1 原理和方法Principles and Methods 1．1 全視野視網膜電圖(Full—Field Electroretinograms) 1．2 黃斑局部ERG(Focal Macular ERG) 1．3 多焦ERG(Multifocal ERG) 1．4 眼電圖(EIectrooculography) 1．5 光學相乾斷層掃描(OCT)(Optical Coherence Tomography)2 遺傳性視網膜病變及相關疾病Hereditary Retinal and Allied Diseases 2．1 視網膜色素變性(Retinitis Pigmentosa) 2．2 結晶樣視網膜病變(Crystalline Retinopathy，Bietti) 2．3 Batten病(Batten Disease) 2．4 卡恩斯-塞爾綜閤徵(Kearns—Sayre Syndrome) 2．5 無脈絡膜癥(Choroideremia) 2．6 迴鏇狀萎縮(Gyrate Atrophy) 2．7 增強藍錐細胞綜閤徵(Enhanced S-cone Synd rome) 2．8 X-連鎖視網膜劈裂(X-linked Retinoschisis) 2．9 Nettleship—Falls 2(連鎖眼白化病(Nettleship—Falls X-Linked Ocular Albinism) 2．10 完全型和不完全型先天性靜止性夜盲(Complete and Incomplete Types of CSNB) 2．11 白點狀眼底(Fundus AIbipunctatus) 2．12 小13病(Oguchi’S Disease) 2．13 視錐細胞營養不良(Cone Dystrophy) 2．14 視杆細胞單色視(Rod Monoch romacy) 2．15 藍錐細胞單色視(Blue Cone Monoch romacy) 2．16 先天性藍色盲與顯性遺傳性青少年視神經萎縮的鑒彆診斷(Congenital Tritanopia-Differential Diagnosis of Dominantly Inherited Juvenile Optic Atrophy) 2．17 視杆-視錐細胞功能障礙綜閤徵伴不常見的ERG錶現類型(Rod—Cone Dysfunction Syndrome with an Unusual Form of ERG) 2．18 負波形ERG與不明原因病變的關係(Association of Negative ERG with Diseases of Unknown Etiology) 2．19 隱匿性黃斑營養不良(Occult Macular Dystrophy) 2．20 Stargardt’S病(眼底黃色斑點癥)(Stargardt’S Disease，Fundus flavimaculatus) 2．21 Best’S病(Best’S Disease)3 獲得性視網膜疾病Acquired Retinal Diseases 3．1 糖尿病視網膜病變(Diabetic Retinopathy) 3．2 視網膜循環障礙(Retinal Circulatory Disturbances) 3．3 視網膜及脈絡膜脫離(Retinal and Choroidal Detachment) 3．4 視網膜及脈絡膜炎癥性疾病(Inflammatory Diseases of Retina and Choroid)4 獲得性黃斑疾病Acquired Macular Diseases 4．1 中心性漿液性脈絡膜視網膜病變(Central Serous Chorioretinopathy) 4．2 無晶體眼或人工晶體眼黃斑囊樣水腫(Aphakic or Pseudophakic Cystoid Macular Edema) 4．3 特發性黃斑前膜(Idiopathic Epimacular Membranes) 4．4 中心凹厚度與黃斑局部ERG(Foveal Thickness and Focal Macular ERG) 4．5 特發性黃斑裂孔(Idiopathic Macular Hole) 4．6 黃斑假孔(Macular Pseudohole) 4．7 年齡相關性黃斑變性(Age—Relafed Macular Degeneration)索引(Subject Index)
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