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A hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency.

作者信息

DUCKERT F, JUNG E, SHMERLING D H

出版信息

Thromb Diath Haemorrh. 1960 Dec 15;5:179-86.

PMID:13724728
Abstract
摘要

相似文献

1
A hitherto undescribed congenital haemorrhagic diathesis probably due to fibrin stabilizing factor deficiency.一种迄今未被描述的先天性出血素质,可能是由于纤维蛋白稳定因子缺乏所致。
Thromb Diath Haemorrh. 1960 Dec 15;5:179-86.
2
[Hemorrhagic diathesis caused by a deficiency of the fibrin-stabilizing factor (factor 13)].[纤维蛋白稳定因子(因子13)缺乏引起的出血素质]
Verh Dtsch Ges Inn Med. 1968;74:144-7.
3
[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.
4
[Isolated congenital factor V deficiency as cause of hemorrhagic diathesis].
Wien Z Inn Med. 1959 Jan;40(1):10-6.
5
[Studies on fibrinolysis in hemorrhagic diathesis].
Arztl Forsch. 1958 Mar 10;12(3):I/157-60.
6
A form of haemorrhagic diathesis characterized by the lack of the third clotting-factor, normally present in blood-platelets (thrombopathia haemophilica).
Ann Paediatr. 1953 Oct;181(4):193-200.
7
[Complex hemorrhagic diathesis with fibrinolysis in cancer of prostate].
Lyon Med. 1955 Apr 24;87(17):397-403.
8
Two cases of haemorrhagic disease arising from fibrin stabilizing factor deficiency.
Hemostase. 1966;6(5):317-24.
9
[Hemorrhagic diathesis due to factor VII deficiency (hypoproconvertinemia)].
Ned Tijdschr Geneeskd. 1954 Oct 16;98(42):2987-3001.
10
Haemorrhagic diathesis due to a deficiency of factor VII (hypoproconvertinaemia).由于凝血因子 VII 缺乏(低凝血酶原血症)导致的出血素质。
Acta Haematol. 1955 Jul;14(1):43-56. doi: 10.1159/000204970.

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Subgaleal Hematoma in a Female With Normal Coagulation Tests.凝血功能检查正常女性的帽状腱膜下血肿
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Clinical Profile of Congenital Factor XIII Deficiency in Children.儿童先天性凝血因子 XIII 缺乏症的临床特征。
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Identification of a novel mutation in the factor XIII A subunit in a patient with inherited factor XIII deficiency.鉴定一名遗传性因子 XIII 缺乏症患者的因子 XIII A 亚基中的新型突变。
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Genetic Spectrum in F13A1 Detected by Next-Generation Sequencing Among North Indian Patients with FXIII Deficiency.下一代测序检测北印度FXIII缺乏症患者中F13A1的基因谱
Indian J Hematol Blood Transfus. 2023 Apr;39(2):276-283. doi: 10.1007/s12288-022-01579-1. Epub 2022 Nov 1.
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Peptidic Inhibitors and a Fluorescent Probe for the Selective Inhibition and Labelling of Factor XIIIa Transglutaminase.多肽抑制剂和荧光探针用于选择性抑制和标记因子 XIIIa 转谷氨酰胺酶。
Molecules. 2023 Feb 8;28(4):1634. doi: 10.3390/molecules28041634.
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The potential impact of coagulation factor XIII in trauma-induced coagulopathy - a retrospective case series analysis.凝血因子 XIII 在创伤性凝血病中的潜在影响-回顾性病例系列分析。
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Case Report: Use of endobronchial Watanabe spigot and coagulation factor XIII supplementation in the treatment of persistent pneumothorax due to pneumocystis pneumonia with human immunodeficiency virus infection.病例报告:使用支气管内渡边栓子及补充凝血因子 XIII 治疗人类免疫缺陷病毒感染合并肺孢子菌肺炎所致的持续性气胸。
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Characterization of laboratory coagulation parameters and risk factors for intraventricular hemorrhage in extremely premature neonates.极早产儿凝血实验室参数特征及颅内出血的危险因素。
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Postpartum Hemorrhage in Heterozygote Factor XIII Deficient Women Compared With Healthy Women. A Cross-Sectional Experience From Iran.伊朗的一项横断面研究:杂合子 FXIII 缺乏症妇女与健康妇女产后出血的比较。
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Mild Acquired Factor XIII Deficiency and Clinical Relevance at the ICU-A Retrospective Analysis.轻度获得性因子 XIII 缺乏症与 ICU 临床相关性:一项回顾性分析。
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