GMS ophthalmology cases最新文献

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Unilateral macular neovascularization formation during the follow-up of a 15-year-old boy with Bietti crystalline dystrophy and the successful treatment outcome with a single intravitreal ranibizumab injection. 一名15岁男孩Bietti结晶性营养不良的随访期间单侧黄斑新生血管的形成和单次玻璃体内注射兰珠单抗的成功治疗结果。
GMS ophthalmology cases Pub Date : 2023-01-01 DOI: 10.3205/oc000214
Mustafa Kayabaşi, Ferdane Ataş, Ali Osman Saatci
{"title":"Unilateral macular neovascularization formation during the follow-up of a 15-year-old boy with Bietti crystalline dystrophy and the successful treatment outcome with a single intravitreal ranibizumab injection.","authors":"Mustafa Kayabaşi,&nbsp;Ferdane Ataş,&nbsp;Ali Osman Saatci","doi":"10.3205/oc000214","DOIUrl":"https://doi.org/10.3205/oc000214","url":null,"abstract":"<p><strong>Objective: </strong>To report the successful outcome with a single intravitreal ranibizumab injection in a 15-year-old boy with Bietti crystalline dystrophy (BCD) who developed a unilateral macular neovascularization (MNV).</p><p><strong>Methods: </strong>A retrospective case report.</p><p><strong>Results: </strong>A 15-year-old Caucasian boy with Bietti crystalline dystrophy was diagnosed to have a unilateral MNV a year after the initial examination with the help of multimodal imaging and he was treated with a single intravitreal ranibizumab injection. Five months later, visual acuity improved and anatomically a dry-looking macula was noted.</p><p><strong>Conclusion: </strong>MNV is among the rare macular complications of BCD. The present case is the third reported pediatric case with MNV in association with BCD and the first pediatric BCD patient who received a vascular endothelial growth factor inhibitor (anti-VEGF) agent.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"13 ","pages":"Doc06"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073982/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9278949","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
Unilateral K-F ring in Wilson's disease. Wilson病的单侧K-F环。
GMS ophthalmology cases Pub Date : 2023-01-01 DOI: 10.3205/oc000216
Shruti P Hegde, Sakthivel Senthil Kumar
{"title":"Unilateral K-F ring in Wilson's disease.","authors":"Shruti P Hegde,&nbsp;Sakthivel Senthil Kumar","doi":"10.3205/oc000216","DOIUrl":"https://doi.org/10.3205/oc000216","url":null,"abstract":"<p><p>Wilson's disease, also called hepatolenticular degeneration, has varied clinical manifestations and poses diagnostic challenges. Kayser-Fleischer ring, when present, is considered pathognomic of Wilson's disease. Although its presence is most commonly seen with the neuro-psychiatric form of the disease, it can also be present in hepatic form and asymptomatic patients. We report a case of unilateral Kayser-Fleischer ring in the normal, functional eye of a patient which subsequently led to the diagnosis of Wilson's disease in the patient. This case also highlights the examination of the normal appearing eye in all the patients presenting with complaints in only one eye.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"13 ","pages":"Doc08"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073984/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9273587","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
Microscope integrated OCT (Mi-OCT) guided retrieval of intrastromal corneal foreign body. 显微集成OCT (Mi-OCT)引导下角膜基质内异物取出术。
GMS ophthalmology cases Pub Date : 2023-01-01 DOI: 10.3205/oc000217
Ashish Markan, Kiran Chandra, Ramandeep Singh, Mohit Dogra
{"title":"Microscope integrated OCT (Mi-OCT) guided retrieval of intrastromal corneal foreign body.","authors":"Ashish Markan,&nbsp;Kiran Chandra,&nbsp;Ramandeep Singh,&nbsp;Mohit Dogra","doi":"10.3205/oc000217","DOIUrl":"https://doi.org/10.3205/oc000217","url":null,"abstract":"<p><strong>Introduction: </strong>To describe the role of microscope integrated optical tomography (Mi-OCT) in removal of intrastromal corneal foreign body.</p><p><strong>Methodology: </strong>A young male presented with trauma to the right eye with sugarcane stick. Ocular examination revealed two sugarcane particles, approximately 3.5 mm in greatest dimension, embedded in the corneal stroma. For removal of foreign body, Mi-OCT was switched on and the area of interest was focused. Sugarcane particles appeared as hyperreflective structures embedded in the corneal stroma with everted edges of the overlying corneal epithelium and anterior stroma.</p><p><strong>Results: </strong>Both the sugarcane particles were removed successfully under real time images provided by Mi-OCT without causing any inadvertent damage to the corneal stroma.</p><p><strong>Conclusion: </strong>Mi-OCT can be used as an adjunct in emergency surgical procedures like removal of intrastromal corneal foreign bodies with accurate precision.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"13 ","pages":"Doc09"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073981/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9273590","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
