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J-GLOBAL ID:202102218696001228   Reference number:21A0327567

Inhaled Hypertonic Saline in Siblings with Primary Ciliary Dyskinesia

原発性線毛機能不全症同胞例に対する高張食塩水吸入療法
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Volume: 125  Issue:Page: 52-58  Publication year: Jan. 01, 2021 
JST Material Number: F0896A  ISSN: 0001-6543  CODEN: NIPOA  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Drug therapy(=pharmacotherapy)for respiratory system diseases  ,  Treatment for congenital diseases,deformities. 
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Reference (15):
  • Bush A, Cole P, Hariri M, et al. Primary ciliary dyskinesia ; diagnosis and standards of care. Eur Respir J 1998 ; 12 : 982-988.
  • 宮川知士.原発性線毛機能不全.『小児内科』『小児外科』編集委員会共編.小児疾患診療のための病態生理.第4版.東京:東京医学社,2008:102-105.
  • Elkins MR, Robinson M, Rose BR, et al. A controlled trial of long-term inhaled hypertonic saline in patients with cystic fibrosis. N Engl J Med 2006 ; 354 : 229-240.
  • Paff T, Daniels JM, Weersink EJ, et al. A randomised controlled proof-of-concept study on the effect of inhaled hypertonic saline on quality of life in primary ciliary dyskinesia. Eur Respir J 2017 ; 49 ; 1601770.
  • Behan L, Dimitrov BD, Kuehni CE, et al. PICADAR : a diagnostic predictive tool for primary ciliary dyskinesia. Eur Respir J 2016 ; 47 : 1103-1112.
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