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[Dominant mild hemophilia AB with prolonged bleeding time as a subgroup of pseudohemophilias].

作者信息

MARX R, FRUHMANN G

出版信息

Klin Wochenschr. 1958 Dec 1;36(23):1109-18. doi: 10.1007/BF01482177.

DOI:10.1007/BF01482177
PMID:13612117
Abstract
摘要

相似文献

1
[Dominant mild hemophilia AB with prolonged bleeding time as a subgroup of pseudohemophilias].[以出血时间延长为特征的显性轻度血友病AB作为假性血友病的一个亚组]
Klin Wochenschr. 1958 Dec 1;36(23):1109-18. doi: 10.1007/BF01482177.
2
Nasal spray desmopressin (DDAVP) for mild hemophilia A and von Willebrand disease.用于轻度甲型血友病和血管性血友病的鼻腔喷雾去氨加压素(DDAVP)。
Ann Intern Med. 1991 Apr 1;114(7):563-8. doi: 10.7326/0003-4819-114-7-563.
3
Desmopressin: a nontransfusional treatment of hemophilia and von Willebrand disease.去氨加压素:一种血友病和血管性血友病的非输血治疗方法。
Haemostasis. 1992;22(5):276-80. doi: 10.1159/000216335.
4
[GENEALOGIC AND CLINICAL STUDY OF A CASE OF HEMOPHILIA A WITH LENGTHENING OF THE BLEEDING TIME (ANGIOHEMOPHILIA A)].1例出血时间延长的甲型血友病(血管性甲型血友病)的系谱与临床研究
Haematol Lat. 1964 Apr-Jun;7:111-24.
5
DDAVP: a useful alternative to blood components in moderate hemophilia A and von Willebrand disease.去氨加压素:中度甲型血友病和血管性血友病中血液成分的有效替代物。
J Pediatr. 1983 Feb;102(2):228-33. doi: 10.1016/s0022-3476(83)80526-5.
6
Hemophilia and von Willebrand's disease: 2. Management. Association of Hemophilia Clinic Directors of Canada.血友病和血管性血友病:2. 管理。加拿大血友病诊所主任协会
CMAJ. 1995 Jul 15;153(2):147-57.
7
Hemophilia And Von Willebrand Disease In Children: Emergency Department Evaluation And Management.儿童血友病和血管性血友病:急诊科评估与管理
Pediatr Emerg Med Pract. 2015 Sep;12(9):1-20; quiz 20-1.
8
[The factor VIII complex: hemophilia A and von Willebrand disease].[凝血因子VIII复合物:甲型血友病和血管性血友病]
Sem Hop. 1982 Sep 30;58(35):2032-6.
9
Assessment of bleeding for the evaluation of therapeutic preparations in small animal models of antibody-induced hemophilia and von Willebrand disease.在抗体诱导的血友病和血管性血友病疾病的小动物模型中,对治疗制剂评估时的出血情况评估
Thromb Haemost. 1997 Mar;77(3):591-9.
10
Inherited abnormalities of coagulation: hemophilia, von Willebrand disease, and beyond.遗传性凝血异常:血友病、血管性血友病及其他。
Pediatr Clin North Am. 2013 Dec;60(6):1419-41. doi: 10.1016/j.pcl.2013.09.002.

引用本文的文献

1
[ON THE PATHOGENESIS OF THE VON WILLEBRAND-JUERGENS SYNDROME. A CLINICAL AND SUBMICROSCOPICAL STUDY].[关于血管性血友病-于尔根斯综合征的发病机制。一项临床及亚显微镜研究]
Klin Wochenschr. 1964 May 15;42:491-501. doi: 10.1007/BF01484132.

本文引用的文献

1
Combined hemophilia and PTC deficiency.血友病合并凝血酶原复合物缺乏症。
Blood. 1955 Apr;10(4):357-61.
2
A new familial thrombopathy.
Thromb Diath Haemorrh. 1957 Aug 15;1(2):261-3.
3
[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.
4
[Predisposition for bleeding and coagulation disorders in uremia].[尿毒症患者出血与凝血障碍的易感性]
Klin Wochenschr. 1958 Feb 1;36(3):107-12. doi: 10.1007/BF01500451.
5
Studies on antihemophilic globulin.抗血友病球蛋白的研究。
Acta Paediatr Suppl (Upps). 1958 Apr;47(Suppl 114):1-32.
6
Haemophilia and related conditions: a survey of 187 cases.
Br J Haematol. 1958 Jan;4(1):1-27. doi: 10.1111/j.1365-2141.1958.tb03830.x.
7
[New method for comparative quantitative determination of thrombocyte adhesiveness on surfaces other than blood with simultaneous observation on relative viscosity of blood].[一种用于比较定量测定血小板在非血液表面的黏附性并同时观察血液相对黏度的新方法]
Blut. 1957 Sep;3(5):247-54. doi: 10.1007/BF01630770.
8
[Angio-hemophilia A and B: nonhemophilic hemorrhagic diathesis with congenital deficiency of antihemophilic globulin-(factor IX)].血管性血友病A和B:伴有抗血友病球蛋白(因子IX)先天性缺乏的非血友病性出血素质
Folia Haematol (Frankf). 1957 Apr;1(3):251-67.
9
[Direct phase-microscopic counting of thrombocytes and reticulocytes].[血小板和网织红细胞的直接相差显微镜计数]
Arztl Forsch. 1956 Nov 10;10(11):I/552-5.
10
Vascular hemophilia; a familial hemorrhagic disease in males and females characterized by combined antihemophilic globulin deficiency and vascular abnormality.血管性血友病;一种男女均可患的家族性出血性疾病,其特征为抗血友病球蛋白联合缺乏和血管异常。
Pediatrics. 1956 Sep;18(3):347-61.