081. Spontaneous Regression of Secondary Vitreoretinal Lymphoma after Diagnostic Vitrectomy: Case Report

yuping.zhou2023-07-14T15:13:59+08:00

081. Spontaneous Regression of Secondary Vitreoretinal Lymphoma after Diagnostic Vitrectomy: Case Reportyuping.zhou2023-07-14T15:13:59+08:00

075. Papillary Vitreous Detachment as a Possible Accomplice in Non-Arteritic Anterior Ischaemic Optic Neuropathy

yuping.zhou2023-07-14T14:40:09+08:00

075. Papillary Vitreous Detachment as a Possible Accomplice in Non-Arteritic Anterior Ischaemic Optic Neuropathyyuping.zhou2023-07-14T14:40:09+08:00

074. Large Colloid Drusen

yiqi.zhang2023-07-13T13:35:50+08:00

074. Large Colloid Drusenyiqi.zhang2023-07-13T13:35:50+08:00

065. The Genetic Spectrum and Clinical Features of X-Linked Juvenile Retinoschisis in Central China

yiqi.zhang2023-04-18T17:27:11+08:00

065. The Genetic Spectrum and Clinical Features of X-Linked Juvenile Retinoschisis in Central Chinayiqi.zhang2023-04-18T17:27:11+08:00

064. The Clinical Characteristics of Streaky Multifocal Choroiditis (SMFC): A Subtype of Multifocal Choroiditis

yiqi.zhang2023-02-13T11:55:15+08:00

064. The Clinical Characteristics of Streaky Multifocal Choroiditis (SMFC): A Subtype of Multifocal Choroiditisyiqi.zhang2023-02-13T11:55:15+08:00

061. Characteristics and Classification of Choroidal Caverns in Patients with Various Retinal and Chorioretinal Diseases

yiqi.zhang2023-02-13T11:53:50+08:00

061. Characteristics and Classification of Choroidal Caverns in Patients with Various Retinal and Chorioretinal Diseasesyiqi.zhang2023-02-13T11:53:50+08:00

058. A Novel Mutation Located in the Intermembrane Space Domain of AFG3L2 Causes Dominant Optic Atrophy Through Decreasing the Stability of the Encoded Protein

yiqi.zhang2023-04-18T17:39:14+08:00

058. A Novel Mutation Located in the Intermembrane Space Domain of AFG3L2 Causes Dominant Optic Atrophy Through Decreasing the Stability of the Encoded Proteinyiqi.zhang2023-04-18T17:39:14+08:00

057. Genotypes and Phenotypes Analysis of a Novel Complex Heterozygous Mutation of CEP290 Related Isolated Cone-Rod Dystrophy

yiqi.zhang2023-04-18T17:42:13+08:00

057. Genotypes and Phenotypes Analysis of a Novel Complex Heterozygous Mutation of CEP290 Related Isolated Cone-Rod Dystrophyyiqi.zhang2023-04-18T17:42:13+08:00

055. Analysis of White and Dark without Pressure in a Young Myopic Group Based on Ultra-Wide Swept-Source Optical Coherence Tomography Angiography

yiqi.zhang2023-02-13T11:32:54+08:00

055. Analysis of White and Dark without Pressure in a Young Myopic Group Based on Ultra-Wide Swept-Source Optical Coherence Tomography Angiographyyiqi.zhang2023-02-13T11:32:54+08:00

054. Supernormal Rod Response Mediated by a Novel KCNV2 Variant in a Cone Dystrophy Type 3B Patient

yiqi.zhang2023-04-18T17:44:05+08:00

054. Supernormal Rod Response Mediated by a Novel KCNV2 Variant in a Cone Dystrophy Type 3B Patientyiqi.zhang2023-04-18T17:44:05+08:00