Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

43 results
Display

A Case of Cystine Stone

Yoon DK, Shin YS, Koh SK

  • KMID: 2289654
  • Korean J Urol.
  • 1984 Feb;25(1):112-116.
Urinary tract calculi composed primarily of cystine are rare in adults and children. These are usually pure and found exclusively in patients with cystinuria. Cystinuria is an inherited defect in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
The Healing Effect of Keratocyne(R) on Corneal Diseases

Yang SW, Lee J

  • KMID: 1949367
  • J Korean Ophthalmol Soc.
  • 1988 Aug;29(4):517-520.
Keratocyne(R) is the complex of cystine and vitamine B6. Cystine is collagenase inhibitor and vitamine B6 is essential to the metabolism of cystine. We administered Keratocyne(R) orally combined with specific...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Cystine Stone in a Child

Cho CH, Hahm KS, Park JK, Kim KH

  • KMID: 2139657
  • Korean J Urol.
  • 1986 Dec;27(6):933-938.
Cystinuria is an autosomal recessive inherited defect in renal tubular reabsorption of four amino acids, cystine, ornithine, lysine and arginine. Homozygotes were identified by the formation of urinary tract calculi...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Cystine Stone : Report of Two Cases

Hah ST, Yoon JH, Yoon JB

  • KMID: 1911340
  • Korean J Urol.
  • 1981 Aug;22(4):451-455.
We herein report 2 cases of patient with urinary cystine stones. One was a 32-year-old woman and the other was a 52-year-old man. Each patient was found to have cystine...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Cystine Crystal Depositions within Cornea in Cystinosis

Choi YJ, Yoo JR, Park MR, Chung SK

  • KMID: 2125585
  • J Korean Ophthalmol Soc.
  • 2003 Jul;44(7):1689-1692.
PURPOSE: We report a case of systemic cystinosis who showed cystine crystal depositions within cornea. METHODS: A 13-year-old boy with systemic cystinosis who had chronic renal failure, growth retardation, rickets...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Anuria in a 9-Month-Old Infant Resulting from Ureteral Cystine Stones

Aboutaleb

  • KMID: 2315431
  • Korean J Urol.
  • 2011 Sep;52(9):647-649.
Pediatric urolithiasis and calcular anuria in early infancy are rare. Cystine stones may develop in utero or during early infancy. We report the case of a female 9-month-old infant with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Cystinosis

Jung MH, Keun SO, Lee SJ, Lee BC

  • KMID: 1606831
  • J Korean Pediatr Soc.
  • 2003 Jun;46(6):615-619.
Cystinosis, an autosomal recessively inherited lysosomal storage disease, results from impaired transport of the amino acid cystine out of cellular lysosomes. The consequent accumulation and crystallization of cystine destroys tissues,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Endocrine complications during and after adolescence in a patient with cystinosis

Ahn MB, Kim SE, Cho WK, Jung MH, Suh BK

Cystinosis is a rare disease characterized by abnormal lysosomal cystine accumulation of cystine due to impaired lysosomal transport. We previously reported the first case of cystinosis in Korea in a...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Pulmonary Thromboembolism Caused by PROS1 Gene Mutation

Jin SC

Pulmonary embolism (PE) is a serious clinical problem in patients with acquired risk factor such as cancer, immobilization, recent trauma and surgery. However PE may occur in hereditary thrombophilia like...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Homocystinuria with Ectopia Lentis

Chung DY, Chung YT

  • KMID: 2122983
  • J Korean Ophthalmol Soc.
  • 1991 Jan;32(1):110-115.
Homocystinuria is an inborn error on the pathway of the methionine metabolism. It is mainly caused by a cystathionine B-synthase deficiency in the brain or liver. Homocystinuria is biochemically characterized...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Multimodal Treatments of Cystine Stones: An Observational, Retrospective Single-Center Analysis of 14 Cases

Shim M, Park HK

PURPOSE: To document the experiences of a single institution in evaluating the clinical courses and treatment outcomes of patients with cystine stones. MATERIALS AND METHODS: The clinical data of 14 patients...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Analysis of the Urinary Stone Components Using Chemical Analysis Method

Byeon SS, Kim HH, Kim SW

  • KMID: 1913771
  • Korean J Urol.
  • 1996 Feb;37(2):179-186.
We analyzed the composition of urinary stones using chemical analysis method. From 1985 to 1995, 495 urinary calculi were eligible for stone analysis. Forty six per cent of the stones...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Trichothiodystrophy with a Low Sulfur Level in the Hair Shafts

Kim S, Park S, Im M, Seo Y, Lee J, Lee Y

  • KMID: 2146307
  • Korean J Dermatol.
  • 2011 Jan;49(1):36-39.
Trichothiodystrophy is a rare autosomal recessive disorder and it is caused by reduced levels of high-sulfur amino acids and most particularly cystine in hair shafts. The patients with trichothiodystrophy show...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Cystinuria with Multiple Renal Stones in an 8-month-old Girl

Kang EG, Lee JH, Lee BH, Kim GH, Park YS

  • KMID: 2098920
  • J Korean Soc Pediatr Nephrol.
  • 2013 Oct;17(2):122-126.
Cystinuria is an autosomal recessive disease characterized by impaired transport of cystine and dibasic amino acids in the proximal renal tubule, resulting in the formation of cystine stones. It is...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Non-Type I Cystinuria Associated with Mental retardation and Ataxia in a Korean Boy with a New Missence Mutation(G173R) in the SLC7A9 Gene

Lee EH, Kim YH, Hwang JS, Kim SH

Cystinuria is an inherited renal and intestinal disease characterized by defective amino acids reabsorption and cystine urolithiasis. It is unusually associated with neurologic symptoms. Mutations in two genes, SLC3A1 and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Clinical Observation on Analysis of Urinary Stones

Kim HS, Min BK

  • KMID: 2289551
  • Korean J Urol.
  • 1988 Feb;29(1):67-76.
The exact analysis of urinary stones is very important to the study of the etiology of stone formation, prevention of recurrence and medical treatment. We Have analyzed 260 urinary stones...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Analysis of Urinary Stone Components during the Last Two Decades

Ye SJ, Yoo ES, Park YK

PURPOSE: The accurate analysis of urinary stone components is fundamental for studying of the etiology of stone formation and it is essential for the treatment of urinary stone and its...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Effect of Therasonic Lithotripter LT-1000 for Urinary Tract Calculi in Children

Seo YJ, Chung SK, Park YK

  • KMID: 1914092
  • Korean J Urol.
  • 1996 Oct;37(10):1137-1141.
The treatment of urolithiasis in children has been changed dramatically by extracorporeal shock wave lithotripsy (ESWL) and endourological procedure in recent years. Especially, the use of extracorporeal shock wave lithotripsy...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Cystinuria 3 Cases

Choi JE, Yun BY, Park HW, Park JH, Ha IS, Jeong HI, Choi Y, Choi H, Kim IW

  • KMID: 2208341
  • J Korean Pediatr Soc.
  • 1995 Feb;38(2):245-251.
We report three cases of cystinuria, presenting with urinary stones. A 2-year-old girl presented with urinary difficulty, hematuria, dysuria of sudden onset, and her 7-month-old younger brother also was presented...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Spectroscopic Studies of Urinary Stone

Ahn OC

  • KMID: 1677537
  • Korean J Urol.
  • 1973 Sep;14(3):165-172.
Although there are a number of literature on the chemical composition of urinary stones, problems of the urolithiasis, particularly concerning [the pathogenesis of stone formation, are yet to be solved....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr