发布求助
文献互助 智能选刊 最新文献

Case Reports in Gastrointestinal Medicine最新文献

筛选
英文 中文
McKittrick-Wheelock Syndrome: A Rare Case of Secretory Diarrhea. McKittrick-Wheelock综合征:罕见的分泌性腹泻病例。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2022-01-01 DOI: 10.1155/2022/2097364
Mohammad Nabil Rayad, Noreen Mirza, Maria Bernardeth Herrera-Gonzalez, Yatinder Bains, Sarahi Herrera-Gonzalez
{"title":"McKittrick-Wheelock Syndrome: A Rare Case of Secretory Diarrhea.","authors":"Mohammad Nabil Rayad,&nbsp;Noreen Mirza,&nbsp;Maria Bernardeth Herrera-Gonzalez,&nbsp;Yatinder Bains,&nbsp;Sarahi Herrera-Gonzalez","doi":"10.1155/2022/2097364","DOIUrl":"https://doi.org/10.1155/2022/2097364","url":null,"abstract":"<p><p>McKittrick-Wheelock syndrome commonly presents with a triad of chronic secretory diarrhea, electrolyte disturbances, and renal failure. Secretory diarrhea is due to active ion secretion secondary to secretagogue secretion (cyclic adenosine monophosphate and prostaglandin E2). The mainstay of treatment for these lesions is surgical since it will arrest the loss of electrolytes that may lead to serious clinical consequences. Nonsteroidal anti-inflammatory drugs (NSAIDs) such as indomethacin may be used to decrease electrolyte secretion in patients that desire a nonsurgical approach. Our patient is unique in that this is the first case of a tubular adenoma with high-grade dysplasia leading to MWS and progressing to circulatory collapse with severe electrolyte disturbances. Aggressive replacement of fluids and electrolytes is essential to the survival of these patients.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2022 ","pages":"2097364"},"PeriodicalIF":0.7,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9744606/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10354477","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: 1
A Rare Case of Pseudomembranous Colitis Presenting with Pleural Effusion and Ascites with Literature Review. 假膜性结肠炎以胸腔积液及腹水表现一例并附文献复习。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-12-31 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6019068
Hossain Salehi, Amir Mohammad Salehi
{"title":"A Rare Case of Pseudomembranous Colitis Presenting with Pleural Effusion and Ascites with Literature Review.","authors":"Hossain Salehi,&nbsp;Amir Mohammad Salehi","doi":"10.1155/2021/6019068","DOIUrl":"https://doi.org/10.1155/2021/6019068","url":null,"abstract":"<p><p><i>Clostridium difficile</i> infection usually results from long-term and irregular antibiotic intake. The high-risk individuals for this infection include the patients undergoing chemotherapy due to malignancy, immunocompromised patients, and hospitalized patients receiving broad-spectrum antibiotics. The most common clinical manifestation of <i>Clostridium difficile</i> infection is diarrhea. However, pleural effusion and ascites have rarely been observed. As mentioned, these manifestations can be developed in a patient being treated with broad-spectrum antibiotics. Therefore, the present study reports a rare case of <i>Clostridium difficile</i> infection manifesting with these rare manifestations who was a 78-year-old female patient with a history of COVID-19, orthopedic surgery, and antibiotic treatment with cefixime and gentamicin.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"6019068"},"PeriodicalIF":0.7,"publicationDate":"2021-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741396/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39802850","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
Hepatitis B-Associated Symptomatic Iron Overload, with Complete Resolution after Nucleoside Analogue Treatment. 乙型肝炎相关的症状性铁超载，核苷类似物治疗后完全解决。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-12-27 eCollection Date: 2021-01-01 DOI: 10.1155/2021/8407257
Tze Tong Tey, Richard Yiu, Wei Qiang Leow
{"title":"Hepatitis B-Associated Symptomatic Iron Overload, with Complete Resolution after Nucleoside Analogue Treatment.","authors":"Tze Tong Tey,&nbsp;Richard Yiu,&nbsp;Wei Qiang Leow","doi":"10.1155/2021/8407257","DOIUrl":"https://doi.org/10.1155/2021/8407257","url":null,"abstract":"<p><p>Symptomatic iron overload and hyperferritinemia are rarely mentioned as complications of chronic hepatitis B infection. We report a case of a 70-year-old woman who presented with symptoms of iron overload including aches in the calves, fatigue, poor appetite, and low mood. Laboratory results showed a serum ferritin of 2449 <i>μ</i>g/L and transferrin saturation of 74%. Her symptoms completely resolved with hepatitis B antiviral treatment. Serum ferritin and transferrin saturation also normalized. Symptomatic iron overload is a rare yet clinically important complication that can result from chronic hepatitis B infection.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"8407257"},"PeriodicalIF":0.7,"publicationDate":"2021-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8723841/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39788033","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
Ileocaecal Tuberculosis Presenting with Massive Hematochezia: A Rare Clinical Manifestation. 以大量便血为表现的回盲肠结核:一种罕见的临床表现。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-12-10 eCollection Date: 2021-01-01 DOI: 10.1155/2021/1161135
Neha Mehta, Man Bahadur Paudyal, Sangam Shah, Rajan Chamlagain, Moon Shrestha, Ashish Mehta, Prabin Bhattarai
{"title":"Ileocaecal Tuberculosis Presenting with Massive Hematochezia: A Rare Clinical Manifestation.","authors":"Neha Mehta,&nbsp;Man Bahadur Paudyal,&nbsp;Sangam Shah,&nbsp;Rajan Chamlagain,&nbsp;Moon Shrestha,&nbsp;Ashish Mehta,&nbsp;Prabin Bhattarai","doi":"10.1155/2021/1161135","DOIUrl":"https://doi.org/10.1155/2021/1161135","url":null,"abstract":"<p><p>Abdominal pain, diarrhea, weight loss, anorexia, and fever are common symptoms of intestinal tuberculosis, while bleeding from the lumen, intestinal obstruction, perforation, and fistula formation are uncommon presentations in ileocaecal tuberculosis. Here, we present a case of a 33-year-old male with intestinal tuberculosis who initially presented with massive bleeding per rectum.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"1161135"},"PeriodicalIF":0.7,"publicationDate":"2021-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8683165/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39827973","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
Bleeding Meckel's Diverticulum in a 33-Year-Old Female Diagnosed with Video Capsule Endoscopy and a Technetium-99 m Pertechnetate Scan with a Favorable Response to H2 Blocker and PPI. 33岁女性梅克尔憩室出血患者，经视频胶囊内窥镜和锝-99米高锝酸盐扫描诊断，H2阻滞剂和PPI反应良好。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-12-09 eCollection Date: 2021-01-01 DOI: 10.1155/2021/1381395
Gregor Krstevski, Urim Isahi, Vladimir Andreevski
{"title":"Bleeding Meckel's Diverticulum in a 33-Year-Old Female Diagnosed with Video Capsule Endoscopy and a Technetium-99 m Pertechnetate Scan with a Favorable Response to H<sub>2</sub> Blocker and PPI.","authors":"Gregor Krstevski,&nbsp;Urim Isahi,&nbsp;Vladimir Andreevski","doi":"10.1155/2021/1381395","DOIUrl":"https://doi.org/10.1155/2021/1381395","url":null,"abstract":"<p><p>Meckel's diverticulum is a true diverticulum consisting of all three layers of the small intestine resulting from incomplete regression of the vitelline duct. While it is often benign, it can present with serious complications such as intussusception, ulceration, torsion, hemorrhage, obstruction, inflammation, and fistula formation. Although it typically presents in infancy and early childhood, it can also manifest much later into adulthood. We report a case of Meckel's diverticulum complicated by significant bleeding in a 33-year-old female patient. Diagnosis was accomplished with video capsule endoscopy and a technetium-99 m pertechnetate scan. The patient responded well to acid suppression, initially with an H<sub>2</sub> blocker and later with a PPI (proton pump inhibitor), and remained asymptomatic for nearly four months in the interim to definitive surgical treatment. Microscopic examination of the resected diverticulum confirmed the presence of ectopic gastric mucosa. A PubMed literature search revealed several similar cases of Meckel's diverticulum complicated by hemorrhage with a favorable response to H<sub>2</sub> blockers and PPIs. While surgical resection remains the mainstay of definitive treatment, medications aimed at acid suppression can delay the need for urgent surgery, allow for diagnostic assessment, and optimize conditions for elective surgical treatment.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"1381395"},"PeriodicalIF":0.7,"publicationDate":"2021-12-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8677379/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39827974","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
Gastric Signet-Ring Cell Carcinoma That Presented as an Elevated Lesion due to Fibromuscular Obliteration in the Lamina Propria. 胃印戒细胞癌因固有层纤维肌闭塞而表现为升高的病变。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-11-24 eCollection Date: 2021-01-01 DOI: 10.1155/2021/2887256
Yoshitsugu Misumi, Shin Ichihara, Kouichi Nonaka, Hiromi Onizuka, Yoji Nagashima
{"title":"Gastric Signet-Ring Cell Carcinoma That Presented as an Elevated Lesion due to Fibromuscular Obliteration in the Lamina Propria.","authors":"Yoshitsugu Misumi,&nbsp;Shin Ichihara,&nbsp;Kouichi Nonaka,&nbsp;Hiromi Onizuka,&nbsp;Yoji Nagashima","doi":"10.1155/2021/2887256","DOIUrl":"https://doi.org/10.1155/2021/2887256","url":null,"abstract":"<p><p>The widespread use of <i>Helicobacter pylori</i> eradication therapy in recent years has reduced the <i>H. pylori</i> infection rate, indicating that gastric cancer cases diagnosed in the future may be <i>H. pylori</i>-naïve. The typical endoscopic presentation of signet-ring cell carcinoma, which accounts for the majority of <i>H. pylori-</i>naïve gastric cancer cases, is a discolored, flat, or depressed lesion; it is rarely presented as an elevated lesion. In this study, we treated a patient with elevated signet-ring cell carcinoma in an <i>H. pylori-</i>naïve stomach. Histopathological testing after endoscopic submucosal dissection showed proliferation of fibromuscular tissue in the tumor, which may have caused the formation of the elevated lesion.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"2887256"},"PeriodicalIF":0.7,"publicationDate":"2021-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8635901/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39572471","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: 1
An Alarming Mimicry of Intra-Abdominal Infections: Acute Appendiceal Diverticulitis. 腹腔内感染的惊人模拟:急性阑尾憩室炎。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-11-12 eCollection Date: 2021-01-01 DOI: 10.1155/2021/6131015
Youseung Kim, Varun Kesar, Douglas Grider, Maithili V Chitnavis
{"title":"An Alarming Mimicry of Intra-Abdominal Infections: Acute Appendiceal Diverticulitis.","authors":"Youseung Kim,&nbsp;Varun Kesar,&nbsp;Douglas Grider,&nbsp;Maithili V Chitnavis","doi":"10.1155/2021/6131015","DOIUrl":"https://doi.org/10.1155/2021/6131015","url":null,"abstract":"<p><p>A 65-year-old woman presented with three days of colicky abdominal pain. Abdominal imaging illustrated small bowel enteritis, ascites in both paracolic gutters, and incidental hepatic steatosis. Although ascites fluid demonstrated high neutrophil count consistent with peritonitis and the patient received adequate antibiotics, she clinically deteriorated. Subsequent exploratory laparotomy revealed necrotic appendix and multiple intra-abdominal abscesses. Histopathology showed acute suppurative appendicitis with multiple other intact small diverticula, indicating likely perforation of inflamed appendiceal diverticula with subsequent abscess formation and abdominal peritonitis. This case highlights the importance of ascites fluid analysis and continued clinical correlation, especially in cases of rare entities with atypical presentations.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"6131015"},"PeriodicalIF":0.7,"publicationDate":"2021-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604594/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39897526","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
Acute Mesenteric Ischemia in a COVID-19 Patient: Delay in Referral and Recommendation for Surgery. 1例COVID-19患者急性肠系膜缺血:延迟转诊和推荐手术
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-11-12 eCollection Date: 2021-01-01 DOI: 10.1155/2021/1999931
Mohammad Hossein Bagheripour, Mohammad Ali Zakeri
{"title":"Acute Mesenteric Ischemia in a COVID-19 Patient: Delay in Referral and Recommendation for Surgery.","authors":"Mohammad Hossein Bagheripour,&nbsp;Mohammad Ali Zakeri","doi":"10.1155/2021/1999931","DOIUrl":"10.1155/2021/1999931","url":null,"abstract":"<p><p>Coronavirus (COVID-19) is more common with symptoms such as fever, dry cough, and shortness of breath. However, it may be associated with COVID-19-induced gastrointestinal (GI) symptoms including acute mesenteric ischemia (AMI). These conditions make the diagnosis of AMI challenging. Timely referral with correct diagnosis and attention to the uncommon symptoms of COVID-19 can play an important role in the management and treatment of AMI in COVID-19 patients. We present a patient with AMI due to thrombotic complications of COVID-19, who referred to the hospital too late and ignored the recommendation for abdominal surgery.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"1999931"},"PeriodicalIF":0.7,"publicationDate":"2021-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8589525/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39877297","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
