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The 13q14 Deletion in Retinoblastoma

Kim JW, Chung SK, Chung SM

  • KMID: 1949588
  • J Korean Ophthalmol Soc.
  • 1991 Dec;32(12):1076-1079.
Retinoblastoma is the most common intraocular malignant tumor in children. Retinoblastoma is divided two groups, hereditary and non-hereditary. Hereditary retinoblastoma is relakd to chormosomal abnormalities. By banding technique of somatic...
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Three Cases of Trilateral Retinoblastoma

Choi SW

  • KMID: 1979934
  • Korean J Pediatr Hematol Oncol.
  • 2000 Apr;7(1):141-145.
Retinoblastoma is the most common ocular malignancy in childhood. The association of bilateral retinoblastoma with ectopic midline intracranial tumor, trilateral retinoblastoma syndrome, is rare, but the prognosis is very...
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Four Families of Hereditary Retinoblastoma

Yu YS, Lee TW, Song JS

  • KMID: 2336599
  • J Korean Ophthalmol Soc.
  • 1996 Dec;37(12):2148-2152.
We analysed the clinical findings in four families of hereditary retinoblastoma. All four children with retinoblastoma were male. Two of them were diagnosed after two years of age and the...
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A Case of Retinoblastoma and Coats' Disease in the Same eye: A Clinicopathologic Report

Kim HK, Min IS, Cho HK

  • KMID: 2204724
  • J Korean Ophthalmol Soc.
  • 1982 Sep;23(3):793-797.
A case of retinoblastoma and Coats' disease in the same eye is presented. Coexisitence of the retinoblastoma and Coats' disease is very rarely seen, though the retinoblastoma or the Coats'...
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Bilateral Retinoblastoma in Identical Twins

Kim SH, Kim JB, Kim SM

  • KMID: 2107223
  • J Korean Ophthalmol Soc.
  • 1977 Mar;18(1):97-100.
We have experienced a rare case of bilateral retinoblastoma in identical twins recently. Their mother noticed that elder sister gazed upward when she fixated some object 5 days ago. On...
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Retinoblastoma Manifested by Hyphema and Orbital Cellulitis

Park SC, Chung SK, Baek NH

  • KMID: 2204964
  • J Korean Ophthalmol Soc.
  • 1991 Feb;32(2):180-183.
The authors experienced a case of retinoblastoma in a two-year-old female who had recurrent hyphema and marked erythematous lid swelling. We treated her for orbital cellulitis and hyphema, but those...
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Ultrasonography of a Case of Retinoblastoma

Jang JY, Cho KH, Oh JS

  • KMID: 2122595
  • J Korean Ophthalmol Soc.
  • 1980 Dec;21(4):609-612.
The authors experienced a case of retinoblastoma which occured in left eye of a 8 month old Korean male. We had a study of the ultrasonographic finding for a case...
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A Case of Osteosarcoma Developed in a Patient of Untreated Bilateral Retinoblastoma

Kim BH, Lee TW

  • KMID: 2123497
  • J Korean Ophthalmol Soc.
  • 1996 Aug;37(8):1298-1302.
Retinoblastoma is one of the primary malignant tumors which rarely undergo spontaneous regression. Survival rate from retinoblastoma is in excess of 90%, but the subsequent development of second tumor is...
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Retinoblastoma

Han HJ, Park BI

  • KMID: 2107005
  • J Korean Ophthalmol Soc.
  • 1970 Dec;11(4):59-65.
Retinoblastoma has been established as an inheritable disease. To the development of sporadic cases the mutation can be ascrivable. Once the gene has been established, however, it is transmitted as...
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CT findings of retinoblastoma

Byun WM, Jung KH, Cho KH, Kim SY, Hwang MS, Chang JC

Authors retrospectively analyzed CT findings of 10 cases which proved retinoblastoma by pathology from May in1983 to August in 1986 at Yeungnam University Hospital. The results obtained were as follows:...
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Retinoblastoma

Kim HM

  • KMID: 1611118
  • Korean J Pediatr.
  • 2004 Jun;47(Suppl 2):S447-S455.
No abstract available.
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Trilateral Retinoblastoma

Kim HS, Cho KG, Cho KH, Yoon SH, Ahn YM, Ahn YH, Shim C

  • KMID: 1904703
  • J Korean Neurosurg Soc.
  • 2001 May;30(5):647-651.
Trilateral retinoblastoma is a syndrome involving midline intracranial malignancies in children with the heritable form of retinoblastoma. It is rare and usually lethal in spite of aggressive treatments. We report...
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Metastatic Retinoblastoma to Tibia: A Case Report

Bae DH, Lim JK, Song JS

Retinoblastoma is a malignant tumor that arises from the retina. The prognosis is very unfavorable if the choroid is affected or the central nervous system is invaded or if metastasis...
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Clinical Characteristics of the Retinoblastoma Diagnosed before One Year Old

Yang JG, Yu YS

  • KMID: 2022636
  • J Korean Ophthalmol Soc.
  • 1996 Jun;37(6):1005-1011.
To evaluate the clinical characteristics of retinoblastoma diagnosed before one year old. 19 children with retinoblastoma were observed with clinical records, retrospectively. Thirteen patients had unilateral retinoblastoma. and 6 patients...
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Enzyme Histochemical Study of Retinoblastoma

Kweon EY, Cho NC

  • KMID: 2337087
  • J Korean Ophthalmol Soc.
  • 2003 Feb;44(2):454-458.
PURPOSE: The histiogenesis of retinoblastoma, the most common intraocular malignancy of childhood, has been investigated from the early times. But in spite of this effort, its origin has been controversial....
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Loss of the retinoblastoma gene in non-small cell lung cancer

Lee CT, Kim CM, Zo JI, Shim YM, Hong WS, Lee JO, Kang TW

  • KMID: 2049913
  • Tuberc Respir Dis.
  • 1993 Apr;40(2):98-103.
No abstract available.
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Current Assessment and Management of Retinoblastoma

Chueh HW

Retinoblastoma is the most common intraocular malignancy in childhood. Diagnosis is currently made by ophthalmologists under general anesthesia as it is the gold standard for intraocular assessment. However, evaluations for...
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A Case of Retinal Dysplasia with PHPV

Kim SY, Park JM

  • KMID: 2123362
  • J Korean Ophthalmol Soc.
  • 1995 May;36(5):885-889.
Retinal dysplasia is an abnormal differentiation of the retina at embryonal retina stage with proliferation of its elements into rosettes, fold, and gliosis and it is very difficulat to distinguish...
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A Case of Retinoblastoma Presenting With Dislocated lens

Lee HJ, Chung MR, Choi DG, Kim HK

  • KMID: 2337026
  • J Korean Ophthalmol Soc.
  • 2002 Jun;43(6):1091-1094.
PURPOSE: It has been known that retinoblastoma very rarely produces a dislocated lens. We report herein a case of retinoblastoma with a dislocated lens. METHODS: A 2-year-old boy developed left conjunctival...
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Deletion of Rb1 gene in late osteosarcoma from survivor of unilateral retinoblastoma: a case report

Lee SY, Jeon DG, Lee JS, Hwang CS, Huh K, Lee TW, Hong SI

It has been well known that the survivors of retinoblastoma are prone to have osteosarcoma. But the secondary tumor usually occurs in bilateral, hereditary type of retinoblastoma. We report one...
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