NO EXCESS MORTALITY IN HETEROZYGOTES FOR HEREDITARY PROTEIN-C DEFICIENCY TYPE-I - 1820 TO 1993

被引:0
作者
ALLAART, CF [1 ]
ROSENDAAL, FR [1 ]
NOTEBOOM, WMP [1 ]
BRIET, E [1 ]
机构
[1] LEIDEN UNIV HOSP,HAEMOSTASIS & THROMBOSIS RES CTR,2333 AA LEIDEN,NETHERLANDS
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:1252 / 1252
页数:1
相关论文
共 50 条
  • [31] HEREDITARY PROTEIN-C DEFICIENCY DUE TO A FRAMESHIFT MUTATION IN EXON-IX OF THE PROTEIN-C GENE
    YAMAMOTO, K
    TANIMOTO, M
    MATSUSHITA, T
    SUGIURA, I
    TAKAMATSU, J
    SAITO, H
    THROMBOSIS AND HAEMOSTASIS, 1991, 65 (06) : 646 - 646
  • [32] THE GENETIC ABNORMALITIES IN A PANEL OF 40 DUTCH FAMILIES WITH SYMPTOMATIC PROTEIN-C DEFICIENCY TYPE-I - HETEROGENEITY AND FOUNDER EFFECTS
    REITSMA, PH
    POORT, BR
    VANDERVELDEN, PA
    ALLAART, RF
    BRIET, E
    BERTINA, RM
    THROMBOSIS AND HAEMOSTASIS, 1991, 65 (06) : 647 - 647
  • [33] HEREDITARY PROTEIN-C DEFICIENCY AND PORTAL-VEIN THROMBOSIS
    DOSSANTOS, JN
    SILVA, AME
    ALEXANDRINO, P
    SALDANHA, T
    CARRAGETA, MO
    FERREIRA, E
    DEPADUA, F
    NETHERLANDS JOURNAL OF MEDICINE, 1991, 38 (5-6) : 212 - 216
  • [34] THE FREQUENCY OF TYPE-I HETEROZYGOUS PROTEIN-S AND PROTEIN-C DEFICIENCY IN 141 UNRELATED YOUNG-PATIENTS WITH VENOUS THROMBOSIS
    GLADSON, CL
    SCHARRER, I
    HACH, V
    BECK, KH
    GRIFFIN, JH
    THROMBOSIS AND HAEMOSTASIS, 1988, 59 (01) : 18 - 22
  • [35] Type-I protein-C deficiency caused by disruption of a hepatocyte nuclear factor (HNF)-6/HNF-1 binding site in the human protein-C gene promoter
    Spek, A
    Reitsma, P
    TRENDS IN CARDIOVASCULAR MEDICINE, 1999, 9 (3-4) : 82 - 85
  • [36] 6 MISSENSE MUTATIONS ASSOCIATED WITH TYPE-I AND TYPE-II PROTEIN-C DEFICIENCY AND IMPLICATIONS OBTAINED FROM MOLECULAR MODELING
    ZHENG, YZ
    SAKATA, T
    MATSUSUE, T
    UMEYAMA, H
    KATO, H
    MIYATA, T
    BLOOD COAGULATION & FIBRINOLYSIS, 1994, 5 (05) : 687 - 696
  • [37] ORAL LOADING OF HOMOGENTISIC ACID IN CONTROLS AND IN OBLIGATE HETEROZYGOTES FOR HEREDITARY TYROSINEMIA TYPE-I
    LABERGE, C
    LESCAULT, A
    GRENIER, A
    MORRISETTE, J
    GAGNE, R
    GADBOIS, P
    HALKET, J
    AMERICAN JOURNAL OF HUMAN GENETICS, 1990, 47 (02) : 329 - 337
  • [38] 2 MUTATIONS IN THE PROMOTER REGION OF THE HUMAN PROTEIN-C GENE BOTH CAUSE TYPE-I PROTEIN-C DEFICIENCY BY DISRUPTION OF 2 HNF-3 BINDING-SITES
    SPEK, CA
    GREENGARD, JS
    GRIFFIN, JH
    BERTINA, RM
    REITSMA, PH
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (41) : 24216 - 24221
  • [39] IMPAIRED SECRETION OF THE ELONGATED MUTANT OF PROTEIN-C (PROTEIN C-NAGOYA) - MOLECULAR AND CELLULAR BASIS FOR HEREDITARY PROTEIN-C DEFICIENCY
    YAMAMOTO, K
    TANIMOTO, M
    EMI, N
    MATSUSHITA, T
    TAKAMATSU, J
    SAITO, H
    JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) : 2439 - 2446
  • [40] HEREDITARY THROMBOPHILIA AS A MULTIGENIC DISEASE - INCREASED THROMBOTIC RISK DUE TO COMBINED HEREDITARY HETEROZYGOUS PROTEIN-C DEFICIENCY AND ACTIVATED PROTEIN-C RESISTANCE
    BRENNER, B
    ZIVELIN, A
    LANIR, N
    GREENGARD, JS
    GRIFFIN, JH
    SELIGSOHN, U
    THROMBOSIS AND HAEMOSTASIS, 1995, 73 (06) : 942 - 942