Erita相关文献与解析，生知库 | 链接生命科学的每一步

Understanding Health Care Students' Perceptions, Beliefs, and Attitudes Toward AI-Powered Language Models: Cross-Sectional Study

了解医护专业学生对人工智能语言模型的认知、信念和态度：一项横断面研究

Cherrez-Ojeda, Ivan; Gallardo-Bastidas, Juan C; Robles-Velasco, Karla; Osorio, María F; Velez Leon, Eleonor Maria; Leon Velastegui, Manuel; Pauletto, Patrícia; Aguilar-Díaz, F C; Squassi, Aldo; González Eras, Susana Patricia; Cordero Carrasco, Erita; Chavez Gonzalez, Karol Leonor; Calderon, Juan C; Bousquet, Jean; Bedbrook, Anna; Faytong-Haro, Marco

神经科学

发表日期：2024

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Aicardi-Goutières Syndrome with Congenital Glaucoma Caused by Novel TREX1 Mutation

由新型TREX1突变引起的伴有先天性青光眼的艾卡迪-古蒂埃综合征

期刊:Journal of Personalized Medicine

影响因子:3

doi:10.3390/jpm13111609

Świerczyńska, Marta; Tronina, Agnieszka; Filipek, Erita

Analysis of Peripapillary Retinal Nerve Fiber Layer Thickness in Acute Anterior Uveitis among Children with HLA-B27-Positive Juvenile Idiopathic Arthritis

对 HLA-B27 阳性幼年特发性关节炎患儿急性前葡萄膜炎中视乳头周围视网膜神经纤维层厚度的分析

期刊:Journal of Clinical Medicine

影响因子:2.9

doi:10.3390/jcm12144842

Świerczyńska, Marta; Tronina, Agnieszka; Filipek, Erita

关节炎

发表日期：2023

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First Case Report of Developmental Bilateral Cataract with a Novel Mutation in the ZEB2 Gene Observed in Mowat-Wilson Syndrome

莫瓦特-威尔逊综合征中发现的ZEB2基因新突变导致发育性双侧白内障的首例病例报告

期刊:Medicina-Lithuania

影响因子:2.4

doi:10.3390/medicina59010101

Tronina, Agnieszka; Świerczyńska, Marta; Filipek, Erita

Anterior Uveitis and Coats Disease in a 16-Year-Old Girl with Noonan Syndrome-A Case Report

16岁努南综合征女孩合并前葡萄膜炎和科茨病——病例报告

期刊:Children-Basel

影响因子:2.1

doi:10.3390/children10101643

Świerczyńska, Marta; Tronina, Agnieszka; Lorenc, Anna; Filipek, Erita

发表日期：2023

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Evaluation of Macular Ganglion Cell-Inner Plexiform Layer in Children with Deprivational Amblyopia Who Underwent Unilateral Cataract Surgery

对接受单侧白内障手术的剥夺性弱视患儿黄斑神经节细胞-内丛状层进行评估

期刊:Medicina-Lithuania

影响因子:2.4

doi:10.3390/medicina59010013

Świerczyńska, Marta; Tronina, Agnieszka; Filipek-Janiszewski, Bartosz; Filipek, Erita

Ocular features in Aicardi syndrome: A case report

Aicardi综合征的眼部特征：病例报告

期刊:Medicine

影响因子:1.4

doi:10.1097/MD.0000000000031950

Sirek, Sebastian; Filipek, Erita; Wójcik-Niklewska, Bogumiła; Pojda-Wilczek, Dorota; Mrukwa-Kominek, Ewa

发表日期：2022

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A Clinical Study of the Impact of Soft Contact Lenses on the Progression of Myopia in Young Patients

软性隐形眼镜对青少年近视进展影响的临床研究

期刊:

影响因子:

doi:10.2147/OPTH.S338199

Malinowski, Andrzej; Mrugacz, Małgorzata; Stopa, Marcin; Filipek, Erita; Moniuszko-Malinowska, Anna; Czupryna, Piotr

发表日期：2022

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Corneal Cross-Linking for Pediatric Keratoconus

儿童圆锥角膜的角膜交联术

Mowat-Wilson syndrome: Case report

莫瓦特-威尔逊综合征：病例报告

Understanding Health Care Students' Perceptions, Beliefs, and Attitudes Toward AI-Powered Language Models: Cross-Sectional Study

了解医护专业学生对人工智能语言模型的认知、信念和态度：一项横断面研究

Aicardi-Goutières Syndrome with Congenital Glaucoma Caused by Novel TREX1 Mutation

由新型TREX1突变引起的伴有先天性青光眼的艾卡迪-古蒂埃综合征

Analysis of Peripapillary Retinal Nerve Fiber Layer Thickness in Acute Anterior Uveitis among Children with HLA-B27-Positive Juvenile Idiopathic Arthritis

对 HLA-B27 阳性幼年特发性关节炎患儿急性前葡萄膜炎中视乳头周围视网膜神经纤维层厚度的分析

First Case Report of Developmental Bilateral Cataract with a Novel Mutation in the ZEB2 Gene Observed in Mowat-Wilson Syndrome

莫瓦特-威尔逊综合征中发现的ZEB2基因新突变导致发育性双侧白内障的首例病例报告

Anterior Uveitis and Coats Disease in a 16-Year-Old Girl with Noonan Syndrome-A Case Report

16岁努南综合征女孩合并前葡萄膜炎和科茨病——病例报告

Evaluation of Macular Ganglion Cell-Inner Plexiform Layer in Children with Deprivational Amblyopia Who Underwent Unilateral Cataract Surgery

对接受单侧白内障手术的剥夺性弱视患儿黄斑神经节细胞-内丛状层进行评估

Ocular features in Aicardi syndrome: A case report

Aicardi综合征的眼部特征：病例报告

A Clinical Study of the Impact of Soft Contact Lenses on the Progression of Myopia in Young Patients

软性隐形眼镜对青少年近视进展影响的临床研究