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May-Hegglin anomaly developing myelodysplasia and acute myeloid leukemia.

作者信息

Fujishima Naohito, Hirokawa Makoto, Ishikawa Hiroyasu, Fujishima Masumi, Kume Masaaki, Miura Ikuo, Sawada Ken-ichi

出版信息

Int J Hematol. 2004 Jun;79(5):505-6. doi: 10.1532/ijh97.03177.

DOI:10.1532/ijh97.03177
PMID:15239405
Abstract
摘要

相似文献

1
May-Hegglin anomaly developing myelodysplasia and acute myeloid leukemia.伴有骨髓发育异常和急性髓系白血病的May-Hegglin异常。
Int J Hematol. 2004 Jun;79(5):505-6. doi: 10.1532/ijh97.03177.
2
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Aleukemic leukemia cutis preceding overt acute myeloid leukemia in myelodysplastic syndrome.骨髓增生异常综合征中，在明显的急性髓系白血病之前出现的无白血病性白血病皮肤浸润。
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Bone marrow morphology and disease progression in congenital thrombocytopenia: a detailed clinicopathologic and genetic study of eight cases.先天性血小板减少症的骨髓形态学与疾病进展：8例详细的临床病理及遗传学研究
Mod Pathol. 2017 Apr;30(4):486-498. doi: 10.1038/modpathol.2016.218. Epub 2017 Jan 6.

本文引用的文献

1
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness.MYH9相关疾病：May-Hegglin异常、Sebastian综合征、Fechtner综合征和Epstein综合征并非独立的疾病实体，而是单一疾病的不同表现形式。
Medicine (Baltimore). 2003 May;82(3):203-15. doi: 10.1097/01.md.0000076006.64510.5c.
2
Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations.MYH9相关疾病中性粒细胞非肌肉肌球蛋白重链A的免疫荧光分析：亚细胞定位与MYH9突变的关联
Lab Invest. 2003 Jan;83(1):115-22. doi: 10.1097/01.lab.0000050960.48774.17.
3
[Vitamin K2 therapy for myelodysplastic syndrome].
[维生素K2治疗骨髓增生异常综合征]
Rinsho Ketsueki. 2002 Feb;43(2):117-21.
4
Menatetrenone, a vitamin K2 analog, ameliorates cytopenia in patients with refractory anemia of myelodysplastic syndrome.甲萘醌四烯，一种维生素K2类似物，可改善骨髓增生异常综合征难治性贫血患者的血细胞减少症。
Ann Hematol. 2002 Jan;81(1):16-9. doi: 10.1007/s00277-001-0391-x. Epub 2001 Dec 8.
5
Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.May-Hegglin异常中编码非肌肉肌球蛋白重链A的MYH9突变。
Nat Genet. 2000 Sep;26(1):106-8. doi: 10.1038/79069.
6
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.MYH9基因的突变会导致May-Hegglin异常以及Fechtner和Sebastian综合征。May-Heggllin/Fechtner综合征研究联盟。
Nat Genet. 2000 Sep;26(1):103-5. doi: 10.1038/79063.
7
What is the difference between May-Hegglin anomaly and Sebastian platelet syndrome?May-Hegglin异常与塞巴斯蒂安血小板综合征之间有何区别？
Int J Hematol. 2000 Jun;71(4):400-1.
8
International scoring system for evaluating prognosis in myelodysplastic syndromes.评估骨髓增生异常综合征预后的国际评分系统。
Blood. 1997 Mar 15;89(6):2079-88.
9
Cellular myosin heavy chain in human leukocytes: isolation of 5' cDNA clones, characterization of the protein, chromosomal localization, and upregulation during myeloid differentiation.
Blood. 1991 Oct 1;78(7):1826-33.