- Three Cases of Leber's Hereditary Optic Atrophy in One Family
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Park JC, Lee JH, Chang WU
- KMID: 1665776
- J Korean Ophthalmol Soc.
- 1980 Sep;21(3):361-365.
The authors have experienced with three cases of Leber's hereditary optic atrophy one family which is a relatively rare condition characterized by acute or subacute failrure of central vision presenting... -
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- A Case of Optic Atrophy following Methanol Poisoning
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Song MS, Yoon BJ
- KMID: 1949553
- J Korean Ophthalmol Soc.
- 1989 Dec;30(6):1021-1024.
Methanol poisoning is a rare disease but may cause blindness and, in severe cases, results in death. It may develop lesions in optic nerve and retina, which may be accompanied... -
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- Visual Rehabilitation of Optic Atrophy Patients with Low Vision Aids
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Kim JW, Chang SI, Moon NJ
- KMID: 2336618
- J Korean Ophthalmol Soc.
- 1997 Mar;38(3):450-457.
In oder to evaluate the efficacy of low vision aids in patients with optic atrophy, we analyzed sex, age distribution, preexisting conditions, visual acuities before and after low vision aids... -
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- The Etiology of Optic Neuropathy
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Hwang JM, Jung YC
- KMID: 2336840
- J Korean Ophthalmol Soc.
- 1999 Apr;40(4):1078-1083.
In order to investigate causative mechanisms of optic neuropathy, retrospective clinical studies including ophthalmologic examination, imaging study, and molecular biologic analyses were performed on 322 patients with optic neuropathy. The... -
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- Clinical Survey of 110 Cases of Optic Atrophy
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Lee OH, Koo BS, Kwon KT
- KMID: 1948673
- J Korean Ophthalmol Soc.
- 1963 Jan;4(1):39-43.
1. 110 cases of optic atrophy from 7 months to 67 years old, 82 bilateral with 28 unilateral involvement observed at the National Medical Center in Korea Between 1959 and... -
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- Visual Deterioration in Osteopetrosis Reversed by Early Optic Nerve Decompression
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Hwang JM, Kim IO, Wang KC
- KMID: 2205654
- J Korean Ophthalmol Soc.
- 1999 Nov;40(11):3161-3167.
Visual loss with optic atrophy is common in osteopetrosis. An 8-year-old girl with osteopetrosis showed visual deterioration presumed to be related with compressive optic neuropathy. Her grandfather, uncle on mother's... -
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- Septo-optic dysplasia plus diagnosed in a middle-aged woman
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Oh ST, Kang MR, Oh SI, Kim EG, Kim SJ, Seo JH, Chung EJ, Ji KH
- KMID: 2454710
- Ann Clin Neurophysiol.
- 2018 Jul;20(2):85-88.
- doi: 10.14253/acn.2018.20.2.85
Septo-optic dysplasia is a congenital anomaly with diverse phenotypes from normal to mixtures of visual abnormality, endocrine dysfunction, psychomotor retardations and epileptic seizures. It is characterized by optic atrophy, pituitary... -
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- Leber's Hereditary Optic Neuropathy in Two Brothers of a Family
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Hur J, Sohn HY, Won IG
- KMID: 2122947
- J Korean Ophthalmol Soc.
- 1990 Feb;31(2):241-248.
The Leber's hereditary optic neuropathy, which affects mainly males in the late teens or in the early twenties, is a rare inherited disorder characterized by bilateral rapid loss of central... -
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- Two Cases of Leber's Hereditary Optic Atrophy Occurred in Mother and Son
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Park BG, Kim KS
- KMID: 2204736
- J Korean Ophthalmol Soc.
- 1982 Sep;23(3):867-871.
Leber's hereditary optic atrophy is characterized by sudden loss of central vision occuringin the second and third decade of life and nondirect transmission with male preponderance, Leber disease affecting both... -
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- A Mitochondrial Mutation in Leber's Hereditary Optic Neuropathy
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Hwang JM, Park HW
- KMID: 2205183
- J Korean Ophthalmol Soc.
- 1995 Dec;36(12):2218-2224.
Leber's hereditary optic neuropathy is caused by a single nucleotide change in the mitochondrial deoxynucleic acid(mtDNA). We identified a single guanine to adenine transition mutation in the mitochondrial DNA at... -
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- Clinical Manifestations of Leber's Hereditary Optic Neuropathy with 11778 mtDNA Mutation
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Kim SJ, Hwang JM, Park HW
- KMID: 2123512
- J Korean Ophthalmol Soc.
