Respiratory medicine CME最新文献

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Pulmonary fibrosis in systemic sclerosis: Diagnosis & management 系统性硬化症中的肺纤维化:诊断与治疗
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.09.016
Howard M. Branley
{"title":"Pulmonary fibrosis in systemic sclerosis: Diagnosis & management","authors":"Howard M. Branley","doi":"10.1016/j.rmedc.2009.09.016","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.09.016","url":null,"abstract":"<div><p>Systemic sclerosis is a fascinating, although uncommon condition. However, fibrosing alveolitis in systemic sclerosis patients is common and is associated with significant morbidity and mortality. Investigations assist, not only with diagnosis, but also with assessment of disease severity and assessment of the likelihood of disease progression, thus helping to identify those requiring closer medical supervision. Treatment of fibrosing alveolitis in systemic sclerosis is complex, as the risks of some therapies may outweigh the potential benefits, and for those with advanced disease there is a lack of donor organs available for transplantation. Great strides continue to be made in unravelling the mysteries of the immunopathogenesis of fibrosing alveolitis in systemic sclerosis, and this should eventually lead to the development of more rational and targeted pharmacological therapies.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 1","pages":"Pages 10-14"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.09.016","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136554837","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
A 19–year–old man with severe obstructive lung disease 一名患有严重阻塞性肺病的19岁男子
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.09.009
Abubakr A. Bajwa, Faisal Usman , Danny Pulido , James D. Cury , Luis Laos
{"title":"A 19–year–old man with severe obstructive lung disease","authors":"Abubakr A. Bajwa,&nbsp;Faisal Usman ,&nbsp;Danny Pulido ,&nbsp;James D. Cury ,&nbsp;Luis Laos","doi":"10.1016/j.rmedc.2009.09.009","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.09.009","url":null,"abstract":"<div><p>A 19-year-old boy presented to ambulatory clinic with shortness of breath after walking two blocks. He denied any cough, orthopnea, chest pain or hemoptysis. Ten months prior to admission he was admitted to the medical intensive care unit with respiratory failure and was diagnosed with Goodpasture syndrome. He was treated with cyclophosphamide and steroids. He was discharged home after recovering. Patient subsequently developed dyspnea on minimal exertion. Spirometry showed severe obstructive lung disease and HRCT of chest showed diffuse micronodular disease with patchy ground-glass opacities, mild bronchiectasis and bronchiolectasis. Serologies for goodpasture syndrome were normal. A diagnosis of post-Goodpasture syndrome constrictive bronchiolitis was made. Due to severity of symptoms he was treated with azithromycin. His FEV1 doubled in 3 months and in addition to significant clinical improvement the HRCT findings also improved. This is the first described case of constrictive bronciolitis developing as an aftermath of Goodpasture syndrome.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 3","pages":"Pages 153-155"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.09.009","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91958503","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pharmacodynamics and tolerability of high-dose, prolonged infusion carbapenems in adults with cystic fibrosis – A review of 3 cases 3例成人囊性纤维化患者大剂量、长时间输注碳青霉烯类药物的药效学和耐受性
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.09.011
Catharine C. Bulik , Richard Quintiliani Jr. , J. Samuel Pope , Joseph L. Kuti , David P. Nicolau
{"title":"Pharmacodynamics and tolerability of high-dose, prolonged infusion carbapenems in adults with cystic fibrosis – A review of 3 cases","authors":"Catharine C. Bulik ,&nbsp;Richard Quintiliani Jr. ,&nbsp;J. Samuel Pope ,&nbsp;Joseph L. Kuti ,&nbsp;David P. Nicolau","doi":"10.1016/j.rmedc.2009.09.011","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.09.011","url":null,"abstract":"<div><p>Cystic fibrosis (CF) is a disease marked by repeated acute pulmonary exacerbations of infections, often caused by <em>Pseudomonas aeruginosa</em> and <em>Burkholderia cepacia</em>. As antibiotic susceptibility declines, dose optimization must be considered to provide adequate pharmacodynamic exposure. We report three cases of CF exacerbations in adults caused by multi-drug resistant <em>P. aeruginosa</em> and <em>B. cepacia.