ASSOCIATED VON WILLEBRAND DISEASE AS A POSSIBLE CAUSE OF LACK OF THROMBOSIS IN AN AT-III ABNORMALITY (AT-III TRENTO)

被引:16
作者
GIROLAMI, A [1 ]
CAPPELLATO, MG [1 ]
VICARIOTO, MA [1 ]
CASONATO, S [1 ]
MARAFIOTI, F [1 ]
机构
[1] UNIV PADUA, SCH MED, CHAIR MED 2, I-35100 PADUA, ITALY
来源
BLUT | 1986年 / 52卷 / 01期
关键词
D O I
10.1007/BF00320139
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:29 / 33
页数:5
相关论文
共 26 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]   ABNORMAL MIGRATION OF SERUM ANTITHROMBIN-III IN PATIENTS ON COUMARIN THERAPY BY CROSS-IMMUNOELECTROPHORESIS [J].
ANTONIO, G ;
GIOVANNI, P ;
CRISTINA, V ;
VITTORIO, P .
BRITISH JOURNAL OF HAEMATOLOGY, 1981, 49 (03) :490-492
[3]  
BLOMBACK M, 1974, THROMB RES, V5, P621, DOI 10.1016/0049-3848(74)90052-8
[4]  
CLARKE HGM, 1968, CLIN SCI, V35, P403
[5]   INHERITED ANTITHROMBIN DEFICIENCY CAUSING THROMBOPHILIA [J].
EGEBERG, O .
THROMBOSIS ET DIATHESIS HAEMORRHAGICA, 1965, 13 (3-4) :516-&
[6]  
GIROLAMI A, 1983, Folia Haematologica (Leipzig), V110, P98
[7]  
GIROLAMI A, 1978, J LAB CLIN MED, V91, P387
[8]   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
[9]  
GIROLAMI A, 1978, BLOOD, V52, P115
[10]   COMBINED CONGENITAL DEFICIENCY OF FACTOR-5 AND FACTOR-8 - REPORT OF A FURTHER CASE WITH SOME CONSIDERATIONS ON HEREDITARY TRANSMISSION OF THIS DISORDER [J].
GIROLAMI, A ;
GASTALDI, G ;
PATRASSI, G ;
GALLETTI, A .
ACTA HAEMATOLOGICA, 1976, 55 (04) :234-243