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標(biāo)題: Titlebook: Asthma: Targeted Biological Therapies; Girolamo Pelaia,Alessandro Vatrella,Rosario Masell Book 2017 Springer International Publishing Swit [打印本頁]

作者: 突然    時間: 2025-3-21 16:03
書目名稱Asthma: Targeted Biological Therapies影響因子(影響力)




書目名稱Asthma: Targeted Biological Therapies影響因子(影響力)學(xué)科排名




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書目名稱Asthma: Targeted Biological Therapies網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Asthma: Targeted Biological Therapies被引頻次




書目名稱Asthma: Targeted Biological Therapies被引頻次學(xué)科排名




書目名稱Asthma: Targeted Biological Therapies年度引用




書目名稱Asthma: Targeted Biological Therapies年度引用學(xué)科排名




書目名稱Asthma: Targeted Biological Therapies讀者反饋




書目名稱Asthma: Targeted Biological Therapies讀者反饋學(xué)科排名





作者: Explosive    時間: 2025-3-21 22:11
Girolamo Pelaia,Alessandro Vatrella,Rosario MasellDescribes the rationale, mechanisms of action, and indications for use of biologics in asthma.Offers an excellent balance between basic science and analysis of clinical trials.Includes very clear illu
作者: 走調(diào)    時間: 2025-3-22 00:23
http://image.papertrans.cn/b/image/163550.jpg
作者: DRILL    時間: 2025-3-22 08:31
https://doi.org/10.1007/978-3-319-46007-9IL-13; IL-4; IL-5; airway remodelling in asthma; anti-IgE; anti-TNFalpha antibodies; cellular and molecula
作者: Etymology    時間: 2025-3-22 11:56
978-3-319-83417-7Springer International Publishing Switzerland 2017
作者: 不要不誠實(shí)    時間: 2025-3-22 14:42

作者: MAPLE    時間: 2025-3-22 18:18

作者: ARM    時間: 2025-3-23 00:44

作者: Endearing    時間: 2025-3-23 03:09
https://doi.org/10.1007/978-3-8348-9214-0airway structural cells, is a hallmark of asthma [1, 2]. Several inflammatory phenotypes of asthma have been characterized, which include eosinophilic, neutrophilic, mixed and paucigranulocytic patterns [3, 4]. Eosinophils are the inflammatory cells most frequently infiltrating the airways of asthma
作者: INCH    時間: 2025-3-23 06:22
https://doi.org/10.1007/978-3-658-30557-4es which involve all layers of the bronchial wall, including large and small airways [1, 2]. Such structural changes, collectively referred as airway remodelling, likely originate from repetitive cycles of tissue injury, causing subsequent cellular responses leading to abnormal repair [3]. Although
作者: FIS    時間: 2025-3-23 12:34

作者: 有權(quán)威    時間: 2025-3-23 16:56

作者: 尖酸一點(diǎn)    時間: 2025-3-23 18:31

作者: 潛伏期    時間: 2025-3-23 23:24

作者: Myocyte    時間: 2025-3-24 02:54

作者: 咽下    時間: 2025-3-24 09:29

作者: Manifest    時間: 2025-3-24 13:48

作者: agenda    時間: 2025-3-24 15:09
Book 2017 It offers an excellent balance between basic science and the analysis of clinical trials, updating readers with new developments that are changing the global scenario for targeted biological anti-asthma therapies, especially with regard to more severe disease. A range of therapies are considered, f
作者: 抱狗不敢前    時間: 2025-3-24 19:58

作者: 失眠癥    時間: 2025-3-25 00:54
Wolfgang B?ge,Wilfried Pla?mannrapies, many of which are undergoing advanced stages of clinical investigation, will probably lead in the next future to the introduction in real life of several other biologics indicated for asthma treatment [7–11].
作者: ironic    時間: 2025-3-25 05:28

作者: 評論性    時間: 2025-3-25 08:36
Conclusions and Future Perspectives,rapies, many of which are undergoing advanced stages of clinical investigation, will probably lead in the next future to the introduction in real life of several other biologics indicated for asthma treatment [7–11].
作者: 小木槌    時間: 2025-3-25 12:07
https://doi.org/10.1007/978-3-8348-9214-0 different responses to pharmacological therapies [5, 6]. The majority of asthmatic patients can achieve a good control of their symptoms using standard treatments including inhaled corticosteroids and bronchodilators such as β.-adrenergic agonists, as well as oral leukotriene inhibitors [7, 8].
作者: Diatribe    時間: 2025-3-25 18:17
https://doi.org/10.1007/978-3-658-30557-4 this key immunological discovery into the approval of the anti-IgE antibody omalizumab for the treatment of severe allergic asthma [7]. Indeed, omalizumab has been the first and for a long time the only biologic drug available in clinical practice for add-on therapy of uncontrolled asthma [8].
作者: 西瓜    時間: 2025-3-25 22:15
Wilfried Pla?mann,Detlef Schulzeroids, some subgroups of asthmatic subjects display persistent bronchial and/or blood eosinophilia, associated with an inadequate control of asthma [8]. Therefore, these patients can potentially benefit from additional therapies based on the use of biologic drugs targeting IL-5.
作者: Volatile-Oils    時間: 2025-3-26 00:52

作者: amnesia    時間: 2025-3-26 08:20

作者: 最小    時間: 2025-3-26 09:47
IL-5-Targeted Antibodies,eroids, some subgroups of asthmatic subjects display persistent bronchial and/or blood eosinophilia, associated with an inadequate control of asthma [8]. Therefore, these patients can potentially benefit from additional therapies based on the use of biologic drugs targeting IL-5.
作者: debase    時間: 2025-3-26 14:31

作者: 脫水    時間: 2025-3-26 19:00

作者: Anterior    時間: 2025-3-26 21:45
Wilfried Pla?mann,Detlef Schulzr ability to induce type 2 innate lymphoid cells (ILC2s) to produce T2-type cytokines such as IL-5, IL-9 and IL-13 [2]. Therefore, IL-25, IL-33 and TSLP are suitable targets for antiasthma biological therapies [3].
作者: 誹謗    時間: 2025-3-27 04:57

作者: 連鎖,連串    時間: 2025-3-27 05:18

作者: conflate    時間: 2025-3-27 13:03
Airway Remodelling in Asthma,es which involve all layers of the bronchial wall, including large and small airways [1, 2]. Such structural changes, collectively referred as airway remodelling, likely originate from repetitive cycles of tissue injury, causing subsequent cellular responses leading to abnormal repair [3]. Although
作者: eardrum    時間: 2025-3-27 14:15

作者: 詞匯表    時間: 2025-3-27 20:26

作者: Lucubrate    時間: 2025-3-28 01:15

作者: Kinetic    時間: 2025-3-28 05:41
,Anti-TNF-α Therapies, structural cells (Fig. 7.1) [1]. This pleiotropic cytokine is produced by several cell types including Th1 lymphocytes, macrophages and mast cells and induces the recruitment of neutrophils and eosinophils into the airways via up-regulation of epithelial and endothelial adhesion molecules [2, 3]. M
作者: 侵略    時間: 2025-3-28 06:52

作者: 寵愛    時間: 2025-3-28 13:01

作者: 自作多情    時間: 2025-3-28 18:35

作者: 并排上下    時間: 2025-3-28 22:29

作者: 多山    時間: 2025-3-29 01:28
https://doi.org/10.1007/978-3-8348-9214-0) (Fig. 2.1). In addition to being driven by adaptive immune responses, airway eosinophilia can also arise from innate immune mechanisms, which are mediated by intercellular communications involving dendritic cells, bronchial epithelial cells and innate lymphoid cells [7, 8]. Whilst bronchial eosino
作者: 痛苦一下    時間: 2025-3-29 04:50

作者: 疏忽    時間: 2025-3-29 08:09

作者: Proponent    時間: 2025-3-29 11:26
Airway Remodelling in Asthma, of chronic inflammation [6]. However, close interactions tightly connect the cellular and molecular mechanisms underpinning airway inflammation and remodelling (Fig. 3.1), and both pathologic processes certainly contribute together to induce bronchial hyperresponsiveness as well as asthma persisten
作者: contrast-medium    時間: 2025-3-29 19:33





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