</em> Each case required dosing strategies greater than currently recognized in package inserts: meropenem 3000<!--> <!-->mg every 8<!--> <!-->h (3-hour infusion) and doripenem 2000<!--> <!-->mg every 8<!--> <!-->h (4-hour infusion). Pharmacokinetic analyses demonstrated that targeted pharmacodynamic exposures were achieved against most of the organisms, resulting in clinical improvements despite laboratory reported resistance. The high-dose, prolonged infusion regimens were well tolerated demonstrating that pharmacodynamically optimized carbapenem regimens may be used safely and effectively in patients with limited conventional treatment options.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 3","pages":"Pages 146-149"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.09.011","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91958507","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 19
Congenital lobar emphysema in adult: A rare case report 成人先天性肺气肿1例报告
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.09.010
M. Khalid, S. Saleemi, B. Khan
{"title":"Congenital lobar emphysema in adult: A rare case report","authors":"M. Khalid,&nbsp;S. Saleemi,&nbsp;B. Khan","doi":"10.1016/j.rmedc.2009.09.010","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.09.010","url":null,"abstract":"<div><p>Congenital lobar emphysema (CLE) is a very rare disease characterized by over-distension of the affected lobe leading to compression and displacement of adjacent normal lung tissue and mediastinum. We present a case of 18 years old male who presented with symptoms of acute bronchitis and routine chest X-ray led to the suspicion of CLE which was confirmed by advance imaging techniques. We reviewed the literature to discuss this very rare illness which almost always present in early years of life and only a handful cases are reported in adults.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 3","pages":"Pages 150-152"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.09.010","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91958508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
Diffuse alveolar hemorrhage with chronic thyroiditis in an advanced-age adult 弥漫性肺泡出血并发慢性甲状腺炎1例
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.04.006
Masanori Fujii, Nobuaki Miyahara, Yasushi Tanimoto, Nagio Takigawa, Masahiro Tabata, Arihiko Kanehiro, Katsuyuki Kiura, Mitsune Tanimoto
{"title":"Diffuse alveolar hemorrhage with chronic thyroiditis in an advanced-age adult","authors":"Masanori Fujii,&nbsp;Nobuaki Miyahara,&nbsp;Yasushi Tanimoto,&nbsp;Nagio Takigawa,&nbsp;Masahiro Tabata,&nbsp;Arihiko Kanehiro,&nbsp;Katsuyuki Kiura,&nbsp;Mitsune Tanimoto","doi":"10.1016/j.rmedc.2009.04.006","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.04.006","url":null,"abstract":"<div><p>Idiopathic pulmonary hemosiderosis (IPH) is one of the rare causes of diffuse alveolar hemorrhage (DAH), and usually occurs in children. The mechanism underlying this disease development has not been defined. During the acute phase, death due to massive alveolar hemorrhage and subsequent severe respiratory failure with multiple organ failure often occurs. We report a case of IPH which occurred in an advanced-aged adult during following thyroidectomy for chronic thyroiditis. Following surgery this 83-year-old male developed acute onset dyspnea and pulmonary hemorrhage. In a search for underlying causes, no disorders were found and the only finding was the presence of anti-thyroid antibody. Systemic corticosteroid therapy was effective and he fully recovered. To our knowledge, this is the second documentation of IPH in association with chronic thyroiditis.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 2","pages":"Pages 90-92"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.04.006","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137159019","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Squamous cell carcinoma of the lungs arising in recurrent respiratory papillomatosis 复发性呼吸道乳头状瘤病引起的肺部鳞状细胞癌
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.09.021
Dalia Hammoud, Boutros El Haddad
