COMBINED CONGENITAL DEFICIENCY OF FACTOR-5 AND FACTOR-8 - REPORT OF A FURTHER CASE WITH SOME CONSIDERATIONS ON HEREDITARY TRANSMISSION OF THIS DISORDER

被引:26
作者
GIROLAMI, A [1 ]
GASTALDI, G [1 ]
PATRASSI, G [1 ]
GALLETTI, A [1 ]
机构
[1] UNIV PADUA,MED SCH,INST SEMEIOTICA MED,VIA OSPEDALE CIVILLE 43,PADUA,ITALY
关键词
D O I
10.1159/000208020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:234 / 243
页数:10
相关论文
共 26 条
[1]  
ARAPAKIS G, 1973, 4TH P C INT SOC THRO, P62
[2]   A METHOD FOR THE STUDY OF ANTIHAEMOPHILIC GLOBULIN INHIBITORS WITH REFERENCE TO 6 CASES [J].
BIGGS, R ;
BIDWELL, E .
BRITISH JOURNAL OF HAEMATOLOGY, 1959, 5 (04) :379-395
[3]  
de Vries S I, 1968, Ned Tijdschr Geneeskd, V112, P741
[4]   FACTOR-VIII IMMUNOLOGICAL ASSAY - EVALUATION OF SEVERAL METHODS USING WHOLE PLASMA [J].
GIROLAMI, A ;
STICCHI, A ;
BARBUI, T ;
BAREGGI, G .
BLUT, 1974, 29 (05) :309-316
[5]   COMBINED HEREDITARY DEFICIENCY OF FACTOR-7 AND FACTOR-8 - DISTINCT COAGULATION DISORDER DUE TO LACK OF AN AUTOSOMAL GENE CONTROLLING FACTOR-7 AND FACTOR-8 ACTIVATION [J].
GIROLAMI, A ;
VENTURELLI, R ;
CELLA, G ;
VIRGOLINI, L ;
BURUL, A .
ACTA HAEMATOLOGICA, 1976, 55 (03) :181-191
[6]   CONGENITAL COMBINED FACTOR-V AND FACTOR-VIII DEFICIENCY IN A MALE BORN FROM A BROTHER-SISTER INCEST [J].
GIROLAMI, A ;
BRUNETTI, A ;
DEMARCO, L .
BLUT, 1974, 28 (01) :33-42
[7]   HEMORRHAGIC VARICELLA IN PARAHEMOPHILIA [J].
GIROLAMI, A ;
SCARPA, R ;
CADROBBI, P .
BLUT, 1972, 25 (05) :293-+
[8]   PARAHEMOPHILIA - CASE REPORT [J].
GIROLAMI, A ;
VENTURELLI, R ;
RIGHINI, F ;
SCARPA, R .
ACTA HAEMATOLOGICA, 1971, 46 (04) :242-+
[9]   REPORT OF A CASE OF CONGENITAL AFIBRINOGENEMIA [J].
GIROLAMI, A ;
VENTURELLI, R ;
BAREGGI, G .
BLUT, 1972, 24 (01) :23-+
[10]  
GIROLAMI A, 1970, Acta Haematologica (Basel), V44, P164