Journal of Aapos最新文献

筛选
英文 中文
Increase in blood derived mitochondrial DNA copy number in strabismus patients. 斜视患者血液中线粒体 DNA 拷贝数的增加。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-12-01 Epub Date: 2024-11-13 DOI: 10.1016/j.jaapos.2024.104042
Zainab Zehra, Muhammad Amn Zia, Sorath Noorani Siddiqui, Christopher S von Bartheld, Maleeha Azam, Raheel Qamar
{"title":"Increase in blood derived mitochondrial DNA copy number in strabismus patients.","authors":"Zainab Zehra, Muhammad Amn Zia, Sorath Noorani Siddiqui, Christopher S von Bartheld, Maleeha Azam, Raheel Qamar","doi":"10.1016/j.jaapos.2024.104042","DOIUrl":"10.1016/j.jaapos.2024.104042","url":null,"abstract":"<p><strong>Background: </strong>Abnormalities in mitochondrial energy homeostasis can lead to various disorders, including ocular motility aberrations. Previous studies have suggested the involvement of mitochondrial aberrations in strabismus etiology. We compared the blood-derived mitochondrial DNA (mtDNA) copy number from comitant strabismus patients with that from age-matched controls, and also compared expression of mitochondrial biogenesis genes in a separate set of extraocular muscle samples from strabismic and control subjects.</p><p><strong>Methods: </strong>Blood samples from 93 strabismic (39 esotropic, 54 exotropic) and 93 control subjects were analyzed for mtDNA copy number through quantitative polymerase chain reaction. We also examined the expression of 6 genes involved in mitochondrial biogenesis in cDNA obtained from extraocular muscles of a separate group of 26 strabismus patients and 4 healthy controls.</p><p><strong>Results: </strong>The mtDNA content was significantly higher in strabismus patients as compared to the control group, both overall (fold change, 1.39; Z = -2.43 [P = 0.01]) and in strabismus subgroups (esotropia: fold change,1.42; Z = 2.59 [P = 0.0096]; exotropia: fold change, 1.41, Z = 3.35 [P = 0.00078]). No significant difference was observed in the expression of the examined biogenesis genes between strabismus and control groups.</p><p><strong>Conclusions: </strong>Our results suggest an association between mtDNA copy number and strabismus; however, further studies are required to elucidate the significance of altered mtDNA in strabismus and its possible significance with regard to the etiology of strabismus.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104042"},"PeriodicalIF":1.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142631814","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Elevated intraocular pressure in a child with Stickler syndrome after scleral buckle surgery for retinal detachment. 一名患有 Stickler 综合征的儿童在接受巩膜扣带手术治疗视网膜脱离后眼压升高。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-12-01 Epub Date: 2024-11-14 DOI: 10.1016/j.jaapos.2024.104043
Abdelrahman M Anter, Seyyedehfatemeh Ghalibafan, Louis Z Cai, Connie M Wu, Elena Bitrian, Nicolas A Yannuzzi
{"title":"Elevated intraocular pressure in a child with Stickler syndrome after scleral buckle surgery for retinal detachment.","authors":"Abdelrahman M Anter, Seyyedehfatemeh Ghalibafan, Louis Z Cai, Connie M Wu, Elena Bitrian, Nicolas A Yannuzzi","doi":"10.1016/j.jaapos.2024.104043","DOIUrl":"10.1016/j.jaapos.2024.104043","url":null,"abstract":"<p><p>Stickler syndrome, a rare connective tissue disorder, presents with a broad spectrum of ocular manifestations, including myopia, vitreoretinal degeneration, glaucoma, and retinal detachment. While extensive data exists on the treatment outcomes of retinal detachment repair in Stickler syndrome, the potential risks associated with acute postoperative intraocular pressure elevation remain underexplored. We report the case of a 10-year-old boy with Stickler syndrome who underwent scleral buckling surgery and subsequently experienced ocular hypertension.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104043"},"PeriodicalIF":1.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142640181","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Term infant brain MRI after ROP treatment by anti-VEGF injection versus laser therapy. 抗血管内皮生长因子注射与激光疗法治疗视网膜病变后的足月婴儿脑磁共振成像。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-12-01 Epub Date: 2024-11-14 DOI: 10.1016/j.jaapos.2024.104038
Monica Manrique, Michael Pham, Sudeepta Basu, Jonathan Murnick, Md Sohel Rana, Taeun Chang, Christabel Chan, Emile Vieta-Ferrer, Catherine Sano, Catherine Limperopoulos, Marijean Miller
