奥兰群岛（维勒布兰德-于尔根斯）血栓形成病中的抗血友病球蛋白（因子VIII）缺乏症 - Suppr

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超能文献

[Antihemophilic globulin (factor VIII) deficiency in Aland (Willebrand-Jürgens) thrombopathy].

作者信息

JURGENS R, LEHMANN W, WEGELIUS O, ERIKSSON A W, HIEPLER E

出版信息

Thromb Diath Haemorrh. 1957 Aug 15;1(2):257-60.

PMID:13580992

Abstract

摘要

相似文献

[Antihemophilic globulin (factor VIII) deficiency in Aland (Willebrand-Jürgens) thrombopathy].奥兰群岛（维勒布兰德-于尔根斯）血栓形成病中的抗血友病球蛋白（因子VIII）缺乏症

Thromb Diath Haemorrh. 1957 Aug 15;1(2):257-60.

[Associated prolonged bleeding time & anti-hemophilic globulin deficiency in a female; a variant of the von Willebrand-Jürgens thrombopathy].[一名女性患者出现相关的出血时间延长及抗血友病球蛋白缺乏；血管性血友病-于尔根斯血栓病的一种变异型]

Ned Tijdschr Geneeskd. 1958 Jul 26;102(30):1454-9.

[On Willebrand-Jürgens constitutional thrombopathy in the Aland Islands].关于奥兰群岛的维勒布兰德-于尔根斯体质性血栓形成病

Schweiz Med Wochenschr. 1951 Dec 15;81(50):1248-53.

[New studies on thrombopathy (v. Willebrand-Jurgens) at Aland Islands, Finland].[芬兰奥兰群岛血栓形成病（血管性血友病-尤尔根斯病）的新研究]

Acta Genet Med Gemellol (Roma). 1959;8:38-42.

[Notes on a case of the Willebrand-Jurgens type of thrombopathy].[一例维勒布兰德 - 尤尔根斯型血栓形成异常的病例记录]

Pediatria (Napoli). 1958 Jan-Feb;66(1):83-97.

[Thrombopathy Willebrand-Jurgens or angiohemophilia].[血管性血友病（维勒布兰德-于尔根斯病）或血管性血友病]

Medizinische. 1958 Apr 12;12(15):601-5.

[Problem of Willebrand-Jurgens thrombopathy of pseudohemophilia respectively female hemophilia; epicrisis of an almost 20 year study].[分别关于假性血友病（血管性血友病 - 于尔根斯病）或女性血友病的问题；近20年研究的补记]

Z Kinderheilkd. 1957;79(4):449-64.

[Ultrastructure of thrombocytes in constitutional Willebrand-Jürgens thrombopathy with an observation on submicroscopic orthology of thrombocytes].[先天性血管性血友病（维勒布兰德-于尔根斯病）中血小板的超微结构及血小板亚微观同源性观察]

Thromb Diath Haemorrh. 1958 Sep 1;2(3-4):300-23.

[Pseudo-hemophilic constitutional thrombopathy of Willebrand-Jurgens with presence of an anticoagulant substance and osteoarthropathy].[伴有抗凝物质及骨关节病的维勒布兰德-于尔根斯假性血友病体质性血栓病]

Praxis. 1958 Jun 5;47(23):558-61.

[Associated congenital deficiency of antihemophilic globulin (factory VIII) and proaccelerin (factor V) in two siblings. Clinical, biologic and genetic study].[两名同胞中抗血友病球蛋白（因子VIII）和加速素（因子V）相关先天性缺乏。临床、生物学和遗传学研究]

Minerva Med. 1965 Dec 19;56(101):4464-70.

引用本文的文献

Von Willebrand's Disease: Pathogenesis and Management.血管性血友病：发病机制与管理

J R Coll Physicians Lond. 1969 Apr;3(3):211-222.

Historical perspective and future directions in platelet research.血小板研究的历史视角与未来方向。

J Thromb Haemost. 2011 Jul;9 Suppl 1(Suppl 1):374-95. doi: 10.1111/j.1538-7836.2011.04356.x.

[Blood platelets and coagulationactive plasma proteins. A short summary of their function and pathology].[血小板与具有凝血活性的血浆蛋白。其功能与病理学简述]

Blut. 1962 May;8:171-82. doi: 10.1007/BF01631173.

[Research on thrombopathy (von Willebrand-Juergen)].

Klin Wochenschr. 1961 Jan 1;39:32-42. doi: 10.1007/BF01498796.

Bibliography of human genetics.人类遗传学文献目录。

Am J Hum Genet. 1959 Jun;11(2 Part 1):208-14 contd.

[Thrombocyte factor III activity decrease in thrombopathy].

Klin Wochenschr. 1959 Mar 1;37(5):227-30. doi: 10.1007/BF01491925.

[A sensitive method for determination of thrombocytin factor-3 activity in the thromboplastin generation test].[凝血活酶生成试验中血小板第3因子活性测定的一种灵敏方法]

Klin Wochenschr. 1958 Jun 15;36(12):585-6. doi: 10.1007/BF01497875.

Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland Islands.奥兰群岛血管性血友病家族中血管性血友病因子基因的突变

Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):7937-40. doi: 10.1073/pnas.90.17.7937.

The history of haemophilia.血友病的历史。

J Clin Pathol. 1976 Jun;29(6):469-79. doi: 10.1136/jcp.29.6.469.

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