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Three Cases of Leber's Hereditary Optic Atrophy in One Family

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

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

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

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

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

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

Oh ST, Kang MR, Oh SI, Kim EG, Kim SJ, Seo JH, Chung EJ, Ji KH

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

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

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

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

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

Sanaei-Zadeh H, Zamani N

No abstract available.
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Evaluation of clinically applied visual evoked potential (VEP) in ophthalmological and neurological diseases

Kwak HW, Kim SM

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

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

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

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

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

Park YJ, Lim HT

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

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

Nakaso K, Adachi Y, Fusayasu E, Doi K, Imamura K, Yasui K, Nakashima

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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