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
A Rare Association: Hereditary Hemorrhagic Telangiectasia with Liver Cirrhosis Causing Portal Hypertension. 罕见的关联：遗传性出血性远端血管扩张症与肝硬化导致的门静脉高压症。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2024-01-17 eCollection Date: 2024-01-01 DOI: 10.1155/2024/3574725
Denisse Morales-Tovar, Froylan D Martínez-Sánchez, Alejandro Gabutti-Thomas, Rodolfo Rivera-Martínez, Jacqueline Córdova-Gallardo
{"title":"A Rare Association: Hereditary Hemorrhagic Telangiectasia with Liver Cirrhosis Causing Portal Hypertension.","authors":"Denisse Morales-Tovar, Froylan D Martínez-Sánchez, Alejandro Gabutti-Thomas, Rodolfo Rivera-Martínez, Jacqueline Córdova-Gallardo","doi":"10.1155/2024/3574725","DOIUrl":"10.1155/2024/3574725","url":null,"abstract":"<p><p>Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is a vascular disorder of autosomal dominant etiology. The hallmark clinical feature is the presence of recurrent episodes of epistaxis in patients with vascular malformations and a tendency to bleed. We present the case of a 71-year-old woman who presented to the emergency department with upper gastrointestinal bleeding caused by esophageal varices, in conjunction with gastric angiodysplasias. The presence of oronasopharyngeal telangiectasias and hepatomegaly raised suspicion of HHT. The diagnostic workup confirmed the presence of angiodysplasia in the gastric region, portal arteriovenous malformation, and a pulmonary shunt.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2024 ","pages":"3574725"},"PeriodicalIF":0.6,"publicationDate":"2024-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10807975/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139565093","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
Refractory Cytomegalovirus Colitis in Common Variable Immunodeficiency Requiring Total Colectomy 需要进行全结肠切除术的常见变异性免疫缺陷症患者的难治性巨细胞病毒性结肠炎
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-12-21 DOI: 10.1155/2023/8888429
Sulaiman Almushir, Faisal Aljohani, A. Qatomah
{"title":"Refractory Cytomegalovirus Colitis in Common Variable Immunodeficiency Requiring Total Colectomy","authors":"Sulaiman Almushir, Faisal Aljohani, A. Qatomah","doi":"10.1155/2023/8888429","DOIUrl":"https://doi.org/10.1155/2023/8888429","url":null,"abstract":"Cytomegalovirus (CMV) colitis is an uncommon infection in immunocompetent hosts, usually occurring in the presence of an underlying immunodeficiency condition that allows for the reactivation of latent CMV infection. CMV colitis typically presents with persistent diarrhea, sometimes accompanied by bloody stools and nonspecific abdominal pain. We present the case of a 76-year-old woman known to have chronic CMV colitis, which was diagnosed in the context of underlying common variable immunodeficiency (CVID). Despite multiple attempts at managing CMV colitis, her symptoms persisted over the years. Ultimately, the patient required a pan colectomy due to refractory CMV colitis.","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"31 5","pages":""},"PeriodicalIF":0.7,"publicationDate":"2023-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138948548","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Case Report and Literature Review of a Rare Jejunal Solitary Peutz–Jeghers-Type Polyp Resected Endoscopically in an Elderly Patient Presenting with Subacute Gastrointestinal Bleeding 一名出现亚急性胃肠道出血的老年患者在内镜下切除了一个罕见的空肠孤立性 Peutz-Jeghers 型息肉的病例报告和文献综述
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-12-18 DOI: 10.1155/2023/2391602
Talal Alenezi, Victoria Marcus, T. Bessissow
{"title":"A Case Report and Literature Review of a Rare Jejunal Solitary Peutz–Jeghers-Type Polyp Resected Endoscopically in an Elderly Patient Presenting with Subacute Gastrointestinal Bleeding","authors":"Talal Alenezi, Victoria Marcus, T. Bessissow","doi":"10.1155/2023/2391602","DOIUrl":"https://doi.org/10.1155/2023/2391602","url":null,"abstract":"Solitary Peutz–Jeghers-type polyp (SPJP) is a rare hamartomatous lesion. It is considered a different entity from Peutz–Jeghers syndrome despite similar histopathological findings. It can be found in the GI tract but rarely in the jejunum. Jejunal SPJP is susceptible to necrosis, ulceration, and intussusception, resulting in GI bleeding or small bowel obstruction. We describe a case of subacute gastrointestinal bleeding secondary to jejunal SPJP to share our approach to this challenging case using therapeutic endoscopy. An 81-year-old male patient with a history of atrial fibrillation on warfarin with stable therapeutic INR levels presented with a 1-week history of melena, generalized fatigue, and shortness of breath on exertion and was found to have profound iron deficiency anemia. Esophageal gastroduodenoscopy and colonoscopy failed to identify the source of bleeding; however, single-balloon enteroscopy detected a 4 cm polyp with a stalk in the proximal jejunum. Endoscopic polypectomy was performed, and the whole polyp was removed. Histopathological examination was consistent with Peutz–Jeghers polyp. The genetic analysis was negative for STK11 mutation. Follow-up magnetic resonance enterography and video capsule endoscopy did not reveal any other polypoid lesion in the GI tract. The patient’s symptoms resolved gradually, and his hemoglobin level returned back to normal levels within 6 months. To our knowledge, this is the first case of endoscopic polypectomy during balloon-assisted enteroscopy for jejunal SPJP.","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"52 s180","pages":""},"PeriodicalIF":0.7,"publicationDate":"2023-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138995338","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dermatofibrosarcoma Protuberans (DFSP) with Fibrosarcomatous Changes in a Patient with Crohn's Disease Treated with Anti-TNF (Adalimumab). 抗肿瘤坏死因子（阿达木单抗）治疗克罗恩病患者的隆突皮肤纤维肉瘤（DFSP）伴纤维肉瘤改变。
IF 0.6
Case Reports in Gastrointestinal Medicine Pub Date : 2023-10-10 eCollection Date: 2023-01-01 DOI: 10.1155/2023/1057247
Ivo Klarin
{"title":"Dermatofibrosarcoma Protuberans (DFSP) with Fibrosarcomatous Changes in a Patient with Crohn's Disease Treated with Anti-TNF (Adalimumab).","authors":"Ivo Klarin","doi":"10.1155/2023/1057247","DOIUrl":"10.1155/2023/1057247","url":null,"abstract":"<p><p>Dermatofibrosarcoma protuberans (DFSP) is a low-to-intermediate grade sarcoma with a reported incidence of 4.1 per million person-years. Despite its local invasiveness, it rarely metastasizes (5% of cases). Fibrosarcomatous change in DFSP is a form of tumor progression that carries an increased risk of metastases. We reported a case of 45-year-old patient treated with adalimumab lasting 7 years for Crohn's disease who developed dermatofibrosarcoma protuberans with fibromatous changes. Adalimumab therapy was stopped before surgery, and ustekinumab was introduced 6 months after.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"1057247"},"PeriodicalIF":0.6,"publicationDate":"2023-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581855/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49683381","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
Transient Intussusception Mimicking Acute Coronary Syndrome. 模拟急性冠状动脉综合征的短暂性肠套叠。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-10-09 eCollection Date: 2023-01-01 DOI: 10.1155/2023/7324188
Hiroshi Imamura, Yuichiro Kashima, Yujiro Hamano, Aoi Ogawara
{"title":"Transient Intussusception Mimicking Acute Coronary Syndrome.","authors":"Hiroshi Imamura,&nbsp;Yuichiro Kashima,&nbsp;Yujiro Hamano,&nbsp;Aoi Ogawara","doi":"10.1155/2023/7324188","DOIUrl":"10.1155/2023/7324188","url":null,"abstract":"<p><p>Intussusception in adults is rare and usually associated with organic lesions. However, in the current era of computed tomography (CT), cases of idiopathic and transient intussusceptions are being increasingly diagnosed. Herein, we present a case of ileocecal intussusception with symptoms mimicking those of acute coronary syndrome. A male patient in his 80s with a history of myocardial infarction presented to the emergency department with acute onset of severe precordial and epigastric pain, cold sweating, and vomiting. Coronary angiography did not reveal any significant new lesion, while abdominal CT revealed ileocecal intussusception without bowel obstruction. The pain spontaneously subsided without any intervention, and the patient was discharged on the sixth hospital day. Cases of intussusception may go unnoticed in patients suspected of having chest pain with a normal coronary arteriogram, as idiopathic intussusception is relatively common and subsides spontaneously. Therefore, physicians should note that intussusception is one of the differential diagnoses of acute coronary syndrome.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"7324188"},"PeriodicalIF":0.7,"publicationDate":"2023-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578975/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41239730","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
