Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

PUBLICATION DATE

12 results
Display

A Case of Secondary FSGS due to Chronic Chloride Diarrhea

Kim BK, Lee HS, Yim HE, Cheong HI, Yoo KH

Congenital chloride diarrhea (CLD) is a rare autosomal recessive disease that is difficult to diagnose. CLD requires early treatment to correct electrolyte imbalance and alkalosis and to prevent severe dehydration....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Unilateral noncystic renal dysplasia in a Sprague Dawley rat

Lee YH, Kim D, Park SH, Lee MJ, Kim MJ, Jang HS, Kang JS, Kang J

  • KMID: 1709211
  • J Biomed Res.
  • 2014 Jun;15(2):92-95.
Renal dysplasia is a developmental disorder of the renal parenchyma involving anomalous differentiation. It is characterized by persistent metanephric ducts surrounded by primitive mesenchyme, fetal or immature glomeruli, fetal or...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Partial Tetrasomy of Chromosome 22q11.1 Resulting from a Supernumerary Isodicentric Marker Chromosome in a Boy with Cat-eye Syndrome

Ko JM, Kim JB, Pai KS, Yun JN, Park SJ

The 22q11 region has been implicated in chromosomal rearrangements that result in altered gene dosage, leading to three different congenital malformation syndromes: DiGeorge syndrome, cat-eye syndrome (CES), and der(22) syndrome....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
PAX2 Expression in Renal Dysplasia

Lee YH, Jung WH, Hong SW, Jeong HJ

  • KMID: 2073775
  • Korean J Pathol.
  • 2007 Apr;41(2):69-78.
BACKGROUND: Renal dysplasia is the abnormal development of the kidney. The condition is usually detected in childhood along with other urinary tract anomalies, but can remain unnoticed until adulthood. It...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Multicystic Renal Dysplasia with Ipsilateral Ectopic Ureteral Orifice and Seminal Vesicle Cyst: A case report

Son HJ, Kim JH, Kang MJ

  • KMID: 1979396
  • Korean J Pathol.
  • 2000 Apr;34(4):310-313.
Renal dysplasia results from aberrant metanephric histogenesis caused fundamentally by a defect in inducer tissue or responding tissue. Dysplastic kidneys vary tremendously in gross and microscopic appearance but are characterized...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Cushing's syndrome due to Primary Pimary Pigmented Nodular Adrenal Dysplasia ( PPNAD ): A Case of Carney's Complex

Yoo SJ, Cha BY, Lee KW, Son HY, Kang SK, Kim YS, Lee JM, Won JM

  • KMID: 2100251
  • J Korean Soc Endocrinol.
  • 1997 Mar;12(1):90-98.
Primary Pigmented Nodular Adrenal Dysplasia (PPNAD) is a rare cause of Cushing's syndrome in infants and young adults. The familial occurrence, it may be variably associated with a complex of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Congenital Cystic Disease of the Kidney overview and a classification

Joo M, Kim YM, Kim CJ, Suh YL, Seo JW, Chi JG

  • KMID: 1725229
  • Korean J Pathol.
  • 1997 Mar;31(3):233-243.
The congenital renal cystic disease encompasses a complex group of pathologic and clinical entities. We retrospectively reviewed 42 cases of congenital renal cystic lesions classified into four Potter types in...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Renal Dysplasia: A Clinicopathologic Review of Six Cases

Kang GH, Kim JO, Kim BK, Suh KS

  • KMID: 2275774
  • Korean J Pathol.
  • 1997 Jan;31(1):34-39.
Renal dysplasia results from aberrant histogenesis in metanephric differentiation. It is characterized morphologically by abnormal organization and a persistence of primitive structures, such as cartilage, undifferentiated mesenchyme, and immature tubules....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Beckwith-Wiedemann Syndrome with Unusual Sialoadenomegaly

Han HS, Lee SS, Lee SK, Chi JG

  • KMID: 1725166
  • Korean J Pathol.
  • 1996 Oct;30(10):939-942.
Beckwith-Wiedemann syndrome is a rare clinical entity characterized by exomphalos, macroglossia, macrosomia, and renal hyperplasia/dysplasia. Although its entity is established, its etiology and obligatory features have not been settled. We...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Multicystic Renal Dysplasia associated with Ectopic Ureteral Orifice

Kang SM, Park YK, Lee JH, Chai SE, Yang MH

  • KMID: 1724328
  • Korean J Pathol.
  • 1988 Sep;22(3):331-335.
A case of unilateral multicystic renal dysplasia was reported in view of rarity, and a review of literature 23-year-old female was admitted to Kyung Hee University Hospital with a complaint...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Ectopic Ureter Entering Seminal Vesicle Associated with Ectopic Renal Dysplasia

Chang SK, Mah SY

  • KMID: 1912447
  • Korean J Urol.
  • 1987 Aug;28(4):585-587.
We presented one case of 43 years old man with ectopic ureter entering the seminal vesicle associated with ectopic renal dysplasia. He had complained of perineal and lower abdominal discomfort,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Renal Dysplasia with Single Vaginal Ectopic ureter: Report of 1 Case

Park JS, Yoon MS, Chun CS

  • KMID: 2289819
  • Korean J Urol.
  • 1985 Oct;26(5):537-539.
We report one case in which delayed enhanced computerized tomography (1.5 hr. later) contributed in detecting a dysplastic kidney with a single vaginal ectopic ureter that had been nonfunctioning on...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr