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Two Cases of Hereditary Crystalline Corneal Dystrophy of Schnyder

Kim HB, Kong YT, Hong YJ

  • KMID: 2107046
  • J Korean Ophthalmol Soc.
  • 1973 Dec;14(4):387-391.
The authors present a family with two members affected by hereditary corneal dystrophy of Schnyder. A 45-year-old mother and her 15-year-old son visited our hospital with bilateral opacities which affected...
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N102S Mutation of UBIAD1 Gene in a Family with Schnyder Crystalline Corneal Dystrophy

Chung WS, Hong HK, Kim TI, Kim EJ, Kim EK

  • KMID: 2337820
  • J Korean Ophthalmol Soc.
  • 2010 Mar;51(3):440-446.
PURPOSE: Schnyder crystalline corneal dystrophy (SCCD) is an autosomal dominant disease characterized by progressive central corneal opacification and premature development of peripheral arcus in the cornea. This disease results from...
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Clinical Manifestations of Avellino Corneal Dystrophy Diagnosed by Non-invasive Genetic Test

Kim JW, Kim HM, Song JS

  • KMID: 2337659
  • J Korean Ophthalmol Soc.
  • 2008 Sep;49(9):1431-1436.
PURPOSE: To introduce a new genetic method for the diagnosis of Avellino corneal dystrophy (ACD), which is non-invasive and can be easily performed on an outpatient basis, and to evaluate...
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Lattice Corneal Dystrophy, Gelsolin Type: The First Case Report in Korea

Kim TH, Bae JH, Lim DH, Chung ES, Chung TY

PURPOSE: To report the first case of lattice corneal dystrophy, gelsolin type in Korea. CASE SUMMARY: A 61-year-old man visited our clinic with severe dry eye symptom in both eyes. Clinical...
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The Number of Cases, Cause and Treatment of Avellino Corneal Dystrophy Exacerbated After LASIK

Yi JH, Ha BJ, Kim SW, Kim TI, Kim EK

  • KMID: 2337657
  • J Korean Ophthalmol Soc.
  • 2008 Sep;49(9):1415-1424.
PURPOSE: To present a case report of fungal keratitis related to prolonged overnight use of orthokeratology contact lenses. METHODS: A 13 year-old girl presented with a corneal ulcer in her left...
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A Case of Korean Patient with Macular Corneal Dystrophy Associated with Novel Mutation in the CHST6 Gene

Lee YK, Chang DJ, Chung SK

To report a novel mutation within the CHST6 gene, as well as describe light and electron microscopic features of a case of macular corneal dystrophy. A 59-year old woman with...
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Visual Outcomes Following Deep Anterior Lamellar Keratoplasty in Granular Corneal Dystrophy Types 1 and 2

uit de Bosch LM, Ormonde S, Misra SL

No abstract available.
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A Korean Patient with Lattice Corneal Dystrophy Type IV with Leu527Arg Mutation in the TGFBI Gene

Kim J, Lee KA, Kim EK, Lee HK

An 87-year-old woman visited our clinic for a scheduled cataract surgery. At the time of preoperative evaluation, slit lamp examination showed lattice-shaped and granular deposits with asymmetrical patterns in the...
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Confocal Microscopic Findings in Posterior Polymorphous Corneal Dystrophy

Choi BS, Park YM, Lee JS

PURPOSE: To analyze the features of corneal tissue in patients with posterior polymorphous corneal dystrophy (PPMD) using in vivo confocal microscopy (IVCM). CASE SUMMARY: Three patients with clinically diagnosed PPMD were...
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A Novel Decorin Gene Mutation in Congenital Hereditary Stromal Dystrophy: A Korean Family

Lee JH, Ki CS, Chung ES, Chung TY

A 43-year-old man developed decreased vision in the right eye that had persisted for seven years. Under slit lamp examination, corneal clouding was noted with normal endothelium and ocular structure....
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The Effects of the Cyanoacrylate Tissue Adhesive Mono-therapy for Corneal Perforation

