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1. 視神経の先天性および後天性異常 congenital anomalies and acquired abnormalities of the optic nerve
2. 非動脈炎性前部虚血性視神経症：臨床的特徴および診断 nonarteritic anterior ischemic optic neuropathy clinical features and diagnosis
3. 成人における片頭痛の病態生理、臨床症状、および診断 pathophysiology clinical manifestations and diagnosis of migraine in adults
4. 網膜色素変性症：臨床症状および診断 retinitis pigmentosa clinical presentation and diagnosis
5. 腫瘍随伴性視覚症候群 paraneoplastic visual syndromes

Schilimow A1, Wiechens B.
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft.Ophthalmologe.2015 Jul 4. [Epub ahead of print]
CASE REPORT: A 29-year-old female patient presented with a unilateral deterioration of visual acuity, metamorphopsia and a paracentral scotoma. The patient had suffered from a viral rhinitis 1 week prior to the ophthalmological symptoms.DIAGNOSTICS: Fundoscopy revealed parafoveal changes in the reti
PMID 26142230

Smirnov V1, Drumare I, Bouacha I, Puech B, Defoort-Dhellemmes S.
Documenta ophthalmologica. Advances in ophthalmology.Doc Ophthalmol.2015 Jul 3. [Epub ahead of print]
INTRODUCTION: Oligocone trichromacy (OT) is an uncommon cone dysfunction disorder, the mechanism of which remains poorly understood. OT has been thought to be non-progressive, but its long-term visual outcome has been seldom reported in the literature. Our aim was to present two OT patients followed
PMID 26138751

Choroidal neovascularisation as an unusual ophthalmic manifestation of cat-scratch disease in an 8-year-old girl.

Latanza L1, Viscogliosi F, Solimeo A, Calabrò F, De Angelis V, De Rosa P.
International ophthalmology.Int Ophthalmol.2015 Jul 2. [Epub ahead of print]
To report the first case of choroidal neovascularisation (CNV) that appeared during the primary Bartonella henselae infection in an 8-year-old girl. An 8-year-old girl was referred to our clinic complaining of a central scotoma in the right eye. Fundus examination revealed a bilateral disc oedema an
PMID 26135983

Moyamoya Syndrome Associated With Gamma Knife Surgery for Cerebral Arteriovenous Malformation : Case Report