- 1996 Aug;37(8):1389-1396.
Leber's hereditary optic neuropathy is caused by a single nucleotide change in the mitochondrial deoxynucleic acid(mtDNA) and accounts for 30% of bilateral optic atrophy of unknown etiology. The authors found... -
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- Letter to the Editor: A Case of Optic Nerve Atrophy with Severe Disc Cupping after Methanol Poisoning
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Sanaei-Zadeh H, Zamani N
- KMID: 1031198
- Korean J Ophthalmol.
- 2011 Dec;25(6):463-463.
- doi: 10.3341/kjo.2011.25.6.463
No abstract available. -
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- Evaluation of clinically applied visual evoked potential (VEP) in ophthalmological and neurological diseases
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Kwak HW, Kim SM
- KMID: 1734996
- Korean J Ophthalmol.
- 1987 Jun;1(1):26-30.
- doi: 10.3341/kjo.1987.1.1.26
VEPs weie recorded in 222 cases of different disease groups and in 42cases of the control group using a Nicolet CA 1000 system. The latency time of N1, P1, N2,... -
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- A Case of Foster Kennedy Syndrome
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Jang WB, Park SH, Shin H
- KMID: 2123364
- J Korean Ophthalmol Soc.
- 1995 May;36(5):890-900.
The Foster Kennedy syndrome is ipsilateral optic disc atrophy and contralateral optic disc edema that is caused not only frontal lobe tumor but also another intracranial tumors and non tumorous... -
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- Optic Neuritis and Optic Atrophy
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Oum BS
- KMID: 2122764
- J Korean Ophthalmol Soc.
- 1987 Aug;28(4):909-915.
Optic neuritis is general term used to describe involvement of the optic nerve as a result of inflammation, demyelination, or infection. Other disorders of the optic nerves, including those of... -
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- Foster-Kennedy Syndrome
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Koo KI
- KMID: 1948552
- J Korean Ophthalmol Soc.
- 1972 Jun;13(2):87-88.
We reported one case of male, aged 42 years who was first seen on September 23, '71. His visual acuity were no light perception. Funduscopic examination showed optic atrophy in... -
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- A Study of Pattern Reversal Visual Evoked Potential and Flash Electroretinogram in Patients with Optic Atrophy
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Hong SU, Kim DH, Choi MS, Park KH, Kim SW
- KMID: 2184378
- J Korean Neurol Assoc.
- 1989 Jun;7(1):35-41.
The pattern reversal visual evoked potential(PRVEP) and flash electroretinogram(flash ERG) were performed in 22 patients with optic atrophy. Patients with ophthalmologic problems other than optic atrophy or with systemic disorders... -
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- A Case of Leber Hereditary Optic Neuropathy Showing Optic Disc Hyperfluorescence
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Park YJ, Lim HT
- KMID: 2431847
- J Korean Ophthalmol Soc.
- 2019 Jan;60(1):96-101.
- doi: 10.3341/jkos.2019.60.1.96
PURPOSE: We report an unusual case of Leber hereditary optic neuropathy presenting with optic disc hyperfluorescence. CASE SUMMARY: A 17-year-old male with sequential painless visual loss 3 weeks apart affecting first... -
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- A Case of Osteopetrosis with Optic Atrophy
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Roh YB, Cho KR, Jo KI, Jo YH, Lee SH, Pak BG
- KMID: 2122599
- J Korean Ophthalmol Soc.
- 1980 Dec;21(4):633-635.
The authors experienced a case of osteopetrosis with optic atrophies and nystagmoid movements, exceedingly rare disease, in 12 year-old girl for 5 years without fracture in long bone. On the... -
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- Leber's Hereditary Optic Neuropathy with Olivocerebellar Degeneration due to G11778A and T3394C Mutations in the Mitochondrial DNA
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Nakaso K, Adachi Y, Fusayasu E, Doi K, Imamura K, Yasui K, Nakashima
- KMID: 2287596
- J Clin Neurol.
- 2012 Sep;8(3):230-234.
- doi: 10.3988/jcn.2012.8.3.230
BACKGROUND: Leber's hereditary optic neuropathy (LHON) is a mitochondrial disorder with optic nerve atrophy. Although there are no other associated neurological abnormalities in most cases of LHON, cases of "LHON... -
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