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A case of anti-Th/To antibody-positive interstitial lung disease and pulmonary arterial hypertension that does not meet the classification criteria of systemic sclerosis. Comment on the article by Moschetti et al.

Eri SakaidaYuta YamashitaYoshinao MuroMirai SawaTeruyuki MitsumaMasashi Akiyama
Published in: Clinical and experimental rheumatology (2024)
Keyphrases
  • pulmonary arterial hypertension
  • systemic sclerosis
  • interstitial lung disease
  • pulmonary artery
  • pulmonary hypertension
  • deep learning
  • machine learning
  • idiopathic pulmonary fibrosis