{"title":"Squamous cell carcinoma of the lungs arising in recurrent respiratory papillomatosis","authors":"Dalia Hammoud,&nbsp;Boutros El Haddad","doi":"10.1016/j.rmedc.2009.09.021","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.09.021","url":null,"abstract":"<div><p>Squamous papillomas of the lung are an uncommon feature of recurrent respiratory papillomatosis (RRP), occurring in fewer than 1% of cases. We describe an 18-year-old male patient with pulmonary papilloma who developed a fatal squamous cell carcinoma of the lung. Both benign papillomas and invasive carcinoma were positive for human papilloma virus subtype 6 and 11. These findings suggest that HPV 6 and 11 are correlated with malignant transformation in the setting of juvenile-onset recurrent respiratory papillomatosis even without tobacco or radiation exposure.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 4","pages":"Pages 270-272"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.09.021","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137088209","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
A case of cryptococcal pneumonia with false-positive [18F]fluoro-2-deoxy-d-glucose positron emission tomography (FDG-PET) image mimicking lung metastatic cancer 隐球菌性肺炎1例假阳性[18F]氟-2-脱氧-d-葡萄糖正电子发射断层扫描(FDG-PET)图像模拟肺转移癌
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.04.005
Cheng Ji , Chunhua Ling , Bin Zhang , Haodong Xu
{"title":"A case of cryptococcal pneumonia with false-positive [18F]fluoro-2-deoxy-d-glucose positron emission tomography (FDG-PET) image mimicking lung metastatic cancer","authors":"Cheng Ji ,&nbsp;Chunhua Ling ,&nbsp;Bin Zhang ,&nbsp;Haodong Xu","doi":"10.1016/j.rmedc.2009.04.005","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.04.005","url":null,"abstract":"<div><h3>Background</h3><p>There is an increasing use of positron emission tomography with [<sup>18</sup>F]fluoro-2-deoxy-<span>d</span>-glucose (FDG-PET) for differential diagnosis between lung malignancy and other pulmonary diseases such as infection. However, false-positive FDG-PET images mimicking lung cancer can occur in pulmonary infection.</p></div><div><h3>Objective</h3><p>This study was to describe a case of cryptococcal pneumonia with false-positive FDG-PET image mimicking metastatic lung cancer.</p></div><div><h3>Patient and results</h3><p>We analyzed the clinical features and chest CT and FDG-PET characteristics of a case of pulmonary cryptococcosis that was initially suspected to have lung metastasis of gastric cancer and treated by surgery. During a follow-up, the 49 years old, female patient with a 7-year history of gastric adenocarcinoma showed a 1.0-cm nodule in the right lower lobe of lung on her chest CT scan with an accumulation of FDG (SUV<!--> <!-->=<!--> <!-->4.5) on her PET image. With a clinical diagnosis of suspected lung metastatic cancer, the lung wedge resection was then performed. Histological analysis of the resected nodule confirmed a diagnosis of cryptococcal pneumonia.</p></div><div><h3>Conclusion</h3><p>The FDG-PET image is not particularly helpful in segregating pulmonary infection from lung malignancy in certain cases. Surgical resection is recommended for both diagnosis and treatment of pulmonary cryptococcosis.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 2","pages":"Pages 93-94"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.04.005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137159047","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lymphocytopenia-associated sarcoidosis: CD4+ T-cell hypo-responsiveness to IL-2 and lectin 淋巴细胞减少相关结节病:CD4+ t细胞对IL-2和凝集素的低反应性
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.04.001
Nathalie Freymond , Christophe Malcus , Yves Pacheco , Gilles Devouassoux
{"title":"Lymphocytopenia-associated sarcoidosis: CD4+ T-cell hypo-responsiveness to IL-2 and lectin","authors":"Nathalie Freymond ,&nbsp;Christophe Malcus ,&nbsp;Yves Pacheco ,&nbsp;Gilles Devouassoux","doi":"10.1016/j.rmedc.2009.04.001","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.04.001","url":null,"abstract":"<div><p>Despite classical identification of immune response impairment in sarcoidosis, such as anergy to delayed skin tests, the characterization of contributing mechanisms are still uncertain and infectious events complicating the course of the disease are unfrequent. Rarely, additional quantitative T-cell defects are reported in association with the disease. Although mechanisms of lymphocyte disorders are unknown, lymphocytopenia is usually revealed by an opportunistic infection.