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名词信息
中 文 名:
先天性转铁蛋白缺乏症
英 文 名:
congenital atransferrinemia
中文又称:
中文曾称:
名词来源:
所属专业:
血液科
所属类别:
疾病诊断名词
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Pubmed相关的文献
congenital atransferrinemia
相关文献:
[Congenital atransferrinemia].
Hromec A, Payer J Jr, Killinger Z, Rybár I, Rovenský J.
Dtsch Med Wochenschr. 1994 May 6;119(18):663-6. doi: 10.1055/s-2008-1058745.
PMID:8187613
Congenital atransferrinemia. A case report and review of the literature.
Hamill RL, Woods JC, Cook BA.
Am J Clin Pathol. 1991 Aug;96(2):215-8. doi: 10.1093/ajcp/96.2.215.
PMID:1862777
A family of congenital atransferrinemia.
Goya N, Miyazaki S, Kodate S, Ushio B.
Blood. 1972 Aug;40(2):239-45.
PMID:4625559
[Congenital atransferrinemia].
Urabe A.
Nihon Rinsho. 1991 Mar;49(3):634-6.
PMID:2041190
A new case of congenital atransferrinemia with a novel splice site mutation: c.293-63del.
Dabboubi R, Amri Y, Yahyaoui S, Mahjoub R, Sahli CA, Sahli C, Hadj Fredj S, Bibi A, Sammoud A, Messaoud T.
Eur J Med Genet. 2020 May;63(5):103874. doi: 10.1016/j.ejmg.2020.103874. Epub 2020 Feb 3.
PMID:32028041
[Congenital atransferrinemia].
HEILMEYER L, KELLER W, VIVELL O, BETKE K, WOEHLER F, KEIDERLING W.
Schweiz Med Wochenschr. 1961 Oct 7;91:1203.
PMID:13906009
[Congenital atransferrinemia. Review of its clinical presentation].
Gaston Morata JL, Rodríguez Cuartero A.
Sangre (Barc). 1982;27(4A):538-41.
PMID:6760430
[Congenital atransferrinemia in a 7-year-old girl].
HEILMEYER L, KELLER W, VIVELL O, KEIDERLING W, BETKE K, WOEHLER F, SCHULTZE HE.
Dtsch Med Wochenschr. 1961 Sep 15;86:1745-51. doi: 10.1055/s-0028-1113001.
PMID:13906010
Molecular analysis of a novel case of congenital atransferrinemia.
Chen C, Wen S, Tan X.
Acta Haematol. 2009;122(1):27-8. doi: 10.1159/000235614. Epub 2009 Aug 20.
PMID:19696475
Severe hypochromic microcytic anemia in a patient with congenital atransferrinemia.
Shamsian BS, Rezaei N, Arzanian MT, Alavi S, Khojasteh O, Eghbali A.
Pediatr Hematol Oncol. 2009 Jul-Aug;26(5):356-62. doi: 10.1080/08880010902973251.
PMID:19579082
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