Familial disturbance of fibrin monomer aggregation.

Suppr

超能文献

作者信息

Von Felten A, Duckert F, Frick P G

出版信息

Br J Haematol. 1966 Nov;12(6):667-77. doi: 10.1111/j.1365-2141.1966.tb00152.x.

DOI:10.1111/j.1365-2141.1966.tb00152.x

PMID:5927094

Abstract

摘要

相似文献

Familial disturbance of fibrin monomer aggregation.

Br J Haematol. 1966 Nov;12(6):667-77. doi: 10.1111/j.1365-2141.1966.tb00152.x.

Enzymatic method for the quantitative determination of factor. XIII. Application to a familial deficiency.

Pathol Eur. 1970;5(3):315-30.

Dysfibrinogenemia in a patient with primary hepatoma. First observation of an acquired abnormality of fibrin monomer aggregation.

N Engl J Med. 1969 Feb 20;280(8):405-9. doi: 10.1056/NEJM196902202800802.

Congenital deficiency of fibrin-stabilizing factor. Report of a case and family study.

JAMA. 1969 Jan 27;207(4):751-3.

[Familial dysfibrinogenemia with abnormal nonomer aggregation. Paris III fibrinogen].

Pathol Biol (Paris). 1974 Nov;22 suppl:72-9.

Developments in transient hemorrhagic disorders.

Tex Med. 1973 Feb;69(2):72-8.

New families with hereditary hemorrhagic trait due to deficiency of fibrin stabilizing factor (F. 13).

Thromb Diath Haemorrh. 1968 Dec 31;20(3):534-41.

Fibrinogen Amsterdam, another hereditary abnormality of fibrinogen.

Br J Haematol. 1971 Mar;20(3):287-98. doi: 10.1111/j.1365-2141.1971.tb07039.x.

Dysfibrinogenaemia characterized by abnormal fibrin monomer polymerization and normal fibrinopeptide A release.

Br J Haematol. 1980 Mar;44(3):483-94. doi: 10.1111/j.1365-2141.1980.tb05918.x.

[Hereditary dysfibrinogenaemia. Study of a family (author's transl)].

Sem Hop. 1979;55(33-34):1507-12.

引用本文的文献

Fibrinogen Philadelphia. A hereditary hypodysfibrinogenemia characterized by fibrinogen hypercatabolism.

J Clin Invest. 1974 Feb;53(2):600-11. doi: 10.1172/JCI107595.

Chromatographic, ultracentrifugal, and related studies of fibrinogen "Baltimore".

J Clin Invest. 1969 Sep;48(9):1656-62. doi: 10.1172/JCI106130.

Functional evaluation of an inherited abnormal fibrinogen: fibrinogen "Baltimore".

J Clin Invest. 1971 Sep;50(9):1874-84. doi: 10.1172/JCI106680.

Fibrinogen Bethesda: a congenital dysfibrinogenemia with delayed fibrinopeptide release.

J Clin Invest. 1971 Sep;50(9):1819-30. doi: 10.1172/JCI106673.

Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin.

J Clin Invest. 1969 Dec;48(12):2251-9. doi: 10.1172/JCI106191.

Molecular deficiencies of human blood coagulation.

Experientia. 1972 Jan 15;28(1):1-7. doi: 10.1007/BF01928228.

Hereditary disorders of blood coagulation due to defective and deficient synthesis of protein.

Trans Am Clin Climatol Assoc. 1971;82:114-23.

Fibrinogen St. Louis: a new inherited fibrinogen variant, coincidentally associated with hemophilia A.

J Clin Invest. 1972 Mar;51(3):590-7. doi: 10.1172/JCI106848.

A sensitive latex agglutination method for the detection of soluble fibrin in plasma.

Blut. 1977 Dec;35(6):465-79. doi: 10.1007/BF00996693.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验