</p><p>We report the case of an 18-year-old man, with pulmonary sarcoidosis, treated by corticoids, who developed cryptococcal meningitis. A CD4+ T-cell defect was simultaneously discovered, which was not influenced by corticoid arrest, persisted following infection resolution and control of sarcoidosis. <em>In vitro</em> experiments were performed in parallel, demonstrating a restricted CD4+ T-cell proliferation hypo-responsiveness to both IL-2 and lectin. In addition, rhIL-2 subcutaneously administrated failed to restore peripheral T-cell count.</p><p>A multi-visceral sarcoidosis associated to CD4-lymphocytopenia is rarely reported and highly demonstrative of the related risk for an opportunistic infection development. In context, the absence of lectin and IL-2 effects on <em>in vitro</em> CD4+ T-cell proliferation assays and the inefficiency of <em>in vivo</em> rhIL-2 on T-cell count have been infrequently reported and suggested the presence of a defective intracellular signaling pathway, responsible for T cell defect.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 2","pages":"Pages 113-115"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.04.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137158511","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Bleeding diathesis due to vitamin K deficiency in an infant with cystic fibrosis 囊性纤维化婴儿维生素K缺乏引起的出血性素质
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.09.004
Antonia Popova , Jessica Foley , Samya Z. Nasr
{"title":"Bleeding diathesis due to vitamin K deficiency in an infant with cystic fibrosis","authors":"Antonia Popova ,&nbsp;Jessica Foley ,&nbsp;Samya Z. Nasr","doi":"10.1016/j.rmedc.2009.09.004","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.09.004","url":null,"abstract":"<div><p>With the wide implementation of newborn screening for Cystic Fibrosis, infants are being diagnosed in the presymptomatic phase of the disease. Nutritional deficiencies (hypoalbuminemia) and fat soluble vitamins A, D and E deficiencies, due to pancreatic insufficiency and malabsorption, have been reported in the past at the time of diagnosis.<span>1</span>, <span>2</span> Rarely, infants with CF present with severe bleeding disorder, secondary to vitamin K deficiency, in the first months of life.<span><sup>3</sup></span> To our knowledge, this is the first case report illustrating bleeding diathesis in a one month old infant with CF. He was diagnosed by newborn screening and presented with a gastrointestinal bleeding due to vitamin K deficient coagulopathy.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 3","pages":"Pages 165-166"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.09.004","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137350414","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Giant hydatid lung cysts: About two paediatric cases 巨大棘球蚴肺囊肿:约2例儿科病例
Respiratory medicine CME Pub Date : 2010-01-01 DOI: 10.1016/j.rmedc.2009.09.001
L. Ghedira Besbes , S. Haddad , Ch. Ben Meriem , S. Hammami , A. Nouri , M.N. Gueddiche
{"title":"Giant hydatid lung cysts: About two paediatric cases","authors":"L. Ghedira Besbes ,&nbsp;S. Haddad ,&nbsp;Ch. Ben Meriem ,&nbsp;S. Hammami ,&nbsp;A. Nouri ,&nbsp;M.N. Gueddiche","doi":"10.1016/j.rmedc.2009.09.001","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.09.001","url":null,"abstract":"<div><p>Cystic echinococcosis, which commonly starts during childhood or adolescence, is a serious problem of public health in Tunisia. The resulting large cysts in the lung are a special clinical entity called giant hydatid cysts. Herein we present two paediatric cases of this rare entity. In the first case a fourteen-year-old boy presented with chest pain, thoracic deformation, weight loss and dyspnea revealing two giant hydatid cysts of the upper and the lower lobes of the right lung. In the second case, a seven-year-old girl presented with chest pain, dyspnea, fever and episodes of suffocation revealing a giant hydatid cyst of the right upper lobe of the lung.</p><p>The three giant cysts were non-complicated, they were treated by cystotomy and capitonnage without post-operative complications and without recurrence of the disease on follow-up.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 3","pages":"Pages 174-178"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.09.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137350417","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
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