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Moyamoya Syndrome in a 42-Year-Old Man With Down Syndrome

Ham JH, Song YK, Kim JI, Choi JK, Lee JY

  • KMID: 1966533
  • J Korean Neurol Assoc.
  • 2012 Aug;30(3):230-231.
No abstract available.
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Does wastewater discharge have relations with increase of Turner syndrome and Down syndrome?

Choi I

The purpose of this study is to examine whether water and air pollutants have a relationship with an increase in the genetic disorders Turner syndrome and Down syndrome, which are...
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Three Cases of Primary Hypothyroidism with Down Syndrome in Adult

Lee KW, Shin YG, Lee SK, Lee SK, Chung YS, Kim HM

  • KMID: 2331120
  • J Korean Soc Endocrinol.
  • 1998 Sep;13(3):453-458.
Down syndrome is perhaps the most common genetic condition associated with mental retardation. In cytogenetic examination, trisomy 21 is in 95% of Down syndrome, and the others are mosaicism, translocation...
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A case of monozygotic twin with Down syndrome

Jeon SH, Yoon CH, Kim YW, Kim KB

  • KMID: 2104059
  • J Korean Pediatr Soc.
  • 1993 Mar;36(3):434-438.
No abstract available.
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The incidence of hypothyroidism in children with Down syndrome

Jeon SH, Cho CH, Kim KS, Kim KB

  • KMID: 1691312
  • J Korean Pediatr Soc.
  • 1992 Apr;35(4):534-538.
No abstract available.
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Down Syndrome with Familial Eruptive Syringoma

Chang SH, Yoon TY

  • KMID: 1681247
  • Korean J Dermatol.
  • 1994 Jun;32(3):532-536.
Down syndrome is the most, well known autosomal trisomy and e large number of abnormal skin features have been reported to occur in patients with Down syndromir. including syringoma. Syringomas...
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A case of transient myeloproliferative disorder in Down's syndrome

Kim DU, Lee WK, Park EW, Kim KW

  • KMID: 1691578
  • J Korean Pediatr Soc.
  • 1991 Dec;34(12):1740-1744.
No abstract available.
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A Case of Down-Turner Syndrome

Jeong HJ, Lee ES, Choi KH, Park YH

  • KMID: 2321988
  • J Korean Soc Pediatr Endocrinol.
  • 2005 Jun;10(1):120-124.
Down-Turner syndrome is a rare disease with the incidence of 1 in 2 million. Although Down syndrome with various Turner's karyotype were reported occasionally since a report in 1962, it...
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A Case of Psoriasis in a Patient with Down Syndrome

Kim SY, Yun SJ, Lee JB, Lee SC, Won YH, Kim SJ

  • KMID: 1734200
  • Korean J Dermatol.
  • 2014 Nov;52(11):828-829.
No abstract available.
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Genetic Syndromes associated with Congenital Heart Disease

Ko JM

Recent research has demonstrated that genetic alterations or variations contribute considerably to the development of congenital heart disease. Many kinds of genetic tests are commercially available, and more are currently...
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A case of acute megakaryoblastic leukemia with Down syndrome

Chang SJ, Sohn SM, Kim HS, Kang CM, Jeon DS

  • KMID: 1691576
  • J Korean Pediatr Soc.
  • 1991 Dec;34(12):1730-1735.
No abstract available.
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Posterior nutcracker phenomenon with Down syndrome

Koh ES, Kim MY, Chang YS, Chung S

No abstract available.
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Update on Mental Retardation

Yim SY

  • KMID: 1810940
  • J Korean Acad Rehabil Med.
  • 2006 Apr;30(2):103-110.
Mental retardation is a disability characterized by significant limitations both in intellectual functioning and in adaptive behavior as expressed in conceptual, social, and adaptive skills, which originates before the age...
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A Case of Congenital Cataract in Down's Syndrome

Shin DS, Ahn SK, Koo BS

  • KMID: 2022594
  • J Korean Ophthalmol Soc.
  • 1996 Apr;37(4):708-712.
In most cases of chromosomal anomaly of congenital cataract, the cause is known as Down's syndrome. We experienced a case of bilateral congenital cataract in Trisomy 21 (Down's syndrome). A...
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Papular Elastorrhexis in Down's Syndrome

Shim HC, Jeong YI, Kim G, Song KY, Lee JE, Jue MS, Kim EJ, Park HJ, Joh OJ

  • KMID: 2246604
  • Korean J Dermatol.
  • 2013 Sep;51(9):750-752.
No abstract available.
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A Case of Klinefelter Syndrome Combined with Hydrops Fetalis

Cho JH, Cho EM, Lee CN, Kim BS, Kay CW, Chang SW

  • KMID: 2075256
  • Korean J Obstet Gynecol.
  • 1997 Jul;40(7):1523-1527.
Nonimmune hydrops fetalis(NIHF) is a heterogenous disorder resulting from a vast number of underlying pathologies. Chromsomal abnormalities underlie a large percentage of cases of NIHF in most series. There are...
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Asymptomatic moyamoya syndrome, atlantoaxial subluxation and basal ganglia calcification in a child with Down syndrome

Lee KY, Lee KS, Weon YC

Down syndrome, the most common chromosomal abnormality, may be associated with various neurologic complications such as moyamoya syndrome, cervical spinal cord compression due to atlantoaxial subluxation, and basal ganglia damage,...
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Moyamoya Syndrome: A Window of Moyamoya Disease

Phi JH, Wang KC, Lee JY, Kim SK

Moyamoya-like vasculopathy develops in association with various systemic diseases and conditions, which is termed moyamoya syndrome. Relatively common diseases and conditions are related to moyamoya syndrome, including neurofibromatosis type 1,...
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Clinical considerations of acute leukemia or transient myeloprolifo- rative disorder in Down syndrome

Dong ES, Jang SH, Koo HH, Jung HL, Shin HY, Ahn HS

  • KMID: 1691987
  • J Korean Pediatr Soc.
  • 1991 Jan;34(1):74-82.
No abstract available.
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A study on the atlantoaxial instability in children with Down syndrome

Kim SY, Kim CY

  • KMID: 2335044
  • J Korean Pediatr Soc.
  • 1993 Feb;36(2):179-184.
To evaluate the atlantoaxial instability in children with Down syndrome, the authors analyzed the 97 children with Down syndrome attending to 2 schools for handicaped children in Pusan. The rsults...
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