Koh JW, Cho HH, Yang SW, Her J

  • KMID: 2110341
  • J Korean Ophthalmol Soc.
  • 2006 Sep;47(9):1381-1386.
PURPOSE: To report cases of corneal perforation among corneas treated with cyanoacrylate tissue adhesive. METHODS: We performed cyanoacrylate tissue adhesive application on 1 case of corneal perforation due to fungal...
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Current Status of Primary Glomerulonephritis

Chae DW

  • KMID: 2267899
  • Korean J Med.
  • 2013 Jan;84(1):1-5.
Recent change in major indication for renal biopsy from nephrotic syndrome to asymptomatic urinary abnormality (AU) in Korea makes IgA nephropathy the most common biopsy-confirmed glomerulonephritis (GN). Beside from the...
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A case of Castleman's disease patient treated successfully with cyclic high-dose steroid therapy

Cho SW, Chung HJ, Kim SH, Choi JS, Kang GH, Oh HS

  • KMID: 2081817
  • Korean J Med.
  • 2010 Jul;79(1):72-76.
Castleman's disease is rare, and its cause is unknown. Although various treatments have been attempted, no standard treatment has been established for it. A 51-year-old male on hemodialysis with end-stage...
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Mutation Analysis of the TGFBI Gene in Consecutive Korean Patients With Corneal Dystrophies

Song JS, Lim DH, Chung ES, Chung TY, Ki CS

BACKGROUND: Mutations in the transforming growth factor beta-induced gene (TGFBI) are major causes of genetic corneal dystrophies (CDs), which can be grouped into TGFBI CDs. Although a few studies have...
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Genome-wide scan of granular corneal dystrophy, type II: confirmation of chromosome 5q31 and identification of new co-segregated loci on chromosome 3q26.3

Lee EJ, Kim KJ, Kim HN, Bok J, Jung SC, Kim EK, Lee JY, Kim HL

Granular corneal dystrophy, type II (CGD2; Avellino corneal dystrophy) is the most common corneal dystrophy among Koreans, but its pathophysiology is still poorly understood. Many reports showed that even though...
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Therapeutic response of cyclosporine and outcome in steroid resistant nephrotic syndrome

Choi HS, Lee JH, Park YS

PURPOSE: The aim of our study was to evaluate the therapeutic response to cyclosporine, time to remission and side effects in steroid resistant nephrotic syndrome (SRNS). METHODS: This study included 22...
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A Case of Nephrotic Syndrome after Thymectomy due to Thymoma

Kim KM, Kim HW, Sun BJ, Sohn BS, Chung YH, Lee PH, Park HJ, Park IS, Cho YM, Park SK

  • KMID: 2253234
  • Korean J Nephrol.
  • 2008 Jul;27(4):492-496.
Thymoma is often accompanied by different paraneoplastic syndrome, such as myasthenia gravis, pure red-cell aplasia, systemic lupus erythematosus. Association of glomerulonephritis and thymic tumor is very rare, with only about...
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C1q Nephropathy: A Distinct Pathologic Entity

Shin JH, Kim TE, Lee KY, Shim SI, Choi YJ

  • KMID: 2459593
  • Korean J Pathol.
  • 2009 Aug;43(4):335-341.
BACKGROUND: C1q nephropathy (C1qN) is a controversial diagnostic entity defined by Jennette and Hipp in 1985. The prevalence is very low and a few large scale studies have been reported....
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Urinary Angiotensinogen Excretion and Intrarenal Angiotensinogen Expression in Minimal Change Disease Patients

Jang HR, Jo A, Park JH, Lee JE, Huh W, Kim DJ, Oh HY, Kim YG

  • KMID: 2141999
  • Korean J Nephrol.
  • 2011 Nov;30(6):593-600.
PURPOSE: Urinary angiotensinogen (AGT) has been reported as an important marker reflecting the activity of intrarenal renin-angiotensin system (RAS) in chronic glomerulonephritis patients. We investigated urinary AGT excretion and intrarenal...
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Changes in Spherical Aberration after Various Corneal Surface Ablation Techniques

Ahn HS, Chung JL, Kim EK, Seo KY, Kim TI

PURPOSE: The corneal change induced by refractive procedures influence both the postoperative refractive status and the ocular spherical aberration (SA). We evaluated changes in corneal SA after three types of...
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