A NEW CONGENITAL HAEMORRHAGIC CONDITION DUE TO PRESENCE OF AN ABNORMAL FACTOR-X (FACTOR-X-FRIULI) - STUDY OF A LARGE KINDRED

被引:167
作者
GIROLAMI, A
MOLARO, G
LAZZARIN, M
SCARPA, R
BRUNETTI, A
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D O I
10.1111/j.1365-2141.1970.tb01615.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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页码:179 / &
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共 44 条
[1]  
ASCARI R, 1964, MINERVA MED, V326, P2873
[2]  
BACHMANN F, 1957, Schweiz Med Wochenschr, V87, P1221
[3]  
BACHMANN F, 1958, THROMB DIATH HAEMOST, V2, P24
[4]   A NEW INHERITED COAGULATION DISORDER CAUSED BY AN ABNORMAL FIBRINOGEN (FIBRINOGEN BALTIMORE) [J].
BECK, EA ;
CHARACHE, P ;
JACKSON, DP .
NATURE, 1965, 208 (5006) :143-&
[5]  
Biggs R., 1962, HUMAN BLOOD COAGULAT
[6]  
BRECHER C, 1950, J APPLIED PHYSIOL, V3, P365
[7]   IMPROVEMENT OF FACTOR-X DEFICIENCY DURING PREGNANCY [J].
BRODY, JI ;
FINCH, SC .
NEW ENGLAND JOURNAL OF MEDICINE, 1960, 263 (20) :996-999
[8]  
CAEN J, 1958, REV FR ETUD CLIN BIO, V3, P161
[9]  
CARTWRIGHT GE, 1963, DIAGNOSTIC LABORATOR
[10]  
CHEVALLIER P, 1959, Sangre (Barc), V30, P525