Self-inflicted bilateral ocular injury with scissors in a psychiatric patient. 精神病人用剪刀自残双眼。
GMS ophthalmology cases Pub Date : 2023-01-01 DOI: 10.3205/oc000219
Jigyasa Sahu, Ritu Arora, Shweta Vishwanath
{"title":"Self-inflicted bilateral ocular injury with scissors in a psychiatric patient.","authors":"Jigyasa Sahu,&nbsp;Ritu Arora,&nbsp;Shweta Vishwanath","doi":"10.3205/oc000219","DOIUrl":"https://doi.org/10.3205/oc000219","url":null,"abstract":"<p><p>A young male was brought to the ophthalmic emergency by his family with severe bleeding from both eyes after self-inflicted injury with scissors in a fit of mania. He had a history of schizophrenia and has been on irregular treatment for the past 10 years. Both eyes were severely damaged with avulsion of all extraocular muscles in one eye and a large corneoscleral laceration in the other. We report this unique case of oedipism or self-enucleation where a sharp instrument was used. Self-inflicted injury to the eyes is a rather uncommon phenomenon described in psychiatric patients. It can range from minor abrasions to severe ocular mutilation and loss of sight. The strict observation of these patients while admitted to the hospital and a multidisciplinary approach to ensure their future safety are imperative.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"13 ","pages":"Doc11"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227493/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9571284","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
Pseudomelanoma: occult intraocular foreign body mimicking choroidal melanoma. 假性黑色素瘤:隐匿的眼内异物,类似脉络膜黑色素瘤。
GMS ophthalmology cases Pub Date : 2023-01-01 DOI: 10.3205/oc000211
Aslıhan Yılmaz Çebi, Bilge Batu Oto, Oğuzhan Kılıçarslan, Ahmet Murat Sarıcı
{"title":"Pseudomelanoma: occult intraocular foreign body mimicking choroidal melanoma.","authors":"Aslıhan Yılmaz Çebi,&nbsp;Bilge Batu Oto,&nbsp;Oğuzhan Kılıçarslan,&nbsp;Ahmet Murat Sarıcı","doi":"10.3205/oc000211","DOIUrl":"https://doi.org/10.3205/oc000211","url":null,"abstract":"<p><strong>Purpose: </strong>To report an occult intraocular foreign body mimicking choroidal melanoma.</p><p><strong>Methods: </strong>Medical records and imagings of the patient were retrospectively reviewed.</p><p><strong>Case description: </strong>A 76-year-old male was referred to our ocular oncology clinic with a suspicious hyperpigmented retinal lesion in the left eye. Biomicroscopy showed aphakia and peripheral iridectomy in the left eye. Fundoscopy revealed a pigmented, slightly elevated lesion on the macula of the left eye surrounded by diffuse atrophy. B-scan ultrasonography showed a preretinal hyperechoic lesion with posterior shadowing. There was no choroidal mass in B-scan or optical coherence tomography (OCT) imaging. On further questioning, it was disclosed that the patient had been hit by an iron fragment in the left eye forty years ago.</p><p><strong>Conclusion: </strong>Choroidal melanoma is a vision- and life-threatening intraocular malignant tumour. Various neoplastic, degenerative, and inflammatory conditions can simulate choroidal melanoma. A previous history of penetrating ocular trauma should lead the surgeon to re-evaluate a diagnosis of melanoma.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"13 ","pages":"Doc03"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979075/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10838267","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
Staged limbal stem cell transplantation and keratoplasty surgeries as a treatment for gelatinous drop-like corneal dystrophy. 分期角膜缘干细胞移植和角膜移植手术治疗胶质滴状角膜营养不良。
GMS ophthalmology cases Pub Date : 2023-01-01 DOI: 10.3205/oc000210
Tayaba N Azher, Amanda C Maltry, Joshua H Hou
{"title":"Staged limbal stem cell transplantation and keratoplasty surgeries as a treatment for gelatinous drop-like corneal dystrophy.","authors":"Tayaba N Azher,&nbsp;Amanda C Maltry,&nbsp;Joshua H Hou","doi":"10.3205/oc000210","DOIUrl":"https://doi.org/10.3205/oc000210","url":null,"abstract":"<p><p>Gelatinous drop-like corneal dystrophy (GDLD) is a rare autosomal recessive corneal dystrophy that has been associated with mutations in the TACSTD2 (M1S1) gene, which is normally expressed in corneal epithelial cells. GDLD is characterized by progressive deposition of amyloid in the corneal stroma with rapid recurrence in grafts after penetrating keratoplasty. We report of case of a patient with GDLD treated bilaterally with staged limbal stem cell transplantation and penetrating keratoplasty that resulted in long-term control of his disease. This case demonstrates that staged allogenic limbal stem cell transplantation, before or after penetrating keratoplasty, can be used to restore vision long-term in GDLD patients.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"13 ","pages":"Doc02"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979074/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10838262","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