{"title":"Term infant brain MRI after ROP treatment by anti-VEGF injection versus laser therapy.","authors":"Monica Manrique, Michael Pham, Sudeepta Basu, Jonathan Murnick, Md Sohel Rana, Taeun Chang, Christabel Chan, Emile Vieta-Ferrer, Catherine Sano, Catherine Limperopoulos, Marijean Miller","doi":"10.1016/j.jaapos.2024.104038","DOIUrl":"10.1016/j.jaapos.2024.104038","url":null,"abstract":"<p><strong>Background: </strong>Intravitreal injection of anti-vascular endothelial growth factor (anti-VEGF) agents is used to treat posterior type 1 retinopathy of prematurity (ROP). Recent reports indicate that anti-VEGF therapy may be associated with white matter brain injury, according to animal studies, and neurodevelopmental impairments in children born preterm. We investigated whether type 1 ROP treated with bevacizumab is associated with structural brain injury on infant term magnetic resonance images (MRIs) in very low birth weight infants compared with those treated with laser ablation.</p><p><strong>Methods: </strong>We retrospectively reviewed the medical records of very low birth weight infants from 2006 to 2021 with type 1 ROP who had been treated with laser or anti-VEGF therapy. Intravitreal bevacizumab injection was used for type 1 ROP in zone 1 or very posterior zone 2 or when laser treatment was not feasible. A pediatric neuroradiologist reviewed brain MRIs at term equivalent age (36-46 weeks' postmenstrual age) and classified infants for severity (no/mild vs moderate/severe) of overall brain and white matter injury using the validated Kidokoro scoring system.</p><p><strong>Results: </strong>Fifty-two infants met inclusion criteria: 35 (67%) treated with laser and 17 (33%) with bevacizumab. Moderate-to-severe brain injury scores were not statistically different between bevacizumab and laser treatment groups in either continuous or binary adjusted analyses, for either the overall score or the white matter subscore.</p><p><strong>Conclusions: </strong>Severity of structural injury on term brain MRI (total and white matter) did not differ between infants with type 1 ROP treated with anti-VEGF agent (bevacizumab) and those treated with laser ablation.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104038"},"PeriodicalIF":1.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142644731","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Access to vision care for children from immigrant and nonimmigrant households: evidence from the National Survey of Children's Health 2018-2019. 移民和非移民家庭儿童获得视力保健的机会:来自 2018-2019 年全国儿童健康调查的证据。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-12-01 Epub Date: 2024-11-14 DOI: 10.1016/j.jaapos.2024.104044
Afua O Asare, Brian C Stagg, Carole Stipelman, Heather T Keenan, Melissa Watt, Guilherme Del Fiol, Marielle P Young, Justin D Smith
{"title":"Access to vision care for children from immigrant and nonimmigrant households: evidence from the National Survey of Children's Health 2018-2019.","authors":"Afua O Asare, Brian C Stagg, Carole Stipelman, Heather T Keenan, Melissa Watt, Guilherme Del Fiol, Marielle P Young, Justin D Smith","doi":"10.1016/j.jaapos.2024.104044","DOIUrl":"10.1016/j.jaapos.2024.104044","url":null,"abstract":"<p><strong>Purpose: </strong>To investigate whether immigrant generation is associated with caregiver-reported receipt of vision testing.</p><p><strong>Methods: </strong>Nationally representative data from the 2018-2019 National Survey of Children's Health was used. The primary exposure was immigrant generation, with first generation defined as child and all reported parents born outside the United States; second generation, as child born in the United States but at least one parent born outside the United States; and third generation, as all parents in the household born in the United States. The main outcome was caregiver-reported vision testing during the previous 12 months. Odds ratios adjusted for sociodemographic characteristics and 95% confidence intervals were computed based on immigrant generation.</p><p><strong>Results: </strong>The sample included 49,442 US children 3-17 years of age. The proportion of children who had vision testing in any setting was lower for first- (60.3%) than third-generation children (74.6%; aOR = 0.54; 95% CI, 0.41-0.71). This association remained after excluding children without health coverage. For Hispanic children, both first- (aOR = 0.58; 95% CI, 0.36-0.94) and second-generation children (aOR = 0.73; 95% CI, 0.55-0.96) had lower odds of a vision test in any setting compared with third-generation Hispanic children.</p><p><strong>Conclusions: </strong>First-generation children had lower odds of vision testing than third-generation children, even when adjusting for sociodemographic characteristics, especially in Hispanic households.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104044"},"PeriodicalIF":1.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11645187/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142644672","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A rare case of infantile acute polymicrobial dacryocystitis due to Serratia marcescens, Haemophilus aphrophilus, and Prevotellaintermedia. 一例罕见的婴幼儿急性多菌性泪囊炎病例,病原体包括大肠沙雷氏菌、阿弗氏嗜血杆菌和中间普雷沃特氏菌。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-12-01 Epub Date: 2024-10-16 DOI: 10.1016/j.jaapos.2024.104019
Marina Shenouda, Agni Kakouri, Timothy J McCulley, Ying Chen
{"title":"A rare case of infantile acute polymicrobial dacryocystitis due to Serratia marcescens, Haemophilus aphrophilus, and Prevotellaintermedia.","authors":"Marina Shenouda, Agni Kakouri, Timothy J McCulley, Ying Chen","doi":"10.1016/j.jaapos.2024.104019","DOIUrl":"10.1016/j.jaapos.2024.104019","url":null,"abstract":"<p><p>Infantile acute dacryocystitis is an acute inflammation of the lacrimal sac in infants. The most common pathogens are Gram-positive cocci and Gram-negative rods. We report a case of infantile polymicrobial acute dacryocystitis. A 6-week-old girl presented emergently with eye edema, discharge, and fever. Symptoms resolved with nasolacrimal probing and systemic antibiotics. Intraoperative cultures were positive for Serratia marcescens, Haemophilus aphrophilus, and Prevotella intermedia. This case highlights the importance of considering uncommon pathogens in the etiology of infantile dacryocystitis.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104019"},"PeriodicalIF":1.2,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142479610","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acute and chronic optical coherence tomography findings in partial optic nerve head avulsion. 视神经头部分撕脱的急性和慢性光学相干断层扫描结果。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-11-26 DOI: 10.1016/j.jaapos.2024.104060
Hari R Anandarajah, Steven Seto, Roxana Y Godiwalla, Smith Ann M Chisholm, Judy E Kim, Ryan D Walsh
{"title":"Acute and chronic optical coherence tomography findings in partial optic nerve head avulsion.","authors":"Hari R Anandarajah, Steven Seto, Roxana Y Godiwalla, Smith Ann M Chisholm, Judy E Kim, Ryan D Walsh","doi":"10.1016/j.jaapos.2024.104060","DOIUrl":"10.1016/j.jaapos.2024.104060","url":null,"abstract":"<p><p>We present a case of partial optic nerve head (ONH) avulsion in a 15-year-old boy evaluated with optical coherence tomography (OCT) from 2 weeks to 15 months after acute injury. Distinct findings on OCT in the acute setting correlated with the diagnosis and with additional testing, including fundus photography, Humphrey visual fields, and clinical examination. OCT findings became less pronounced in the chronic setting. Our case highlights that OCT may be valuable in the acute setting for evaluating ONH avulsion in certain patients; however, OCT findings are less distinct in the chronic setting.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104060"},"PeriodicalIF":1.2,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142741011","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ocular manifestations of SREBF1-associated hereditary mucoepithelial dysplasia. SREBF1相关遗传性粘液上皮发育不良的眼部表现。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-11-26 DOI: 10.1016/j.jaapos.2024.104059
Whitney Stuard Sambhariya, Jefferson Doyle, Courtney L Kraus
{"title":"Ocular manifestations of SREBF1-associated hereditary mucoepithelial dysplasia.","authors":"Whitney Stuard Sambhariya, Jefferson Doyle, Courtney L Kraus","doi":"10.1016/j.jaapos.2024.104059","DOIUrl":"10.1016/j.jaapos.2024.104059","url":null,"abstract":"<p><p>Hereditary mucoepithelial dysplasia (HMD) is a rare autosomal dominant dysplastic dyskeratotic epithelial syndrome caused by pathogenic variants in the SREBF1 gene. This syndrome is associated with a variety of ocular conditions, including cataracts, nystagmus, keratitis, meibomian gland dysfunction (MGD), and decreased visual acuity. We report the case of a boy followed from 1 to 7 years of age who had a confirmed HMD-associated variant in the SREBF1 gene. The patient has severe MGD, with resulting keratitis and photosensitivity, and bilateral glaucoma, which has not previously been reported in association with HMD. The gene affected in HMD negatively affects gap junctions and lipid biosynthesis, which are important in the stability of the trabecular meshwork.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104059"},"PeriodicalIF":1.2,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142741122","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Abducens nerve palsy: a rare copresenting sign of incomplete Kawasaki Disease. 外展神经麻痹:不完全性川崎病罕见的共同表现。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-11-26 DOI: 10.1016/j.jaapos.2024.104061
