CONGENITAL DYSPROTHROMBINEMIA - AN INHERITED STRUCTURAL DISORDER OF HUMAN PROTHROMBIN

被引：73

作者：

SHAPIRO, SS

MARTINEZ, J

HOLBURN, RR

机构：

来源：

JOURNAL OF CLINICAL INVESTIGATION | 1969年 / 48卷 / 12期

关键词：

D O I：

10.1172/JCI106191

中图分类号：

R-3 [医学研究方法]; R3 [基础医学];

学科分类号：

1001 ;

摘要：

[No abstract available]

引用

页码：2251 / &

共 56 条

[1]

ALPER CA, 1969, IN PRESS

[2] ANTIBODIES TO PAPAIN . A SELECTIVE FRACTIONATION ACCORDING TO INHIBITORY CAPACITY [J].

ARNON, R ;

SHAPIRA, E .

BIOCHEMISTRY, 1967, 6 (12) :3942-&

[3] CHROMATOGRAPHIC ANALYSIS OF ACTIVATION OF HUMAN PROTHROMBIN WITH HUMAN THROMBOKINASE [J].

ARONSON, DL ;

MENACHE, D .

BIOCHEMISTRY, 1966, 5 (08) :2635-&

[4]

BARNHART MI, 1962, THROMB DIATH HAEMOST, V8, P21

[5]

BECK EA, 1964, BLOOD, V24, P853

[6] X-LINKED RECESSIVE INHERITANCE IN EHLERS-DANLOS SYNDROME [J].

BEIGHTON, P .

BMJ-BRITISH MEDICAL JOURNAL, 1968, 3 (5615) :409-+

[7]

BIGGS R, 1966, TREATMENT HEMOPHILIA, P241

[8]

BIGGS R, 1962, HUMAN BLOOD COAGULAT, P67

[9] FIBRINOGEN DETROIT - A MOLECULAR DEFECT IN N-TERMINAL DISULPHIDE KNOT OF HUMAN FIBRINOGEN [J].

BLOMBACK, M ;

BLOMBACK, B ;

MAMMEN, EF ;

PRASAD, AS .

NATURE, 1968, 218 (5137) :134-&

[10] A STUDY OF A CASE OF CONGENITAL HYPOPROTHROMBINAEMIA [J].

BORCHGREVINK, CF ;

EGEBERG, O ;

POOL, JG ;

SKULASON, T ;

STORMORKEN, H ;

WAALER, B .

BRITISH JOURNAL OF HAEMATOLOGY, 1959, 5 (03) :294-301

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