A Molecular Classifier That Identifies Usual Interstitial Pneumonia in Transbronchial Biopsy Specimens of Patients With Interstitial Lung Disease.
作者信息
Raghu Ganesh, Colby Thomas V, Myers Jeffrey L, Steele Mark P, Benzaquen Sadia, Calero Karel, Case Amy H, Criner Gerard J, Nathan Steven D, Rai Navdeep S, Hagmeyer Lars, Davis J Russell, Bhorade Sangeeta M, Kennedy Giulia C, Gauher Umair A, Martinez Fernando J
机构信息
Center for Interstitial Lung Diseases, Department of Medicine and Laboratory Medicine, University of Washington Medical Center, University of Washington, Seattle, WA.
Department of Laboratory Medicine and Pathology (Emeritus), Mayo Clinic Arizona, Scottsdale, AZ.
出版信息
Chest. 2020 May;157(5):1391-1392. doi: 10.1016/j.chest.2019.10.061.
PMID:32386639
Abstract
摘要
相似文献
1
A Molecular Classifier That Identifies Usual Interstitial Pneumonia in Transbronchial Biopsy Specimens of Patients With Interstitial Lung Disease.
Chest. 2020 May;157(5):1391-1392. doi: 10.1016/j.chest.2019.10.061.
2
Use of a molecular classifier to identify usual interstitial pneumonia in conventional transbronchial lung biopsy samples: a prospective validation study.使用分子分类器鉴定常规经支气管肺活检样本中的寻常间质性肺炎：一项前瞻性验证研究。
Lancet Respir Med. 2019 Jun;7(6):487-496. doi: 10.1016/S2213-2600(19)30059-1. Epub 2019 Apr 1.
3
Prognostic value of transbronchial lung cryobiopsy for the multidisciplinary diagnosis of idiopathic pulmonary fibrosis: a retrospective validation study.经支气管肺冷冻活检对特发性肺纤维化多学科诊断的预后价值：一项回顾性验证研究。
Lancet Respir Med. 2020 Aug;8(8):786-794. doi: 10.1016/S2213-2600(20)30122-3.
4
Real-world utility of a genomic classifier in establishing a diagnosis of newly identified interstitial lung disease.基因组分类器在确定新诊断的间质性肺病中的实际应用。
Respir Med Res. 2023 Jun;83:100996. doi: 10.1016/j.resmer.2023.100996. Epub 2023 Jan 20.
5
Utility of a Molecular Classifier as a Complement to High-Resolution Computed Tomography to Identify Usual Interstitial Pneumonia.分子分类器作为高分辨率计算机断层扫描的补充，用于识别普通间质性肺炎的效用。
Am J Respir Crit Care Med. 2021 Jan 15;203(2):211-220. doi: 10.1164/rccm.202003-0877OC.
6
Centrilobular Fibrosis in Fibrotic (Chronic) Hypersensitivity Pneumonitis, Usual Interstitial Pneumonia, and Connective Tissue Disease-Associated Interstitial Lung Disease.纤维化（慢性）过敏性肺炎、特发性间质性肺炎和结缔组织病相关性间质性肺疾病中的中央性纤维化。
Arch Pathol Lab Med. 2020 Dec 1;144(12):1509-1516. doi: 10.5858/arpa.2019-0628-RA.
7
Review: interstitial lung disease associated with systemic sclerosis and idiopathic pulmonary fibrosis: how similar and distinct?综述：与系统性硬化症相关的间质性肺病和特发性肺纤维化：有何异同？
Arthritis Rheumatol. 2014 Aug;66(8):1967-78. doi: 10.1002/art.38702.
8
Mucins MUC5B and MUC5AC in Distal Airways and Honeycomb Spaces: Comparison among Idiopathic Pulmonary Fibrosis/Usual Interstitial Pneumonia, Fibrotic Nonspecific Interstitial Pneumonitis, and Control Lungs.远端气道和蜂窝状肺组织中的黏蛋白MUC5B和MUC5AC：特发性肺纤维化/普通型间质性肺炎、纤维化性非特异性间质性肺炎与对照肺组织的比较
Am J Respir Crit Care Med. 2016 Feb 15;193(4):462-4. doi: 10.1164/rccm.201507-1322LE.
9
Diagnosis and classification of idiopathic pulmonary fibrosis.特发性肺纤维化的诊断和分类。
Autoimmun Rev. 2014 Apr-May;13(4-5):508-12. doi: 10.1016/j.autrev.2014.01.037. Epub 2014 Jan 11.
10
Histopathologic findings of transbronchial biopsy in usual interstitial pneumonia.特发性间质性肺炎经支气管镜肺活检的组织病理学发现。
Pathol Int. 2010 May;60(5):373-7. doi: 10.1111/j.1440-1827.2010.02528.x.
Zotero 插件