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Congenital vascular defect associated with platelet abnormality and antihemophilic factor deficiency.

作者信息

RACCUGLIA G, NEEL J V

出版信息

Blood. 1960 Jun;15:807-29.

PMID:14435675
Abstract
摘要

相似文献

1
Congenital vascular defect associated with platelet abnormality and antihemophilic factor deficiency.
Blood. 1960 Jun;15:807-29.
2
Antihaemophilic factor deficiency, capillary defect of von Willebrand type, and idiopathic thrombocytopenia occurring in one family.一个家族中出现的抗血友病因子缺乏症、血管性血友病类型的毛细血管缺陷以及特发性血小板减少症。
J Clin Pathol. 1961 Sep;14(5):540-2. doi: 10.1136/jcp.14.5.540.
3
Occurrence of two hemorrhagic disorders with antihemophilic factor (AHF) deficiency in the same family: classical hemophilia and von willebrand's disease.
J Lab Clin Med. 1963 Mar;61:424-36.
4
Familial association of thrombopathia and antihemophilic factor (AHF, factor VIII) deficiency.血小板病与抗血友病因子(AHF,凝血因子VIII)缺乏的家族性关联。
Blood. 1972 Aug;40(2):227-33.
5
A syndrome of platelet-release abnormality and mild hemophilia.一种血小板释放异常和轻度血友病综合征。
Blood. 1974 Jun;43(6):821-30.
6
[PLATELET ADHESIVITY AND VISCOUS METAMORPHOSIS. STUDY IN VARIOUS HEMORRHAGIC DISEASES].[血小板黏附性与黏性变态。在各种出血性疾病中的研究]
Rev Hosp Clin Fac Med Sao Paulo. 1963 Sep-Oct;18:397-406.
7
Association of the hemophilia A carrier state and hemorrhagic thrombocytopathy with dilatation of the platelet membrane complex.甲型血友病携带者状态及出血性血小板病与血小板膜复合物扩张的关联。
Acta Haematol. 1984;71(6):381-7. doi: 10.1159/000206623.
8
[Classical hemophilia and anti-hemophilic globulin deficiency in heterozygotic women].
Pol Tyg Lek. 1960 Feb 15;15:250-5.
9
An inherited hemorrhagic trait with characteristics resembling both mild hemophilia of type A and Von Willebrand's disease.一种遗传性出血性性状,其特征类似于A型轻度血友病和血管性血友病。
Scand J Clin Lab Invest. 1965;17:Suppl 84:25-32.
10
Vascular hemophilia: the association of a vascular defect with a deficiency of antihemophilic globulin.
Am J Med Sci. 1956 Oct;232(4):421-33.

引用本文的文献

1
Antihaemophilic factor deficiency, capillary defect of von Willebrand type, and idiopathic thrombocytopenia occurring in one family.一个家族中出现的抗血友病因子缺乏症、血管性血友病类型的毛细血管缺陷以及特发性血小板减少症。
J Clin Pathol. 1961 Sep;14(5):540-2. doi: 10.1136/jcp.14.5.540.
2
Genetics of human blood coagulation.人类血液凝固的遗传学
J Med Genet. 1965 Dec;2(4):254-303. doi: 10.1136/jmg.2.4.254.
3
Von Wllebrands disease. Distinction from other syndromes associated with a long bleeding time, and from hemophilia.血管性血友病。与其他出血时间延长相关综合征及血友病的鉴别。
Calif Med. 1969 Aug;111(2):113-9.
4
Detection of heterozygotes in both parents of homozygous patients with Von Willebrand's disease.检测血管性血友病纯合子患者双亲中的杂合子。
J Clin Pathol. 1975 Apr;28(4):309-16. doi: 10.1136/jcp.28.4.309.