HEREDITARY PROTEIN-S DEFICIENCY - CLINICAL MANIFESTATIONS

被引：368

作者：

ENGESSER, L

BROEKMANS, AW

BRIET, E

BROMMER, EJP

BERTINA, RM

机构：

[1] UNIV HOSP LEIDEN, HAEMOSTASIS & THROMBOSIS RES UNIT, BLDG 1-C 2-R, POB 9600, 2300 RC LEIDEN, NETHERLANDS

[2] TNO, GAUBIUS INST, LEIDEN, NETHERLANDS

来源：

ANNALS OF INTERNAL MEDICINE | 1987年 / 106卷 / 05期

关键词：

D O I：

10.7326/0003-4819-106-5-677

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：677 / 682

页数：6

共 34 条

[1] ANTITHROMBIN (HEPARIN COFACTOR) ASSAY WITH NEW CHROMOGENIC SUBSTRATES (S-2238 AND CHROMOZYM-TH) [J].

ABILDGAARD, U ;

LIE, M ;

ODEGARD, OR .

THROMBOSIS RESEARCH, 1977, 11 (04) :549-553

[2]

Abildgaard U., 1981, RECENT ADV BLOOD COA, P151

[3] ABNORMAL PLASMINOGEN - HEREDITARY MOLECULAR ABNORMALITY FOUND IN A PATIENT WITH RECURRENT THROMBOSIS [J].

AOKI, N ;

MOROI, M ;

SAKATA, Y ;

YOSHIDA, N .

JOURNAL OF CLINICAL INVESTIGATION, 1978, 61 (05) :1186-1195

[4]

BERTINA RM, 1985, THROMB HAEMOSTASIS, V53, P268

[5]

BERTINA RM, 1982, THROMB HAEMOSTASIS, V48, P1

[6]

BERTINA RM, 1984, THROMB HAEMOSTASIS, V51, P1

[7]

BITHELL TC, 1985, CLIN CHEM, V31, P509

[8]

BROEKMANS AW, 1985, THROMB HAEMOSTASIS, V53, P273

[9]

BROEKMANS AW, 1985, HAEMOSTASIS, V15, P233

[10]

BROEKMANS AW, 1983, THROMB HAEMOSTASIS, V49, P251

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