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A Case of dyskeratosis congenita

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  • KMID: 2038927
  • Korean J Dermatol.
  • 1990 Apr;28(2):231-235.
No abstract available.
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A Case of Dyskeratosis Congenita in a Woman

Kim CY, Kim TH, Yoon TJ

  • KMID: 2303157
  • Korean J Dermatol.
  • 2001 Oct;39(10):1162-1165.
No abstract available.
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A case of dyskeratosis congenita

Han JW, Bae JW, Choi WG, Kim HK, Lee KS

  • KMID: 2252496
  • Korean J Hematol.
  • 1991 Oct;26(2):425-428.
No abstract available.
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A Case of Dyskeratosis Congenita

Kim DH, Kang HA, Park HJ, Kim CW, Kim HO

Dyskeratosis congenita is a rare genodermatosis of ectodermal dysplasia, which is characterized by the diagnostic triad consisting of reticulated hyperpigmentation, dystrophic nails, and leukoplakia. There is a predisposition to malignancy,...
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Interstitial Lung Disease in a Patient with Dyskeratosis Congenita

Kim HJ, Kim KJ, Lee KH, Shin KC, Chung JH, Hyun MS, Kim KH

  • KMID: 2320253
  • Tuberc Respir Dis.
  • 2013 Feb;74(2):70-73.
Dyskeratosis congenita is a rare congenital disorder characterized by a triad of reticular pigmentation of the skin, dystrophic nails, and leukoplakia of the mucous membrane. Sometimes it is associated with...
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Dyskeratosis Congenita

Oh S, Kim BD, Lee DH, Lee KH

  • KMID: 1619903
  • Korean J Dermatol.
  • 2003 Mar;41(3):377-380.
Dyskeratosis congenita is a rare multisystemic genodermatosis of ectodermal dysplasia, and is characterized by the diagnostic triad consisting of reticulated hyperpigmentation, dystrophic nails, and leukoplakia. Complications such a malignancy and...
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A Case of Dyskeratosis Congenita

Choi DY, Koh CJ

  • KMID: 2085655
  • Korean J Dermatol.
  • 1988 Oct;26(5):739-743.
Dyskeratosis congsnita is a rare congenital disorder characterized by the triad of reticular pigmentation of the skin. dystrophic naila, and leukoplakia of the mucous membrane, and is often associated with...
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A Case of Dyskeratosis Congenita with Myelodysplastic Syndrome

Shin HJ, Poo CS, Kim JS, Bae WH, Hong JH, Chung JS, Lee EY, Cho GJ

  • KMID: 1533978
  • Korean J Hematol.
  • 1999 Nov;34(4):614-618.
Dyskeratosis congenita is a rare form of ectodermal dysplasia consisting of dystrophic nails, reticular hyperpigmentation and leukoplakia, that is often associated with aplastic anemia. We have experienced a 17 year-old-man...
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A Case of Familial Telangiectasia of Face

Ahn SY, Suh SB

  • KMID: 1664743
  • Korean J Dermatol.
  • 1977 Dec;15(4):459-463.
A case of familial telangiectasia of face resembling lupus erythematosus but no having other involved symptoms, except ichthyosis vulgaris of lower legs in all 4 sisters, appeared on 8 months...
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Dyskeratosis Congenita in a Girl

Yi JS, Kook H, Paik HJ, Kim SY, Choi IS, Kim SJ, Sohn KR, Nam HS, Hwang TJ

  • KMID: 2278307
  • Korean J Pediatr Hematol Oncol.
  • 2003 Oct;10(2):293-298.
Dyskeratosis congenita (DC) is a rare genetic disorder encompassing abnormal skin pigmentation, dystrophic nails, leukoplakia of mucous membranes and others. Bone marrow failure is the cause of early mortality. Moreover,...
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Current insights into inherited bone marrow failure syndromes

Chung NG, Kim M

  • KMID: 2353160
  • Korean J Pediatr.
  • 2014 Aug;57(8):337-344.
Inherited bone marrow failure syndrome (IBMFS) encompasses a heterogeneous and complex group of genetic disorders characterized by physical malformations, insufficient blood cell production, and increased risk of malignancies. They often...
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The Frequency of Glycophosphatidyl Inositol-Anchored Protein-Negative Paroxysmal Nocturnal Hemoglobinuria Cells in Pediatric Aplastic Anemia Analyzed by Flow Cytometry

Kim SJ, Kook H, Cho D, Kim SY, Noh HY, Choi IS, Lee JS, Ryang DW, Hwang TJ

  • KMID: 2278261
  • Korean J Pediatr Hematol Oncol.
  • 2003 Apr;10(1):39-48.
PURPOSE: Paroxysmal nocturnal hemoglobinuria (PNH) has been known to be a late clonal complication of aplastic anemia (AA). Flow cytometric analysis using CD55 and CD59 antibodies became the gold standard...
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