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Limitations of Nasal Nitric Oxide Testing in Primary Ciliary Dyskinesia.

作者信息

Shapiro Adam J, Davis Stephanie D, Leigh Margaret W, Knowles Michael R, Lavergne Valery, Ferkol Thomas

机构信息

Montreal Children's HospitalMontreal, Quebec, Canada.

University of North CarolinaChapel Hill, North Carolina.

出版信息

Am J Respir Crit Care Med. 2020 Aug 1;202(3):476-477. doi: 10.1164/rccm.202003-0835LE.

DOI:10.1164/rccm.202003-0835LE
PMID:32329626
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7397801/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd3c/7397801/37dcb3fe0e7c/rccm.202003-0835LEf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd3c/7397801/37dcb3fe0e7c/rccm.202003-0835LEf1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd3c/7397801/37dcb3fe0e7c/rccm.202003-0835LEf1.jpg

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本文引用的文献

1
Nasal Nitric Oxide Measurement in Primary Ciliary Dyskinesia. A Technical Paper on Standardized Testing Protocols.原发性纤毛运动障碍的鼻一氧化氮测量。标准化测试方案技术论文。
Ann Am Thorac Soc. 2020 Feb;17(2):e1-e12. doi: 10.1513/AnnalsATS.201904-347OT.
2
Response.反应
Chest. 2019 Nov;156(5):1033-1034. doi: 10.1016/j.chest.2019.07.001.
3
Nasal Nitric Oxide in Primary Immunodeficiency and Primary Ciliary Dyskinesia: Helping to Distinguish Between Clinically Similar Diseases.原发性免疫缺陷病和原发性纤毛运动障碍中鼻内一氧化氮：有助于鉴别临床相似疾病。
原发性纤毛运动障碍或活化磷脂酰肌醇3-激酶δ综合征患者的重叠临床表型
J Pediatr. 2025 May;280:114499. doi: 10.1016/j.jpeds.2025.114499. Epub 2025 Feb 6.
4
Primary Ciliary Dyskinesia: A Clinical Review.原发性纤毛运动障碍：临床综述。
Cells. 2024 Jun 4;13(11):974. doi: 10.3390/cells13110974.
5
The utility of nasal nitric oxide in the diagnostic evaluation of primary ciliary dyskinesia.鼻腔一氧化氮在原发性纤毛运动障碍诊断评估中的应用。
Pediatr Pulmonol. 2024 May;59(5):1410-1417. doi: 10.1002/ppul.26929. Epub 2024 Feb 21.
6
An Under-Recognized Disease: A Rare Case of Idiopathic CD4 Lymphopenia Mislabeled as Primary Ciliary Dyskinesia.一种未被充分认识的疾病：一例被误诊为原发性纤毛运动障碍的特发性CD4淋巴细胞减少症罕见病例。
Children (Basel). 2022 Oct 7;9(10):1534. doi: 10.3390/children9101534.
7
A Novel Homozygous Variant in GAS2L2 in Two Sisters with Primary Ciliary Dyskinesia.两姐妹原发性纤毛运动障碍中 GAS2L2 的新型纯合变异。
Intern Med. 2022;61(18):2765-2769. doi: 10.2169/internalmedicine.8884-21. Epub 2022 Sep 15.
8
Recessive Mutations in Cause Primary Ciliary Dyskinesia with Normal Ciliary Ultrastructure.某基因的隐性突变导致具有正常纤毛超微结构的原发性纤毛运动障碍。
Am J Respir Cell Mol Biol. 2022 Sep;67(3):409-413. doi: 10.1165/rcmb.2022-0032LE.
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An international survey on nasal nitric oxide measurement practices for the diagnosis of primary ciliary dyskinesia.一项关于用于原发性纤毛运动障碍诊断的鼻一氧化氮测量实践的国际调查。
ERJ Open Res. 2022 Apr 4;8(2). doi: 10.1183/23120541.00708-2021. eCollection 2022 Apr.
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Diagnosis of primary ciliary dyskinesia: discrepancy according to different algorithms.原发性纤毛运动障碍的诊断：不同算法下的差异
ERJ Open Res. 2021 Nov 1;7(4). doi: 10.1183/23120541.00353-2021. eCollection 2021 Oct.
J Clin Immunol. 2019 Feb;39(2):216-224. doi: 10.1007/s10875-019-00613-8. Epub 2019 Mar 26.
4
Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline.原发性纤毛运动障碍的诊断。美国胸科学会临床实践指南。
Am J Respir Crit Care Med. 2018 Jun 15;197(12):e24-e39. doi: 10.1164/rccm.201805-0819ST.
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Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia.将鼻一氧化氮测量标准化作为原发性纤毛运动障碍的一种测试方法。
Ann Am Thorac Soc. 2013 Dec;10(6):574-81. doi: 10.1513/AnnalsATS.201305-110OC.