遗传性前转变素（凝血因子VII）缺乏症的临床及家系研究。 - Suppr

A CLINICAL AND FAMILY STUDY OF HEREDITARY PROCONVERTIN (FACTOR VII) DEFICIENCY.

作者信息

HALL C A, RAPAPORT S I, AMES S B, DEGROOT J A

出版信息

Am J Med. 1964 Aug;37:172-81. doi: 10.1016/0002-9343(64)90003-8.

DOI:10.1016/0002-9343(64)90003-8

PMID:14206751

Abstract

摘要

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A CLINICAL AND FAMILY STUDY OF HEREDITARY PROCONVERTIN (FACTOR VII) DEFICIENCY.

Am J Med. 1964 Aug;37:172-81. doi: 10.1016/0002-9343(64)90003-8.

EXCHANGE TRANSFUSION IN HEREDITARY FACTOR VII (PROCONVERTIN) DEFICIENCY.

Am J Clin Pathol. 1965 Aug;44:198-202. doi: 10.1093/ajcp/44.2.198.

CLINICAL ASPECTS OF CONGENITAL FACTOR VII DEFICIENCY.

Am J Med. 1964 Aug;37:182-94. doi: 10.1016/0002-9343(64)90004-x.

[DURATION OF LIFE OF PROCONVERTIN (FACTOR VII)].

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Thrombo-embolism in patients with total proconvertin (factor VII) deficency. A report on two cases.

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[SOME PROBLEMS OF THE ANTICOAGULANT TREATMENT OF DEEP VENOUS THROMBOSIS IN PREGNANCY].

Orv Hetil. 1964 Jun 21;105:1162-5.

CONGENITAL DEFICIENCY OF FACTOR VII (HYPOCONVERTINEMIA). CRITICAL REVIEW OF LITERATURE AND REPORT OF THREE CASES, WITH EXTENSIVE PEDIGREE STUDY AND EFFECT OF TRANSFUSIONS.

Am J Med. 1964 Jul;37:71-91. doi: 10.1016/0002-9343(64)90213-x.

[Gastrectomy in a patient presenting a moderate hypoproconvertinemia].

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[APROPOS OF HYPOPROCONVERTINEMIA].

Klin Med (Mosk). 1963 Aug;41:57-61.

Thromboembolism in congenital factor VII deficiency.

Acta Haematol. 1984;71(1):60-2. doi: 10.1159/000206513.

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[Clinical studies of familial hereditary factor VII deficiency (author's transl)].

Blut. 1981 May;42(5):297-306. doi: 10.1007/BF00996846.

Binding of human factor VII and VIIa to monocytes.

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Haemostatic mechanism in uraemia.

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J Med Genet. 1965 Dec;2(4):254-303. doi: 10.1136/jmg.2.4.254.

Circulating anticoagulant to factor 8 associated with rheumatoid arthritis.

Br Med J. 1969 Dec 20;4(5685):726-7. doi: 10.1136/bmj.4.5685.726.

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A CLINICAL AND FAMILY STUDY OF HEREDITARY PROCONVERTIN (FACTOR VII) DEFICIENCY.

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