New Delhi India

4. Department of Radiodiagnosis All India Institute of Medical Sciences New Delhi India

5. Department of Paediatric Rheumatology Bristol Royal Hospital for Children Bristol UK

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1756-185X.15180

Reference7 articles.

1. Dermatomyositis With Anti-MDA5 Antibodies: Bioclinical Features, Pathogenesis and Emerging Therapies

2. Pulmonary arterial hypertension in idiopathic inflammatory myopathies

3. Frequency, mutual exclusivity and clinical associations of myositis autoantibodies in a combined European cohort of idiopathic inflammatory myopathy patients

4. Histological heterogeneity in a large clinical cohort of juvenile idiopathic inflammatory myopathy: analysis by myositis autoantibody and pathological features

5. Disease characteristics and clinical outcomes of adults and children with anti-MDA-5 antibody-associated myositis: a prospective observational bicentric study