CMV-Related Gastric Ulcer and Gastroduodenitis in an Immunocompetent Patient: A Case Report and Literature Review. 免疫正常患者巨细胞病毒相关胃溃疡和胃十二指肠炎1例报告及文献复习。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-11-12 eCollection Date: 2021-01-01 DOI: 10.1155/2021/3513223
Andrawus Beany, Tova Rainis
{"title":"CMV-Related Gastric Ulcer and Gastroduodenitis in an Immunocompetent Patient: A Case Report and Literature Review.","authors":"Andrawus Beany,&nbsp;Tova Rainis","doi":"10.1155/2021/3513223","DOIUrl":"https://doi.org/10.1155/2021/3513223","url":null,"abstract":"<p><strong>Background: </strong>Cytomegalovirus (CMV)- related gastroduodenal infection is rare in immunocompetent hosts, and although it is considered a self-limiting condition in most cases, there is scarce literature to assert its management. <i>Case Presentation</i>. We report a case of a 66-year-old immunocompetent male patient diagnosed with a giant gastric ulcer caused by CMV infection. The ulcer manifested as refractory vomiting and melena. Rapid and full resolution was observed on proton-pump inhibitor (PPI) monotherapy.</p><p><strong>Conclusion: </strong>Gastric CMV infection might mimic an advanced gastric tumor in individuals with an intact immune system. The condition is rare, and the diagnosis is challenging and oftentimes overlooked. However, a rapid resolution has been documented in all cases, even without antiviral therapy.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"3513223"},"PeriodicalIF":0.7,"publicationDate":"2021-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604585/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39897527","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 Novel Cause of Biliary Peritonitis after Endoscopic Retrograde Cholangiopancreatography: Case Report and Literature Review. 内镜逆行胆管造影后胆性腹膜炎的新病因:病例报告及文献复习。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2021-10-21 eCollection Date: 2021-01-01 DOI: 10.1155/2021/3814080
Andrija Karačić, Paula Batur, Domagoj Štritof, Taro Fukui, Branko Bakula, Inka Kekez
{"title":"A Novel Cause of Biliary Peritonitis after Endoscopic Retrograde Cholangiopancreatography: Case Report and Literature Review.","authors":"Andrija Karačić,&nbsp;Paula Batur,&nbsp;Domagoj Štritof,&nbsp;Taro Fukui,&nbsp;Branko Bakula,&nbsp;Inka Kekez","doi":"10.1155/2021/3814080","DOIUrl":"https://doi.org/10.1155/2021/3814080","url":null,"abstract":"<p><strong>Background: </strong>Endoscopic retrograde cholangiopancreatography (ERCP) can lead to several complications such as duodenal or bile duct perforation. The incidence of pneumoperitoneum post-ERCP is rarely seen (<1%) and is associated with perforations of the duodenum or common bile duct in therapeutic ERCP after sphincterotomy. In this case, we disclose a novel cause of biliary peritonitis after ERCP. <i>Case Presentation</i>. A 65-year-old man presented with abdominal pain and distended abdomen after uneventful ERCP with sphincterotomy. An abdominal computed tomography (CT) was performed whose finding indicated duodenal perforation. The patient was rushed to an emergency laparotomy where only a rupture of an otherwise normal subcapsular intrahepatic bile duct was found. The surrounding liver parenchyma was healthy. The cause of this condition was probably post-ERCP pneumobilia and the increase of pressure in the biliary tract.</p><p><strong>Conclusions: </strong>This is the first case in literature describing the rupture of a subcapsular healthy bile duct as cause of biliary peritonitis after ERCP. This case also suggests that in the management of post-ERCP complications, the cooperation of radiologists and surgeons is vital for the patient's wellbeing.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2021 ","pages":"3814080"},"PeriodicalIF":0.7,"publicationDate":"2021-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8553500/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39580275","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
首页 上一页 下一页 尾页
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
现在去查看 取消
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
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