Jennifer M Lai, Dallin C Milner, Ryan Frisbie, Michael A Puente
{"title":"Abducens nerve palsy: a rare copresenting sign of incomplete Kawasaki Disease.","authors":"Jennifer M Lai, Dallin C Milner, Ryan Frisbie, Michael A Puente","doi":"10.1016/j.jaapos.2024.104061","DOIUrl":"10.1016/j.jaapos.2024.104061","url":null,"abstract":"<p><p>A 21-month-old girl presented with acute-onset esotropia with unexplained fever, conjunctivitis, and rash. Sensorimotor examination revealed the presence of a left abducens nerve palsy. After cardiogenic shock, she was found to have multiple large coronary artery aneurysms and was diagnosed with incomplete Kawasaki disease. The patient eventually had near-resolution of her abducens nerve palsy with treatment for her underlying Kawasaki disease through aspirin, infliximab, and intravenous immunoglobulin therapy. Abducens nerve palsy is a rare manifestation of Kawasaki disease that may reflect a late diagnosis and an increased risk of coronary artery involvement.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104061"},"PeriodicalIF":1.2,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142752207","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Orbital hematoma due to vitamin K deficiency in an infant. 婴儿因缺乏维生素 K 而导致眼眶血肿。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-11-19 DOI: 10.1016/j.jaapos.2024.104055
Neelam Pushker, Punya Muralidhar, Rachna Meel, Bhupendra Yadav
{"title":"Orbital hematoma due to vitamin K deficiency in an infant.","authors":"Neelam Pushker, Punya Muralidhar, Rachna Meel, Bhupendra Yadav","doi":"10.1016/j.jaapos.2024.104055","DOIUrl":"10.1016/j.jaapos.2024.104055","url":null,"abstract":"<p><p>We report a rare case of late-onset vitamin K deficiency bleeding in a 3-month-old boy who presented with orbital compartment syndrome due to massive bleed in the right orbit. The coagulation profile was highly abnormal. The patient was treated with vitamin K injections, following which the coagulation profile normalized. The orbital hematoma required drainage because of severe proptosis with orbital compartment syndrome. The patient subsequently developed a corneal opacity, but there was no recurrence of bleeding.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104055"},"PeriodicalIF":1.2,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142683097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Using machine learning to identify pediatric ophthalmologists. 利用机器学习识别儿科眼科医生。
IF 1.2 4区 医学
Journal of Aapos Pub Date : 2024-11-19 DOI: 10.1016/j.jaapos.2024.104052
Isdin Oke, Tobias Elze, Joan W Miller, Alice C Lorch, Mei-Sing Ong, Ann Chen Wu, David G Hunter
{"title":"Using machine learning to identify pediatric ophthalmologists.","authors":"Isdin Oke, Tobias Elze, Joan W Miller, Alice C Lorch, Mei-Sing Ong, Ann Chen Wu, David G Hunter","doi":"10.1016/j.jaapos.2024.104052","DOIUrl":"10.1016/j.jaapos.2024.104052","url":null,"abstract":"<p><p>This cross-sectional study used data from the American Academy of Ophthalmology IRIS Registry (Intelligent Research in Sight) and machine learning algorithms to identify pediatric ophthalmologists based on physician coding patterns. A random forest model achieved an area under the receiver operating characteristic curve of 0.98, sensitivity of 0.98, and specificity of 0.88 when classifying pediatric eye specialists in the test validation cohort. Algorithm-based approaches to identify pediatric ophthalmologists using procedure codes may offer new avenues to determine the scope, scale, and trajectory of pediatric eye care delivery.</p>","PeriodicalId":50261,"journal":{"name":"Journal of Aapos","volume":" ","pages":"104052"},"PeriodicalIF":1.2,"publicationDate":"2024-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142683202","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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
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