作者: 圓桶 時(shí)間: 2025-3-21 21:14
Fabien Maldonado,Sara Tomassetti,Jay H. Ryuons in Hilbert space due to M. Crouzeix. Moreover new quantitative results on asymptotic behaviour of Laplace transforms have been added. The references are updated and some errors have been corrected.978-3-0348-0327-4978-3-0348-0087-7Series ISSN 1017-0480 Series E-ISSN 2296-4886 作者: Tinea-Capitis 時(shí)間: 2025-3-22 03:17 作者: 易碎 時(shí)間: 2025-3-22 05:56
Helen J. Lachmann,Jennifer H. Pinneyons in Hilbert space due to M. Crouzeix. Moreover new quantitative results on asymptotic behaviour of Laplace transforms have been added. The references are updated and some errors have been corrected.978-3-0348-0327-4978-3-0348-0087-7Series ISSN 1017-0480 Series E-ISSN 2296-4886 作者: 中和 時(shí)間: 2025-3-22 11:12
Yann Nguyen,Lo?c Guillevinons in Hilbert space due to M. Crouzeix. Moreover new quantitative results on asymptotic behaviour of Laplace transforms have been added. The references are updated and some errors have been corrected.978-3-0348-0327-4978-3-0348-0087-7Series ISSN 1017-0480 Series E-ISSN 2296-4886 作者: 喃喃訴苦 時(shí)間: 2025-3-22 15:19
Christian Pagnoux,Alexandra Villa-Forteons in Hilbert space due to M. Crouzeix. Moreover new quantitative results on asymptotic behaviour of Laplace transforms have been added. The references are updated and some errors have been corrected.978-3-0348-0327-4978-3-0348-0087-7Series ISSN 1017-0480 Series E-ISSN 2296-4886 作者: 潛移默化 時(shí)間: 2025-3-22 20:46
Yosafe Wakwaya,Stephen K. Frankelons in Hilbert space due to M. Crouzeix. Moreover new quantitative results on asymptotic behaviour of Laplace transforms have been added. The references are updated and some errors have been corrected.978-3-0348-0327-4978-3-0348-0087-7Series ISSN 1017-0480 Series E-ISSN 2296-4886 作者: 關(guān)心 時(shí)間: 2025-3-22 22:11 作者: 國(guó)家明智 時(shí)間: 2025-3-23 03:11 作者: 惡臭 時(shí)間: 2025-3-23 06:14 作者: archenemy 時(shí)間: 2025-3-23 13:12
Joshua J. Solomon,Kevin Brown,Mary Kristen Demoruelleons in Hilbert space due to M. Crouzeix. Moreover new quantitative results on asymptotic behaviour of Laplace transforms have been added. The references are updated and some errors have been corrected.978-3-0348-0327-4978-3-0348-0087-7Series ISSN 1017-0480 Series E-ISSN 2296-4886 作者: cathartic 時(shí)間: 2025-3-23 14:05 作者: 洞穴 時(shí)間: 2025-3-23 18:06 作者: Fecal-Impaction 時(shí)間: 2025-3-24 00:21
y accessible information about the main orphan lung diseases, to aid clinicians in charge of patients with rare disease,or who consider the diagnosis of a rare disease in their patient. It is a practical, informative guide written by a team of international experienced authors in rare pulmonary diseases..978-3-031-12952-0978-3-031-12950-6作者: ALLAY 時(shí)間: 2025-3-24 06:22 作者: conscribe 時(shí)間: 2025-3-24 09:42 作者: 極端的正確性 時(shí)間: 2025-3-24 10:57 作者: 膠狀 時(shí)間: 2025-3-24 15:39
Challenges of Clinical Research in Orphan Diseasesl, economic, and scientific needs for research into rare diseases and suggest that a closer collaboration between experts, patient advocacy groups, policymakers, and industry is the only way forward for generating successful research in this field.作者: 留戀 時(shí)間: 2025-3-24 21:51 作者: colloquial 時(shí)間: 2025-3-24 23:31
Allergic Bronchopulmonary Aspergillosisas two of the four additional tests positive for a diagnosis: elevated eosinophil count, . skin test, . precipitins, or serum IgG for .. Guidelines for the diagnosis of ABPA in CF exist but have not been recently revised. Chest computed tomography (CT) images typically reveal bronchiectasis and hype作者: 良心 時(shí)間: 2025-3-25 05:17 作者: obscurity 時(shí)間: 2025-3-25 09:16
