Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

138 results
Display

Ultrasonography of polycystic kidney

Oh SC, Cho SG, Kim KS, Lee KS

Polycystic diseases is defined as a heritable disorder with diffuse involvement of both kidneys. The term"Polycystic disease"comprises at least two separate, genetically different diseases-one with an onset typically inchildhood (infantile...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Three Cases of Polycystic Kidney

Kim HS, Lee HS

  • KMID: 1911053
  • Korean J Urol.
  • 1961 Apr;2(1):125-127.
Three cases of polycystic kidney were treated with conservative therapy. Of three cases one showed normal blood pressure and improved digestive disturbance after the therapy. i. e., direct aspiration of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Transitional Cell Carcinoma Associated with Adult Polycystic Kidney Disease

Yea SH, Jeong YB, Jeong DH, Kim JH, Park YI, Jo SY

  • KMID: 1914392
  • Korean J Urol.
  • 1997 Aug;38(8):877-881.
Some cases of renal malignancy associated with adult (autosomal dominant) polycystic kidney disease have been reported. Most of these malignancies were diagnosed as renal cell carcinoma. But the case of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Segmental Cystic Disease of the Kidney: A Case Report

Han SB, Chung SH, Cho JH

Segmental cystic disease of the kidney is a rare form of cystic disease of the kidney that manifests as variable sized, numerous cysts that are localized in a segment of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Infantile Polycystic Kidney

Ko IY, Jung CH, Song JB, Seo KY, Shim JS

  • KMID: 2269888
  • Korean J Obstet Gynecol.
  • 1999 Sep;42(9):2115-2117.
The infantile polycystic kidney disease is rare fetal urinary tract anomaly. It is inherited with an autosomal recessive pattern and recurrence rate is 25%. The gene locus is on...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Prenatal Diagnosed Polycystic Kidney

Kang BY, Baek JW, Choi SU, Lee JH, Kim JI

  • KMID: 2072350
  • Korean J Perinatol.
  • 2002 Mar;13(1):52-55.
The infantile polycystic kidney disease is rare urinary tract anomaly.It is inherited with an autosomal recessive pattern and recurrence rate is about 25%. The gene locus is on chromosome 6p....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of bilateral polycystic kidney: prenatal ultrasonographic diagnosis

Seo JW

  • KMID: 1696803
  • Korean J Obstet Gynecol.
  • 1991 Nov;34(11):1625-1629.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Recurrent Fetal Cystic Hygroma with Polycystic Kidney

Kim SH, Sin JW, Kim HJ, Seo SS, Ha HM

  • KMID: 2075291
  • Korean J Obstet Gynecol.
  • 1997 Aug;40(8):1756-1762.
This is a case report of a cystic hygroma with polycystic kidney in a fetus which was suspected by ultrasonography and was confirmed by autopsy. Recently, we have experienced this...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of prenatally diagnosed fetal unilateral multicystic dysplastic kidney with contralateral autosomal recessive polycystic kidney

Kim SY, Lee HW, Jung E

  • KMID: 2273250
  • Korean J Obstet Gynecol.
  • 2008 Feb;51(2):236-240.
Multicystic dysplastic kidney (MCDK) is an incidental finding on prenatal ultrasound examination and this abnormality may be unilateral or bilateral. In approximately 20-50 % of case, there are also abnormalities...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Autosomal Dominant Polycystic Kidney Desease Coexisting with Renal Dysplasia. First Case Described and Followed Since Prenatal Period

Truyols C

Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent hereditary renal disease and causes terminal chronic renal failure. ADPKD is characterized by bilateral multiple renal cysts, which are produced...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Renal Cell Carcinoma in Autosomal Dominant Polycystic Kidney Disease Hemodialyzed

Hur SH, Song KS, Park JW, Shin SK, Kang DO, Kim JH, Koo JH, Kim SR

  • KMID: 2307322
  • Korean J Nephrol.
  • 1999 Sep;18(5):836-840.
The development of renal cell carcinoma in auto-sornal dominant polycystic kidney disease hemodialyzed was rarely found. A sixty-six year old man has been hemodialyzed for four years. His end-stage renal...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Prenatal Ultrasonographic Findings of Renal Cystic Diseases of the Fetus

Cho JY, Song MJ, Lee YH, Cho BJ, Hong SR

  • KMID: 1616717
  • J Korean Soc Med Ultrasound.
  • 2002 Mar;21(1):39-45.
The renal cystic diseases of the fetus consist of variable types of multicystic dysplastic kidney, autosomal reces-sive polycystic kidney, autosomal dominant polycystic kidney, obstructive cystic renal dysplasia, simple renal cyst,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Spontaneous Rupture of the Autosomal Dominant Polycystic Kidney associated with Ureteral Calculi

Kim HW, Suh HJ, Lee DH, Lee JH

  • KMID: 2289948
  • Korean J Urol.
  • 1999 Apr;40(4):520-522.
Spontaneous rupture of the kidney is a relatively uncommon disease. It occurs secondary to various kinds of underlying disease such as infection, hydronephrosis, calculous disease, benign or malignant tumor, renal...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of Infantile Polycystic kidney

Kim AS, Park SB, Kim YG, Cho KH, Kim JS

  • KMID: 1676143
  • J Korean Pediatr Soc.
  • 1985 Feb;28(2):191-196.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Polycystic Kidneys: Report of 2 Cases

Kim DH, Choi IY, Song SI, Choi JH, Lee JB

  • KMID: 1677908
  • Korean J Urol.
  • 1978 Jun;19(3):247-251.
Polycystic kidneys are congenital and bilateral diseases, and those symptoms almost do not appear until after age 40. Two cases of polycystic kidneys in a 53 year-old male having suffered...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Autosomal Recessive Polycystic Kidney Disease Confirmed to PKHD1 Gene Mutation: A Case of PKHD1 Gene Mutation

Baek JE, Lee SM, Eun HS, Park MS, Park KI, Namgung R, Lee C

  • KMID: 2312960
  • Neonatal Med.
  • 2014 Feb;21(1):64-68.
Autosomal recessive polycystic kidney disease (ARPKD) is a severe form of polycystic kidney disease that is characterized by enlarged kidneys and congenital hepatic fibrosis. The clinical spectrum of this condition...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of tuberous Sclerosis with Polycystic Kidney

Lee WI, Moon IS, Lee PM, Lee JC

  • KMID: 1668578
  • J Korean Pediatr Soc.
  • 1981 Nov;24(11):1100-1105.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Polycystic Kidney Disease Presenting as Subarachnoid Hemorrhage Due to Ruptured Cerebral Aneurysm: An Autopsy Case

Choi YD, Lee HY, Kim YS

  • KMID: 1593790
  • Korean J Pathol.
  • 2006 Dec;40(6):469-471.
Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disorder characterized by multiple expanding cysts in both kidneys, and they ultimately destroy the renal parenchyma and cause renal failure. Intracranial...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Renal Cell Carcinoma in Adult Polycystic Kidney Disease: A Case Report

Lee HJ, Cho JH

  • KMID: 2117319
  • J Korean Radiol Soc.
  • 1997 Apr;36(4):683-685.
The authors report a case of a renal cell carcinoma occurring in an adult suffering from polycystic kidney disease and diagnosed by radiologic examination. The patient presented with palpable flank...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of consencutive infantile polycystic kidney in one nulliparous woman prenatal ultrasonographic diagnosis

Chung TI, Park SC, Lee MJ, Kim JI, Kim TH

  • KMID: 1691473
  • Korean J Perinatol.
  • 1993 Mar;4(1):87-93.
No abstract available.
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