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Titlebook: Orphan Lung Diseases; A Clinical Guide to Vincent Cottin,Jean-Francois Cordier,Luca Richeldi Book 20151st edition Springer-Verlag London 2

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發(fā)表于 2025-3-21 19:08:49 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Orphan Lung Diseases
副標(biāo)題A Clinical Guide to
編輯Vincent Cottin,Jean-Francois Cordier,Luca Richeldi
視頻videohttp://file.papertrans.cn/705/704675/704675.mp4
概述Contains practical and easy-to-access information on the diagnostic approach, with illustrations of chest imaging (mostly high resolution computed tomography).Assists the reader in evoking and confirm
圖書封面Titlebook: Orphan Lung Diseases; A Clinical Guide to  Vincent Cottin,Jean-Francois Cordier,Luca Richeldi Book 20151st edition Springer-Verlag London 2
描述Orphan Lung Diseases: A Clinical Guide to Rare Lung Disease provides a comprehensive, clinically focused textbook on rare and so-called ‘orphan’ pulmonary diseases. The book is oriented towards the diagnostic approach, including manifestations suggesting the disease, diagnostic criteria, methods of diagnostic confirmation, and differential diagnosis, with an overview of management.
出版日期Book 20151st edition
關(guān)鍵詞Bronchiolitis; Interstitial; Pulmonary; Tracheopathies; Vasculitides
版次1
doihttps://doi.org/10.1007/978-1-4471-2401-6
isbn_softcover978-1-4471-6953-6
isbn_ebook978-1-4471-2401-6
copyrightSpringer-Verlag London 2015
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 20:16:14 | 只看該作者
板凳
發(fā)表于 2025-3-22 00:39:38 | 只看該作者
Exogenous Lipoid Pneumonia,o show presence of intrapulmonary oil, such as bronchoalveolar lavage or histological specimens of which fat stains will be used..Endogenous lipid pneumonia must be eliminated..Early recognition and discontinuation of exposure are essential to prevent the lesions from evolving towards fibrosis and respiratory failure.
地板
發(fā)表于 2025-3-22 05:58:25 | 只看該作者
Pulmonary Alveolar Proteinosis,is. Whole-lung lavage is the most effective, rapid and demonstrated therapy, especially for autoimmune disease. Novel therapies targeting alveolar macrophages (recombinant GM-CSF therapy) or anti-GM-CSF antibodies (rituximab, plasmapheresis) may be of interest.
5#
發(fā)表于 2025-3-22 09:14:17 | 只看該作者
The Challenges of Clinical Research in Orphan Diseases,iseases field..In this chapter we discuss ethical, social, economic and scientific needs for research into rare diseases and suggest that an even closer collaboration between patients, authorities and industry represents the way forward for generating more research in this field.
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發(fā)表于 2025-3-22 16:06:21 | 只看該作者
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發(fā)表于 2025-3-22 17:28:24 | 只看該作者
Amyloidosis and the Respiratory Tract,Encouragingly, specific drug therapies designed to stabilize amyloid precursor proteins, interfere with amyloid fibrillogenesis and accelerate the clearance of tissue amyloid deposits are all on the horizon.
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發(fā)表于 2025-3-23 01:16:23 | 只看該作者
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發(fā)表于 2025-3-23 05:06:59 | 只看該作者
Orphan Lung Diseases from Definition to Organisation of Care, the more distressing manifestations. The patients with rare diseases thus feel abandoned and orphan when comparing with patients with common diseases who benefit from extensive research worldwide and continuous drug development.
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發(fā)表于 2025-3-23 09:31:35 | 只看該作者
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