Granulomatosis with Polyangiitisneys (glomerulonephritis). A biopsy of the affected organ can support the diagnosis, as can detection in the serum of ANCAs with a proteinase 3 specificity (PR3-ANCAs) by enzyme-linked immunosorbent assay (ELISA). Important therapeutic advances have been made in the past three decades, and several m作者: nauseate 時(shí)間: 2025-3-25 12:07
Portopulmonary Hypertension and Hepatopulmonary Syndromederlying chronic liver disease, so it is imperative that clinicians maintain a high index of suspicion for these pulmonary vascular disorders when confronted with a dyspneic patient with hepatic disease (Table 11.1, Fig. 11.1). Both conditions significantly increase the morbidity and mortality of ch作者: 人類(lèi) 時(shí)間: 2025-3-25 19:07
Systemic Sclerosis and the Lunguppressive therapy, based on two controlled trials of cyclophosphamide and a comparison between cyclophosphamide and mycophenolate mofetil. Based on these data, the current consensus is that cyclophosphamide therapy is appropriate when SSc-ILD is extensive or overtly progressive with mycophenolate a作者: Adj異類(lèi)的 時(shí)間: 2025-3-25 20:31 作者: custody 時(shí)間: 2025-3-26 03:58 作者: habile 時(shí)間: 2025-3-26 05:17 作者: Wordlist 時(shí)間: 2025-3-26 10:22 作者: Bone-Scan 時(shí)間: 2025-3-26 13:16 作者: Glucose 時(shí)間: 2025-3-26 20:06
Vincent Cottin by buildings or other structures, or by vegetation, and the boundaries affect the attractiveness and the usefulness of the space, the extent to which it can be experienced, just as much as its dimensions, sub-divisions and content. Forming and defining units that can be perceived spatially in this 作者: thyroid-hormone 時(shí)間: 2025-3-26 21:37
Paolo Spagnolo,Nicol Bernardinelloth analysis of examples from international firms. An introductory look at the development thus far is followed by a systematic presentation of modes of representation in two, three, and four dimensions – in the plane, in space, and in the temporal process. The second section deals with the sequence 作者: Aggregate 時(shí)間: 2025-3-27 02:24 作者: dictator 時(shí)間: 2025-3-27 05:21 作者: 白楊魚(yú) 時(shí)間: 2025-3-27 10:42 作者: 北極熊 時(shí)間: 2025-3-27 15:22
Vincent Cottin,Luca Richeldi,Francis X. McCormackDeals comprehensively with the wide fields of rare pulmonary diseases.Clinically-orientated information for the clinician, together with “clinical vignettes”.Contains practical and easy-to-access info作者: misshapen 時(shí)間: 2025-3-27 20:42
Textbook 2023Latest editionematic disorders with lung involvement, interstitial lung diseases, and many other orphan conditions of the lungs are explored in this book. The progress and advances made in the field and the limited number of patients presenting each condition makes it very difficult for clinicians to be up-to-dat作者: 狗窩 時(shí)間: 2025-3-27 22:48 作者: enflame 時(shí)間: 2025-3-28 03:08 作者: Agility 時(shí)間: 2025-3-28 08:24 作者: Inflamed 時(shí)間: 2025-3-28 13:44
Eosinophilic Granulomatosis with Polyangiitisveral novel immunomodulatory drugs and biotherapies, the efficacies of which have been or are currently being evaluated. In this review, EGPA epidemiology, pathophysiology, clinical manifestations, outcomes, and the different therapeutic options now available, including therapeutic perspectives, are addressed.作者: 保存 時(shí)間: 2025-3-28 15:04
Lung Disease in Systemic Lupus Erythematosus, Myositis, Sj?gren’s Disease, and Mixed Connective Tisstion of this disease [4]. However, ILD can also present in SLE, SS, and MCTD with different clinical presentations, ranging from minimal significant pulmonary restriction to severe progressive pulmonary fibrosis [5, 6].作者: 合唱團(tuán) 時(shí)間: 2025-3-28 19:18
Interstitial Pneumonia with Autoimmune Features. Her high-resolution computed tomography images reveal evidence of diffuse lung disease suggestive of nonspecific interstitial pneumonia (NSIP) pattern (Fig. 15.1). Laboratory testing is notable only for a positive anti-nuclear antibody at high titer (1:1280). All other serologies and lab tests are normal.作者: 是剝皮 時(shí)間: 2025-3-29 01:21 作者: FLACK 時(shí)間: 2025-3-29 04:57 作者: Abbreviate 時(shí)間: 2025-3-29 07:49
