CONGENITAL AFIBRINOGENEMIA - CASE REPORT WITH SOME CONSIDERATIONS ON HEREDITARY TRANSMISSION OF THIS DISORDER

被引：18

作者：

GIROLAMI, A

ZACCHELLO, G

DELIA, R

机构：

来源：

THROMBOSIS ET DIATHESIS HAEMORRHAGICA | 1971年 / 25卷 / 03期

关键词：

D O I：

10.1055/s-0038-1654320

中图分类号：

R6 [外科学];

学科分类号：

1002 ; 100210 ;

摘要：

引用

页码：460 / +

页数：1

共 38 条

[1]

BACHMANN F, 1958, THROMB DIATH HAEMOST, V2, P24

[2] A NEW INHERITED COAGULATION DISORDER CAUSED BY AN ABNORMAL FIBRINOGEN (FIBRINOGEN BALTIMORE) [J].

BECK, EA ;

CHARACHE, P ;

JACKSON, DP .

NATURE, 1965, 208 (5006) :143-&

[3]

Biggs R., 1962, HUMAN BLOOD COAGULAT

[4]

BOMMER W, 1963, ANN PAEDIATR-BASEL, V200, P180

[5] MORPHOLOGY AND ENUMERATION OF HUMAN BLOOD PLATELETS [J].

BRECHER, G ;

CRONKITE, EP .

JOURNAL OF APPLIED PHYSIOLOGY, 1950, 3 (06) :365-377

[6]

CARTWRIGHT GE, 1963, DIAGNOSTIC LABORATOR

[7]

CAUSSADE L, 1954, PRESSE MED, V62, P1040

[8] FIBRINOLYTIC AND PROTEOLYTIC ACTIVITY OF A HUMAN PLASMINOGEN, PREPARED FROM FRACTION-III OF HUMAN PLASMA [J].

CLIFFTON, EE ;

CANNAMELA, D .

JOURNAL OF APPLIED PHYSIOLOGY, 1953, 6 (01) :42-50

[9] SPECIFIC ASSAY OF PROWER-STUART FACTOR AND FACTOR VII [J].

DENSON, KW .

ACTA HAEMATOLOGICA, 1961, 25 (02) :105-&

[10] CONGENITAL DEFICIENCY OF FIBRINOGEN IN 2 SISTERS - A CLINICAL AND HAEMATOLOGICAL STUDY [J].

DUBE, B ;

AGARWAL, SP ;

GUPTA, MM ;

CHAWLA, SC .

ACTA HAEMATOLOGICA, 1970, 43 (02) :120-&

← 1 2 3 4 →