罕见肺病

C. Robinson
{"title":"罕见肺病","authors":"C. Robinson","doi":"10.1093/MED/9780198837114.003.0040","DOIUrl":null,"url":null,"abstract":"Includes: Pathophysiology, classification, and lung involvement of alveolar microlithiasis and amyloidosis, hereditary haemorrhagic telangiectasia, idiopathic pulmonary haemosiderosis, Langerhans cell histiocytosis, clinical features, diagnosis, and management of lymphangioleiomyomatosis (LAM), primary ciliary dyskinesia (PCD), pathophysiology, clinical features, and diagnosis and treatment of pulmonary alveolar proteinosis (PAP), aetiology, diagnosis, management, and complications of pulmonary arteriovenous malformations (PAVMs), and recurrent respiratory papillomatosis.","PeriodicalId":447884,"journal":{"name":"Oxford Handbook of Respiratory Medicine","volume":"1 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rare lung diseases\",\"authors\":\"C. Robinson\",\"doi\":\"10.1093/MED/9780198837114.003.0040\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Includes: Pathophysiology, classification, and lung involvement of alveolar microlithiasis and amyloidosis, hereditary haemorrhagic telangiectasia, idiopathic pulmonary haemosiderosis, Langerhans cell histiocytosis, clinical features, diagnosis, and management of lymphangioleiomyomatosis (LAM), primary ciliary dyskinesia (PCD), pathophysiology, clinical features, and diagnosis and treatment of pulmonary alveolar proteinosis (PAP), aetiology, diagnosis, management, and complications of pulmonary arteriovenous malformations (PAVMs), and recurrent respiratory papillomatosis.\",\"PeriodicalId\":447884,\"journal\":{\"name\":\"Oxford Handbook of Respiratory Medicine\",\"volume\":\"1 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Oxford Handbook of Respiratory Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1093/MED/9780198837114.003.0040\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oxford Handbook of Respiratory Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/MED/9780198837114.003.0040","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

包括:肺泡微石症和淀粉样变性、遗传性出血性毛细血管扩张症、特发性肺血色素沉着症、朗格汉斯细胞组织细胞增多症的病理生理、分类和肺部损害、淋巴血管平滑肌瘤病(LAM)的临床特征、诊断和治疗、原发性纤毛运动障碍(PCD)、肺泡蛋白沉积症(PAP)的病理生理、临床特征和诊断和治疗、病因、诊断、治疗、肺动静脉畸形(pavm)和复发性呼吸道乳头状瘤病的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rare lung diseases
Includes: Pathophysiology, classification, and lung involvement of alveolar microlithiasis and amyloidosis, hereditary haemorrhagic telangiectasia, idiopathic pulmonary haemosiderosis, Langerhans cell histiocytosis, clinical features, diagnosis, and management of lymphangioleiomyomatosis (LAM), primary ciliary dyskinesia (PCD), pathophysiology, clinical features, and diagnosis and treatment of pulmonary alveolar proteinosis (PAP), aetiology, diagnosis, management, and complications of pulmonary arteriovenous malformations (PAVMs), and recurrent respiratory papillomatosis.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信