Orphan Lung Diseases: From Definition to Organization of Caremanagement of their disease, and, as such, hope for the future is dim because so little research has been devoted to understanding such rare disorders in patients and improving their quality of life [1]. Their feeling of abandonment is intensified by comparisons with patients who suffer from common 作者: 吹氣 時(shí)間: 2025-3-29 13:09
Challenges of Clinical Research in Orphan Diseasesly, these conditions are generally poorly studied, frequently not well-understood, and often lack effective therapies. In recent years, the appreciation of the importance of research into rare diseases has grown considerably. In fact, rare disease research may not only benefit these patients directl作者: 夸張 時(shí)間: 2025-3-29 18:57 作者: VERT 時(shí)間: 2025-3-29 20:58 作者: 殘廢的火焰 時(shí)間: 2025-3-30 02:03
Orphan Tracheopathieslooked in patients presenting with nonspecific respiratory complaints. These tracheopathies include idiopathic subglottic stenosis (ISS), tracheobronchopathia osteochondroplastica (TPO), tracheomalacia (Mounier-Kuhn syndrome), tracheobronchomegaly, and tracheopathies associated with systemic disease作者: affinity 時(shí)間: 2025-3-30 05:10 作者: 不能逃避 時(shí)間: 2025-3-30 11:46
Eosinophilic Granulomatosis with Polyangiitistly affects small- and medium-sized vessels and is characterized by asthma and blood eosinophilia [1, 2]. Although anti-neutrophil cytoplasm antibody (ANCA) presence is not constant, EGPA is classified as a small-sized vessel, ANCA-associated vasculitis (AAV) [3]. Clinical phenotypes and pathogenic 作者: 聽(tīng)寫(xiě) 時(shí)間: 2025-3-30 14:38
Granulomatosis with Polyangiitisis also one of the three classical vasculitides associated with anti-neutrophil cytoplasm antibodies (ANCAs), along with microscopic polyangiitis and eosinophilic granulomatosis with polyangiitis. The incidence rate of GPA varies depending on the studies and countries between 2 and 30 cases per year作者: Carcinogenesis 時(shí)間: 2025-3-30 18:24
Alveolar Hemorrhagen. Patients commonly present with dyspnea, hemoptysis, anemia, diffuse radiographic pulmonary infiltrates, and hypoxemia. The severity can range from mild dyspnea to severe hypoxemic respiratory failure requiring mechanical ventilation. Diagnosis is frequently made at the time of bronchoscopy, when 作者: Kaleidoscope 時(shí)間: 2025-3-30 21:50
Pulmonary Involvement in Takayasu Arteritis and Beh?et Diseased blood vessels, and pathologically by the nature of the cellular infiltrate. Vasculitic involvement of pulmonary blood vessels may be secondary to infectious diseases, connective tissue diseases, malignancies, and hypersensitivity disorders or can be seen as a feature of primary small-vessel antine作者: habitat 時(shí)間: 2025-3-31 01:58
Portopulmonary Hypertension and Hepatopulmonary Syndromechronic liver disease. Despite being uncommon, these conditions have significant prognostic and therapeutic implications for patients, particularly those considering liver transplantation (LT). Mechanisms of disease pathogenesis in PoPH and HPS are poorly understood but involve vasoactive mediators 作者: Proclaim 時(shí)間: 2025-3-31 07:08 作者: 完成 時(shí)間: 2025-3-31 09:21 作者: CEDE 時(shí)間: 2025-3-31 15:06
Lung Disease in Systemic Lupus Erythematosus, Myositis, Sj?gren’s Disease, and Mixed Connective Tissmatosus (SLE), Sj?gren’s syndrome (SS), and Mixed Connective Tissue Disease (MCTD) can affect different levels of the respiratory tract, with a wide range of symptoms intensity, from asymptomatic to severe or life-threatening forms. Pleural disease is the most common lung manifestation in SLE and MC作者: 無(wú)辜 時(shí)間: 2025-3-31 19:13
