FACTOR-VII PADUA2 - ANOTHER FACTOR-VII ABNORMALITY WITH DEFECTIVE OX BRAIN THROMBOPLASTIN ACTIVATION AND A COMPLEX HEREDITARY PATTERN

被引:0
作者
GIROLAMI, A
CATTAROZZI, G
DALBOZANON, R
CELLA, G
TOFFANIN, F
机构
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:46 / 53
页数:8
相关论文
共 22 条
  • [1] ALEXANDER B, 1951, J CLIN INVEST, V30, P237
  • [2] A NEW INHERITED COAGULATION DISORDER CAUSED BY AN ABNORMAL FIBRINOGEN (FIBRINOGEN BALTIMORE)
    BECK, EA
    CHARACHE, P
    JACKSON, DP
    [J]. NATURE, 1965, 208 (5006) : 143 - &
  • [3] VARIANT OF FACTOR-IX DEFICIENCY IN FEMALE WITH 45, X TURNERS SYNDROME
    BITHELL, TC
    PIZARRO, A
    MACDIARMID, WD
    [J]. BLOOD-THE JOURNAL OF HEMATOLOGY, 1970, 36 (02): : 169 - +
  • [4] MOLECULAR VARIANT OF FACTOR-VII
    BRIET, E
    LOELIGER, EA
    VANTILBURG, NH
    VELTKAMP, JJ
    [J]. THROMBOSIS AND HAEMOSTASIS, 1976, 35 (02) : 289 - 294
  • [5] DENSON KWE, 1972, LANCET, V1, P1234
  • [6] AN INVESTIGATION OF 3 PATIENTS WITH CHRISTMAS DISEASE DUE TO AN ABNORMAL TYPE OF FACTOR 9
    DENSON, KWE
    BIGGS, R
    MANNUCCI, PM
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 1968, 21 (02) : 160 - &
  • [7] GIROLAMI A, 1977, BLOOD, V50, P603
  • [8] GIROLAMI A, 1978, J LAB CLIN MED, V91, P387
  • [9] 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
    GIROLAMI, A
    VENTURELLI, R
    CELLA, G
    VIRGOLINI, L
    BURUL, A
    [J]. ACTA HAEMATOLOGICA, 1976, 55 (03) : 181 - 191
  • [10] GIROLAMI A, 1974, J LAB CLIN MED, V84, P654