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超能文献

Dyskeratosis congenita (Zinsser-Engman-Cole syndrome).

作者信息

Ganguly S

机构信息

Department of Pediatrics, IPGME & R and SSKM Hospital, Calcutta.

出版信息

Indian J Pediatr. 1996 Nov-Dec;63(6):823-6. doi: 10.1007/BF02730938.

DOI:10.1007/BF02730938

PMID:10830069

Abstract

摘要

相似文献

Dyskeratosis congenita (Zinsser-Engman-Cole syndrome).

Indian J Pediatr. 1996 Nov-Dec;63(6):823-6. doi: 10.1007/BF02730938.

[Dyskeratosis congenita (Zinsser-Cole-Engman syndrome)].

Ryoikibetsu Shokogun Shirizu. 2000(30 Pt 5):73-5.

[Dyskeratosis congenita in a 40-year-old patient].

Hautarzt. 2006 Apr;57(4):313-5. doi: 10.1007/s00105-005-0937-2.

[Skin lesions, atresia of lacrimal ducts and pancytopenia in a young man. Congenital dyskeratosis or Zinsser-Engman-Cole syndrome].

Rev Clin Esp. 2001 Sep;201(9):545-7. doi: 10.1016/s0014-2565(01)70907-1.

Marathon of eponyms: 26 Zinsser-Engman-Cole syndrome (Dyskeratosis congenita).

Oral Dis. 2012 Jul;18(5):522-3. doi: 10.1111/j.1601-0825.2009.01558.x.

Dyskeratosis congenita: presentation of cutaneous triad in a sporadic case.

BMJ Case Rep. 2018 Nov 28;11(1):e226736. doi: 10.1136/bcr-2018-226736.

[Dyskeratosis congenita, a disease caused by defective telomere maintenance].

Med Sci (Paris). 2008 Apr;24(4):390-8. doi: 10.1051/medsci/2008244390.

Retinal hemorrhages in a patient with dyskeratosis congenita.

J AAPOS. 2008 Aug;12(4):415-7. doi: 10.1016/j.jaapos.2008.01.016. Epub 2008 May 2.

[Gastric adenocarcinoma in Zinsser-Cole-Engman syndrome].

Cir Esp. 2006 Sep;80(3):176-7. doi: 10.1016/s0009-739x(06)70949-6.

Dyskeratosis Congenita: a historical perspective.

Mech Ageing Dev. 2008 Jan-Feb;129(1-2):48-59. doi: 10.1016/j.mad.2007.10.006. Epub 2007 Oct 30.

本文引用的文献

DYSKERATOSIS CONGENITA AND FAMILIAL PANCYTOPENIA.

JAMA. 1965 Apr 19;192:203-8. doi: 10.1001/jama.1965.03080160023005.

Dyskeratosis congenita with pigmentation, dystrophia unguium, and leukoplakia oris; a follow-up report of two brothers.

AMA Arch Derm. 1958 Jun;77(6):704-12. doi: 10.1001/archderm.1958.01560060070012.

Dyskeratosis congenita.

AMA Arch Derm. 1956 Feb;73(2):123-32. doi: 10.1001/archderm.1956.01550020023004.

Evaluation of granulocyte-macrophage colony-stimulating factor for treatment of pancytopenia in children with fanconi anemia.

J Pediatr. 1994 Jan;124(1):144-50. doi: 10.1016/s0022-3476(94)70271-3.

Dyskeratosis congenita: an autosomal dominant disorder.

J Am Acad Dermatol. 1982 Jun;6(6):1034-9. doi: 10.1016/s0190-9622(82)80100-x.

Nail dystrophy in dyskeratosis congenita and chronic graft-vs-host disease.

Arch Dermatol. 1986 May;122(5):506-7.

X-linked dyskeratosis congenita with pancytopenia.

Arch Dermatol. 1978 Nov;114(11):1667-71.

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相似文献

Dyskeratosis congenita (Zinsser-Engman-Cole syndrome).

Indian J Pediatr. 1996 Nov-Dec;63(6):823-6. doi: 10.1007/BF02730938.

[Dyskeratosis congenita (Zinsser-Cole-Engman syndrome)].

Ryoikibetsu Shokogun Shirizu. 2000(30 Pt 5):73-5.

[Dyskeratosis congenita in a 40-year-old patient].

Hautarzt. 2006 Apr;57(4):313-5. doi: 10.1007/s00105-005-0937-2.

[Skin lesions, atresia of lacrimal ducts and pancytopenia in a young man. Congenital dyskeratosis or Zinsser-Engman-Cole syndrome].

Rev Clin Esp. 2001 Sep;201(9):545-7. doi: 10.1016/s0014-2565(01)70907-1.

Marathon of eponyms: 26 Zinsser-Engman-Cole syndrome (Dyskeratosis congenita).

Oral Dis. 2012 Jul;18(5):522-3. doi: 10.1111/j.1601-0825.2009.01558.x.

Dyskeratosis congenita: presentation of cutaneous triad in a sporadic case.

BMJ Case Rep. 2018 Nov 28;11(1):e226736. doi: 10.1136/bcr-2018-226736.

[Dyskeratosis congenita, a disease caused by defective telomere maintenance].

Med Sci (Paris). 2008 Apr;24(4):390-8. doi: 10.1051/medsci/2008244390.

Retinal hemorrhages in a patient with dyskeratosis congenita.

J AAPOS. 2008 Aug;12(4):415-7. doi: 10.1016/j.jaapos.2008.01.016. Epub 2008 May 2.

[Gastric adenocarcinoma in Zinsser-Cole-Engman syndrome].

Cir Esp. 2006 Sep;80(3):176-7. doi: 10.1016/s0009-739x(06)70949-6.

Dyskeratosis Congenita: a historical perspective.

Mech Ageing Dev. 2008 Jan-Feb;129(1-2):48-59. doi: 10.1016/j.mad.2007.10.006. Epub 2007 Oct 30.

本文引用的文献

DYSKERATOSIS CONGENITA AND FAMILIAL PANCYTOPENIA.

JAMA. 1965 Apr 19;192:203-8. doi: 10.1001/jama.1965.03080160023005.

Dyskeratosis congenita with pigmentation, dystrophia unguium, and leukoplakia oris; a follow-up report of two brothers.

AMA Arch Derm. 1958 Jun;77(6):704-12. doi: 10.1001/archderm.1958.01560060070012.

Dyskeratosis congenita.

AMA Arch Derm. 1956 Feb;73(2):123-32. doi: 10.1001/archderm.1956.01550020023004.

Evaluation of granulocyte-macrophage colony-stimulating factor for treatment of pancytopenia in children with fanconi anemia.

J Pediatr. 1994 Jan;124(1):144-50. doi: 10.1016/s0022-3476(94)70271-3.

Dyskeratosis congenita: an autosomal dominant disorder.

J Am Acad Dermatol. 1982 Jun;6(6):1034-9. doi: 10.1016/s0190-9622(82)80100-x.

Nail dystrophy in dyskeratosis congenita and chronic graft-vs-host disease.

Arch Dermatol. 1986 May;122(5):506-7.

X-linked dyskeratosis congenita with pancytopenia.

Arch Dermatol. 1978 Nov;114(11):1667-71.