Enhancing the knowledge in fundus autofluorescence of optic nerve head drusen assessed with broad line fundus imaging technology. 阔线眼底成像技术提高对视神经头眼底自身荧光的认识。
GMS ophthalmology cases Pub Date : 2023-01-01 DOI: 10.3205/oc000222
Gabriel Castilho Sandoval Barbosa, Leandro C Zacharias, Eduardo A Novais, Ricardo L L Guerra
{"title":"Enhancing the knowledge in fundus autofluorescence of optic nerve head drusen assessed with broad line fundus imaging technology.","authors":"Gabriel Castilho Sandoval Barbosa,&nbsp;Leandro C Zacharias,&nbsp;Eduardo A Novais,&nbsp;Ricardo L L Guerra","doi":"10.3205/oc000222","DOIUrl":"https://doi.org/10.3205/oc000222","url":null,"abstract":"The concept of retinal autofluorescence (AF) came to light in the 1970s when an autofluorescent signal of optic nerve head drusen (ONHD) was noted prior to the injection of fluorescein dye [1]. Nowadays, several devices offer distinct methods for acquiring short-wave fundus autofluorescence (SW-FAF) images, all of them being clinically useful in assessing the presence of lipofuscin, a naturally occurring ocular fluorophor which reflects the general health of the photoreceptor and retinal pigment epithelium (RPE). Each device provides a different image acquisition method; thus, discrepancies exist in the images obtained. For example, fundus cameras feature a high-energy white flash that streams through a wideband excitation filter and a series of mirrors and apertures to obtain images. On the other hand, confocal scanning laser ophthalmoscope (cSLO) emits a single wavelength, which will only excite fluorophores that absorb light with a peak excitation near that specific wavelength [2]. Broad line fundus image (BLFI) technique is a hybrid of both cSLO and traditional fundus photography. By utilizing line scanning illuminationwith light-emitting diodes (LEDs) and an aperture confocal to the illumination, this system illuminates and detects retinal images in two wavelength ranges: fundus autofluorescence (FAF)-Blue (435–500 nm) and FAF-Green (500–585 nm) [3]. Both are categorized as short-wavelength, but it is well known that green light can reach deeper layers of the retina, being absorbed less by the luteal pigments of themacula, and allowing a better definition of lesions in the underlying RPE. ONHD are a form of calcific degeneration in some of the axons of the optic nerve that may give a swollen-looking appearance, and are usually formed early in life. ONHD are diagnosed with fundoscopic examination, but some casesmay require B-scan ultrasonography, AF, and optical coherence tomography (OCT) to confirm the lesion [4]. The features of ONHD in FAF imaging are well described in many previous publications [4], [5]. Yan et al. [4] recently described the peculiarities of ONHD in FAF-Blue and -Green by using a cSLO system from two different devices. Despite a considerable amount of meaningful information, we were unable to find a description of FAF imaging in ONHD using BLFI technology in the literature. We have recently observed a noticeable disparity in the","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":"13 ","pages":"Doc14"},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10413383/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10000996","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
Successful management of recalcitrant fungal keratitis with topical caspofungin. 外用卡泊霉素成功治疗顽固性真菌性角膜炎。
GMS ophthalmology cases Pub Date : 2022-07-18 eCollection Date: 2022-01-01 DOI: 10.3205/oc000206
Siddhi Goel, Arpit Sharma, Rajesh Sinha
{"title":"Successful management of recalcitrant fungal keratitis with topical caspofungin.","authors":"Siddhi Goel,&nbsp;Arpit Sharma,&nbsp;Rajesh Sinha","doi":"10.3205/oc000206","DOIUrl":"https://doi.org/10.3205/oc000206","url":null,"abstract":"<p><strong>Objective: </strong>To report a case of recalcitrant fungal keratitis successfully managed with topical caspofungin acetate in North India.</p><p><strong>Methods: </strong>Case report and literature review.</p><p><strong>Results: </strong>An 18-year-old male patient presented with complaints of redness, watering, pain and diminution of vision in the right eye and was referred to our centre as a case of corneal ulcer. The patient was examined and found to have a near total epithelial defect, with corneal infiltrates approximately 8x8 mm. A provisional diagnosis of polymicrobial keratitis was made based on corneal scraping suggestive of <i>S</i> <i>tap</i> <i>h</i> <i>ylococcus aureus</i> and confocal scan revealing fungal hyphae. The patient failed to respond to topical voriconazole 1%, natamycin 5% and moxifloxacin hydrochloride 0.5% with oral voriconazole. In view of the poor response to these drugs, the patient was subsequently administered topical caspofungin 0.5% in place of natamycin and continued on topical and oral voriconazole, in addition to topical moxifloxacin and cycloplegics, which finally led to healing with minimal scarring. The patient attained a best corrected visual acuity (BCVA) of 6/12.</p><p><strong>Conclusion: </strong>Topical caspofungin may be used as a useful and effective alternative in cases of recalcitrant fungal keratitis. It may result in healing with minimal scarring.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":" ","pages":"Doc19"},"PeriodicalIF":0.0,"publicationDate":"2022-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577386/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40438174","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
Combined central retinal artery and vein occlusion following trabeculectomy. 小梁切除术后视网膜中央动静脉联合闭塞。
GMS ophthalmology cases Pub Date : 2022-06-28 eCollection Date: 2022-01-01 DOI: 10.3205/oc000205
Albert John Bromeo, Sweet Jorlene Lerit, Patricia Grulla-Quilendrino, George Michael Sosuan, Edgar Leuenberger
{"title":"Combined central retinal artery and vein occlusion following trabeculectomy.","authors":"Albert John Bromeo,&nbsp;Sweet Jorlene Lerit,&nbsp;Patricia Grulla-Quilendrino,&nbsp;George Michael Sosuan,&nbsp;Edgar Leuenberger","doi":"10.3205/oc000205","DOIUrl":"https://doi.org/10.3205/oc000205","url":null,"abstract":"<p><p>Retinal vascular events may occur as rare complications of glaucoma procedures due to various factors, including exacerbation of ischemia in patients with pre-existing vascular comorbidities, toxic effect of mitomycin-C, and decompression retinopathy. We present the case of a 47-year-old hypertensive male who underwent trabeculectomy for advanced glaucoma in his right eye. At 3 weeks postoperatively, he presented with a drop in visual acuity to light perception with a spike in intraocular pressure. On examination, there was increased bleb vascularity as well as rubeosis. Fundoscopy revealed findings consistent with both central retinal artery occlusion and central retinal vein occlusion. Combined central retinal artery and vein occlusion is a rare retinal vascular condition. Neovascular glaucoma can occur as a sequelae of the ischemic process in the retina. Despite treatment, there is a poor visual prognosis, with the affected eye usually becoming blind from optic atrophy and neovascularization.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":" ","pages":"Doc18"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285110/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40574969","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
Unusual extraconal orbital location of a cavernous hemangioma. 海绵状血管瘤的异常眶外位置。
GMS ophthalmology cases Pub Date : 2022-06-10 eCollection Date: 2022-01-01 DOI: 10.3205/oc000204
Gabriela Pacheco Callirgos, Francisco Javier Valentín Bravo, Pablo Panadero Meseguer, Víctor Manuel Asensio Sánchez
{"title":"Unusual extraconal orbital location of a cavernous hemangioma.","authors":"Gabriela Pacheco Callirgos,&nbsp;Francisco Javier Valentín Bravo,&nbsp;Pablo Panadero Meseguer,&nbsp;Víctor Manuel Asensio Sánchez","doi":"10.3205/oc000204","DOIUrl":"https://doi.org/10.3205/oc000204","url":null,"abstract":"<p><p>Cavernous hemangioma is the most common benign orbital and vascular tumor in adults. It is mostly located intraconally. Nevertheless, when the location is extraconal, the displacement of the globe is opposite the tumor's position. We describe an unusual presentation of this tumor in a 75-year-old female. The only symptom was the presence of epiphora. In the clinical examination, a mass was palpated on the lower orbital rim of the right eye. The magnetic resonance imaging (MRI) showed a well-circumscribed ovoid mass with a strong T2 hyperintensity and progressive contrast filling in T1. Excisional biopsy was performed, which confirmed the diagnosis of cavernous hemangioma. At five months of follow-up, there was no evidence of new symptoms.</p>","PeriodicalId":73178,"journal":{"name":"GMS ophthalmology cases","volume":" ","pages":"Doc17"},"PeriodicalIF":0.0,"publicationDate":"2022-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9285109/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40572438","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
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