Aeromonas caviae-Associated Severe Bloody Diarrhea. 豚鼠气单胞菌相关性严重血液性腹泻。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-10-09 eCollection Date: 2023-01-01 DOI: 10.1155/2023/4966879
Xiaolan Tang, Anuoluwa Oyetoran, Tyler Jones, Christopher Bray
{"title":"<i>Aeromonas caviae</i>-Associated Severe Bloody Diarrhea.","authors":"Xiaolan Tang,&nbsp;Anuoluwa Oyetoran,&nbsp;Tyler Jones,&nbsp;Christopher Bray","doi":"10.1155/2023/4966879","DOIUrl":"10.1155/2023/4966879","url":null,"abstract":"<p><p><i>Aeromonas</i> species are capable of inducing severe infections in both immunocompetent and immunocompromised individuals. Gastroenteritis is the most common infection associated with <i>Aeromonas</i> species in humans. We report a rare case of <i>Aeromonas caviae</i> severe gastroenteritis and bloody diarrhea that led to the development of sepsis in a 45-year-old female with no history of immunocompromising conditions. This patient required extensive medical support which included blood transfusions and antibiotics. Fortunately, with appropriate diagnostic measures and targeted antibiotic therapy, her symptoms resolved. <i>Aeromonas</i> species are becoming increasingly frequent among the pathogens isolated from patients suffering from gastroenteritis. As such, it is becoming increasingly important for clinicians to consider this pathogen when working up their patients for diarrhea.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"4966879"},"PeriodicalIF":0.7,"publicationDate":"2023-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10578977/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41239729","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
Severe Gastrointestinal Hemorrhage due to Monkeypox Virus-Associated Proctocolitis. 猴痘病毒相关性直结肠炎致严重胃肠道出血。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9981631
Sobaan Taj, Chris Austin, Azhar Hussain, Maryam Salma Babar, Harshavardhan Sanekommu, Steven Imburgio, Anmol Johal, Alejandro CruzPonce, Apurva Vedire, Edward Liu
{"title":"Severe Gastrointestinal Hemorrhage due to Monkeypox Virus-Associated Proctocolitis.","authors":"Sobaan Taj,&nbsp;Chris Austin,&nbsp;Azhar Hussain,&nbsp;Maryam Salma Babar,&nbsp;Harshavardhan Sanekommu,&nbsp;Steven Imburgio,&nbsp;Anmol Johal,&nbsp;Alejandro CruzPonce,&nbsp;Apurva Vedire,&nbsp;Edward Liu","doi":"10.1155/2023/9981631","DOIUrl":"https://doi.org/10.1155/2023/9981631","url":null,"abstract":"<p><p>Monkeypox is primarily a painful cutaneous disease with occasional systemic manifestations. Monkeypox is transmitted predominantly through close physical contact and occasionally sexual contact. The first case was reported in the United States on May 17, 2022, in a recent monkeypox worldwide outbreak. We present a case of severe gastrointestinal bleeding as an atypical manifestation of monkeypox infection in a 40-year-old male with HIV. In our case, monkeypox-induced proctocolitis progressed to severe rectal bleeding requiring one unit of packed red blood cells transfusion despite one week of tecovirimat (TPOXX) therapy. So, patients should be educated about the possibility of unusual complications of monkeypox infection, i.e., bleeding in immunocompromised hosts.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"9981631"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10365909/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10233485","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
Gastrointestinal Stromal Tumours (GISTs) with KRAS Mutation: A Rare but Important Subset of GISTs. 伴有KRAS突变的胃肠道间质瘤(gist):一种罕见但重要的胃肠道间质瘤子集。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/4248128
Dorinda Mullen, Rajkumar Vajpeyi, Jose-Mario Capo-Chichi, Klaudia Nowak, Newton Wong, Runjan Chetty
