Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

32 results
Display

Pancreaticoblastoma (infantile pancreatic carcinoma): a case report

Park KS, Park YT, Lee DH, Lim JH, Lee SW, Ahn HJ, Shin DH, Choi IJ

Pancreaticoblastoma is a rare nonfunctioning primary malignant neoplasm of the pancrease occuring inchildhood. It arises in the ventral pancreas and is thought to be caused by a disturbance in organogenesis...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Caudal Regression Syndrome Diagnosed by Prenatal Ultrasonography

Moon Y, Kim JH, Ahn OJ, Jeon SW, Hwang BC

  • KMID: 2272638
  • Korean J Obstet Gynecol.
  • 2005 Jul;48(7):1788-1792.
Caudal regression syndrome is rare malformative syndrome characterized by lower vertebral agenesis, accompanied by abnormalities of the pelvis, lower extremities and urogenital malformation. Although the cause is not clear, hyperglycemia...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Recovery, growth and development of Macroorchis spinulosus in albino rats

Woo HC, Chai JY, Hong SJ

The developmental features, growth and organogenesis of Macroorchis spinulosus were observed in albino rats. Globular and thick walled metacercariae, possessed a stylet, Y-shaped excretory bladder and extracecal testes. In albino...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of VATER syndrome

Ha SJ, Chung KH, Lee OK, Kim WS, Lee KH

  • KMID: 1690514
  • J Korean Pediatr Soc.
  • 1993 Apr;36(4):583-588.
The VATER syndrome is a group of congenital anomalies with a nonrandom tendency for concurrence. Defects include vertebral, anorectal malformation, tracheoesophageal fisutla with esophageal atresia, radial-limb, vascular, and renal abnormalities....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Branchio-Otic Syndrome

Kim TY, Eom JW, Kwak HH, Heo KW

Branchio-oto-renal (BOR) syndrome is a clinically heterogeneous autosomal dominant form of syndromic hearing loss characterized by variable hearing impairment, malformations of the pinnae, the presence of branchial arch remnants, and...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Functional Classification of the Congenital Anomalies of the Extremities and Spine

Suk SI, Chung MS, Lee SH, Lee CK, Yoon BH, Lee YI

Various classifications of congenital anomalies of the extremities and spine have been proposed and are in use. Some are based on anatomy, some on embryology, presumed etiology, or therapeutical approach....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Cervical Bronchogenic Cyst Mimicking Thyroid Cyst

Kang SH, Jin SM, Kim HK, Yoon TM

Bronchogenic cysts are rare congenital malformations that result from an abnormal development of the ventral foregut budding of the tracheobronchial tree at the time of organogenesis. They are usually located...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Pregnant Woman with Type 2 Diabetes Unintentionally Exposed to Metformin and Voglibose until the Second Trimester of Pregnancy: A Case Report

Kim YU, Kwak JH, Yeo SH, Moon SS, Lee YS

Use of oral hypoglycemic agents during pregnant women with type 2 diabetes is controversial due to safety issues. Recently, randomized controlled trials support short-term safety of glyburide and metformin for...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Prenatal ultrasonographic diagnosis of Fetus in Fetu at 2nd trimester: A case report

Shim IS, Lee SA, Park MH, Park EA, Kim YJ, Choe GJ, Ahn JJ, Kim JI, Chun SH

  • KMID: 2273121
  • Korean J Obstet Gynecol.
  • 2007 Apr;50(4):673-677.
Fetus in fetu is an very rare condition in which a vertebrate fetus is incorporated within its twin. Although a number of cases were reported at 3rd trimester of gestation...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Is the Gestational Week of Spontaneous Abortion Repeated in the Following Pregnancies in the Recurrent Abortion?

Kang IS, Song JH, Yoo KJ, Noh GW, Baik EC, Jun JY

  • KMID: 2261107
  • Korean J Obstet Gynecol.
  • 1998 Aug;41(8):2094-2096.
During the second or third trimester of pregnancy, a consensus exists that intrauterine fetal death may develop repeatedly around the gestational period of previous fetal death. The purpose of the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Role of the CXC12-CXCR4 Axis and CXCL16 in Inflammatory Bowel Disease

Nakase H, Matsuura M, Mikami S, Uza N, Chiba T

Numerous studies of colitis in IBD (inflammatory bowel diseases) patients and in animal models have demonstrated that both inflammatory cytokines and chemokines are up-regulated in settings of active inflammation. Blockade...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract

Lee KH, Gee HY, Shin JI

The definition of congenital anomalies of the kidney and urinary tract (CAKUT) is the disease of structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux (VUR). These anomalies...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
DNAse I hypersensitive sites of lung specific transcription factor gene

Lee YC

BACKGROUND: Thyroid Transcription Factor-1(TTF-1) acts as a tissue specific transcription factor in the regulation of lung specific gene expression and as morphogenic protein during lung organogenesis. Currently, there is very...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Fetus in Fetu

Kim JY, Yang SH, Hong SY, Choo DH, Oh HK, Park YC, Chung HL, Kim WT

  • KMID: 2280573
  • Korean J Perinatol.
  • 2006 Jun;17(2):225-230.
Fetus in fetu is an extremely uncommon cause of abdominal mass in the neonate with an incidence of 1 in 500,000 births. This is thought to occur when a monozygotic,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Intraductal Papillary Mucinous Neoplasm in a Patient with an Incomplete Pancreatic Divisum

Nam SM, Chung WC, Chin HM, Lee KM, Lee BI, Chang UI, Yang JM, Choi KY, Chung IS

  • KMID: 2415622
  • Korean J Gastrointest Endosc.
  • 2006 Sep;33(3):191-196.
Intraductal papillary mucinous neoplasms (IPMNs) are premalignant lesions that require a surgical resection. IPMN can cause abdominal pain or pancreatitis as a result of either mucin production or a papillary...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Regenerative Medicine of the Bile Duct: Beyond the Myth

Buisson EM, Jeong J, Kim HJ, Choi D

Cholangiopathies are rare diseases of the bile duct with high mortality rates. The current treatment for cholangiopathies is liver transplantation, but there are significant obstacles including a shortage of donors...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of unrecognized pregnancy during chemotherapy in non-small cell lung cancer patient

Park JY, Park JW, Lee DO, Park CW, Park JS, Jun JK, Syn HC

Most chemotherapeutic drugs are known to possess significant teratogenic effects. Although several agents have been proven to be safe for the fetus after organogenesis period, there is limited information on...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Comparison of teratogenecity induced by nano- and micro-sized particles of zinc oxide in cultured mouse embryos

Jung AY, Jung KY, Lin C, Yon JM, Lee JG, Lee BJ, Yun YW, Nam SY

The increasing uses of zinc oxide nanoparticles (nZnO) in industrial and personal care products raise possible danger of using nZnO in human. To determine whether ZnO induces size-dependent anomalies during...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Immunohistochemical identification and quantitative analysis of cytoplasmic Cu/Zn superoxide dismutase in mouse organogenesis

Yon JM, Baek IJ, Lee SR, Kim MR, Lee BJ, Yun YW, Nam SY

Cytoplasmic Cu/Zn superoxide dismutase (SOD1) is an antioxidant enzyme that converts superoxide to hydrogen peroxide in cells. Its spatial distribution matches that of superoxide production, allowing it to protect cells...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Preconception infection and genetic counseling

Ryu KY, Hoh JK, Park MI

Congenital malformations are a common cause of illness, handicapping conditions, and death. Errors of morphogenesis leading to congenital anomalies have many recognized causes, including specific single-gene mutations, chromosome imbalances, and...
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