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1
Ciliary disorientation: a possible variant of primary ciliary dyskinesia.睫状体定向障碍:原发性睫状运动障碍的一种可能变体。
Thorax. 1993 Jul;48(7):770-1. doi: 10.1136/thx.48.7.770.
2
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Ciliary disorientation in patients with chronic upper respiratory tract inflammation.慢性上呼吸道炎症患者的睫状体方位异常。
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Nasal ciliary ultrastructure and function in patients with primary ciliary dyskinesia compared with that in normal subjects and in subjects with various respiratory diseases.原发性纤毛运动障碍患者的鼻纤毛超微结构和功能与正常受试者及各种呼吸系统疾病受试者的比较。
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Ciliary defects in healthy subjects, bronchiectasis, and primary ciliary dyskinesia.健康受试者、支气管扩张症和原发性纤毛运动障碍中的纤毛缺陷。
Am J Respir Crit Care Med. 1995 May;151(5):1559-67. doi: 10.1164/ajrccm.151.5.7735615.

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Am J Hum Genet. 2019 Feb 7;104(2):229-245. doi: 10.1016/j.ajhg.2018.12.009. Epub 2019 Jan 18.
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[Malignant tracheal tumors--surgical experiences in 6 patients with primary malignancies of the trachea. Current diagnosis and therapy].[恶性气管肿瘤——6例原发性气管恶性肿瘤的手术经验。当前的诊断与治疗]
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本文引用的文献

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Non-invasive sampling of nasal cilia for measurement of beat frequency and study of ultrastructure.用于测量摆动频率和超微结构研究的鼻纤毛无创采样。
Lancet. 1980 Sep 13;2(8194):564-5. doi: 10.1016/s0140-6736(80)91995-9.
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Alignment of cilia in immotile-cilia syndrome.
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Secondary ciliary dysfunction.继发性纤毛功能障碍
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Orientation of respiratory tract cilia in patients with primary ciliary dyskinesia, bronchiectasis, and in normal subjects.原发性纤毛运动障碍、支气管扩张症患者及正常受试者呼吸道纤毛的方向
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Absence of axonemal arms in nasal mucosa cilia in Kartagener's syndrome.
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A human syndrome caused by immotile cilia.一种由不动纤毛引起的人类综合征。
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睫状体定向障碍:原发性睫状运动障碍的一种可能变体。

Ciliary disorientation: a possible variant of primary ciliary dyskinesia.

作者信息

Rutman A, Cullinan P, Woodhead M, Cole P J, Wilson R

机构信息

Department of Thoracic Medicine, Royal Brompton National Heart and Lung Institute, London.

出版信息

Thorax. 1993 Jul;48(7):770-1. doi: 10.1136/thx.48.7.770.

DOI:10.1136/thx.48.7.770
PMID:8153929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC464673/
Abstract

Random ciliary orientation has recently been proposed as a variant of primary ciliary dyskinesia. We report a 12 year old boy with all the features of primary ciliary dyskinesia and absent nasal mucociliary clearance in whom repeated biopsies of the nasal epithelium showed normal ciliary beat frequency. The only abnormality discovered was disorientation of the central microtubules of his cilia.

摘要

随机纤毛定向最近被提出作为原发性纤毛运动障碍的一种变体。我们报告一名12岁男孩,具有原发性纤毛运动障碍的所有特征且鼻黏膜纤毛清除功能缺失,其鼻上皮的多次活检显示纤毛摆动频率正常。唯一发现的异常是其纤毛中央微管的定向异常。