{"title":"Gastrointestinal Stromal Tumours (GISTs) with KRAS Mutation: A Rare but Important Subset of GISTs.","authors":"Dorinda Mullen,&nbsp;Rajkumar Vajpeyi,&nbsp;Jose-Mario Capo-Chichi,&nbsp;Klaudia Nowak,&nbsp;Newton Wong,&nbsp;Runjan Chetty","doi":"10.1155/2023/4248128","DOIUrl":"https://doi.org/10.1155/2023/4248128","url":null,"abstract":"<p><p>Gastrointestinal stromal tumours (GISTs) are the most common mesenchymal tumours of the GI tract, usually found in the stomach, jejunum, and ileum. Typically, they are <i>KIT</i> or <i>PDGFR</i>-mutated, allowing for targetable treatments with tyrosine kinase inhibitors such as imatinib. Here, we present two <i>KRAS</i>-mutated wild-type gastrointestinal tumours (GISTs). Both cases occurred in the small bowel of females. Immunohistochemical studies on both tumours showed KIT and DOG-1 positivity, with SDHB retained. Molecular analysis revealed a <i>KRAS G12D</i> mutation and a <i>KRAS G13D</i> mutation, respectively. Wild-type GISTs are extremely uncommon. They typically occur in the stomach or the small bowel. <i>KRAS</i> is one of the genes implicated in this subset of GIST, with <i>KRAS G12D</i> being the most frequently encountered mutation. GIST <i>KRAS</i> mutations can arise alone or in conjunction with <i>KIT, PDFRA</i>, or <i>BRAF</i> mutations. Identification of these rare molecular subtypes is clinically important due to their resistance to imatinib therapy.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"4248128"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10471449/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10153240","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 Crohn's Disease Patient Found to Have Entamoeba histolytica Infection Causing Pyogenic Liver Abscess. 克罗恩病患者发现有溶组织内阿米巴感染导致化脓性肝脓肿。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9936613
Hannah Saven, Ashton Harmacinski, Andrew Canakis, Uni Wong
{"title":"A Crohn's Disease Patient Found to Have <i>Entamoeba histolytica</i> Infection Causing Pyogenic Liver Abscess.","authors":"Hannah Saven,&nbsp;Ashton Harmacinski,&nbsp;Andrew Canakis,&nbsp;Uni Wong","doi":"10.1155/2023/9936613","DOIUrl":"https://doi.org/10.1155/2023/9936613","url":null,"abstract":"<p><p><i>Entamoeba histolytica</i> is a parasite that typically causes amoebic dysentery but can result in complications such as pyogenic liver abscess. Patients with inflammatory bowel disease often take immunosuppressive therapies that make them more susceptible to such infections. Notably, parasitic infections in this context are rare in nonendemic areas. We describe a 57-year-old man who recently started infliximab therapy for Crohn's disease and presented with fever and right upper quadrant pain. While hospitalized, this patient was diagnosed with <i>Entamoeba histolytica</i> liver abscess. This case demonstrates that parasitic infections should be considered early in immunocompromised patients with inflammatory bowel disease.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"9936613"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10406523/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9968635","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
Necrotizing Pancreatitis Infected with Stenotrophomonas maltophilia: An Emerging Rare Multidrug-Resistant Organism. 坏死性胰腺炎感染嗜麦芽窄养单胞菌:一种新兴的罕见多重耐药生物。
IF 0.7
Case Reports in Gastrointestinal Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/8071158
Sophia Dar, Nooraldin Merza, Maryam Haider, Yousaf Zafar, Noren Din, Rosario Ligresti, Rani Sebti
{"title":"Necrotizing Pancreatitis Infected with <i>Stenotrophomonas maltophilia</i>: An Emerging Rare Multidrug-Resistant Organism.","authors":"Sophia Dar,&nbsp;Nooraldin Merza,&nbsp;Maryam Haider,&nbsp;Yousaf Zafar,&nbsp;Noren Din,&nbsp;Rosario Ligresti,&nbsp;Rani Sebti","doi":"10.1155/2023/8071158","DOIUrl":"https://doi.org/10.1155/2023/8071158","url":null,"abstract":"<p><p><i>Stenotrophomonas maltophilia</i> (SM) is a multidrug-resistant, Gram-negative (GN) bacillus that is an increasingly recognized nosocomial and environment pathogen. It is intrinsically resistant to carbapenems, a drug commonly utilized in the management of necrotizing pancreatitis (NP). We report a 21-year-old immunocompetent female with NP complicated by pancreatic fluid collection (PFC) infected with SM. One-third of patients with NP will develop infections by GN bacteria, while broad-spectrum antibiotics, including carbapenems, cover most infections, trimethoprim-sulfamethoxazole (TMP-SMX) is the first-line treatment antibiotic for SM. This case is critical because it highlights a rare pathogen that should be considered a causal pathogen in patients who do not respond to their care plan.</p>","PeriodicalId":45645,"journal":{"name":"Case Reports in Gastrointestinal Medicine","volume":"2023 ","pages":"8071158"},"PeriodicalIF":0.7,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10313464/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9801313","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
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