A NEW VARIANT OF HUMAN PROTHROMBIN: PROTHROMBIN METZ, DEMONSTRATION IN A FAMILY SHOWING DOUBLE HETEROZYGOSITY FOR CONGENITAL HYPOPROTHROMBINEMIA AND DYSPROTHROMBINEMIAJOSSO F; RIO Y; BEGUIN S et al.1982; HAEMOSTASIS; ISSN 0301-0147; CHE; DA. 1982; VOL. 12; NO 4; PP. 309-316; BIBL. 15 REF.Article

ETUDE FONCTIONNELLE D'UN FIBRINOGENE ANORMAL: LE FIBRINOGENE BONDY = ABNORMAL FIBRINOGEN STUDY: BONDY FIBRINOGENJANDROT PERRUS M.1981; ; FRA; DA. 1981; 109 P.; 30 CM; BIBL. 112 REF.; TH. 3E CYCLE: SCI./PARIS 11/1981/3029Thesis

PROTHROMBIN HOUSTON: A DYSPROTHROMBIN INDENTIFIABLE BY CROSSED IMMUNOELECTROFOCUSING AND ABNORMAL ECHIS CARINATUS VENOM ACTIVATIONWEINGER RS; RUDY C; MOAKE JL et al.1980; BLOOD; ISSN 0006-4971; USA; DA. 1980; VOL. 55; NO 5; PP. 811-816; BIBL. 38 REF.Article

PURIFICATION AND PROPERTIES OF AN ABNORMAL BLOOD COAGULATION FACTOR IX (FACTOR IX_BM)/KINETICS OF ITS INHIBITION OF FACTOR X ACTIVATION BY FACTOR VII AND BOVINE TISSUE FACTOROSTERUD B; KASPER CK; LAVINE KK et al.1981; THROMB. HAEMOST.; ISSN 0340-6245; DEU; DA. 1981; VOL. 45; NO 1; PP. 55-59; BIBL. 21 REF.Article

AN ABNORMAL FIBRINOGEN IN A VENEZUELAN FAMILY.DE BOSCH NB; AROCHA PINANGO CL; SORIA J et al.1977; THROMBOSIS RES.; G.B.; DA. 1977; VOL. 10; NO 2; PP. 253-265; BIBL. 2 P. 1/2Article

FIBRINOGEN CHAPEL HILL II: DEFECTIVE IN REACTIONS WITH THROMBIN FACTOR XIII A AND PLASMINCARRELL N; MCDONAGH J.1982; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1982; VOL. 52; NO 1; PP. 35-47; BIBL. 2 P.Article

FIBRINOGEN HOUSTON: A DYSFIBRINOGEN EXHIBITING DEFECTIVE FIBRIN MONOMER AGGREGATION AND ALPHA -CHAIN CROSS-LINKAGESWEINGER RS; RUDY C; MOAKE JL et al.1980; AM. J. HEMATOL.; ISSN 0361-8609; USA; DA. 1980; VOL. 9; NO 3; PP. 237-248; BIBL. 29 REF.Article

PROTHROMBIN MADRID: A NEW FAMILIAL ABNORMALITY OF PROTHROMBINBEZEAUD A; GUILLIN MC; OLMEDA F et al.1979; THROMBOSIS RES.; GBR; DA. 1979; VOL. 16; NO 1-2; PP. 47-58; BIBL. 35 REF.Article

LES DYSFIBRINOGENEMIES HEREDITAIRES. RAPPORT D'UNE ETUDE FAMILIALEVOINNESSON A; SALAUN M.1979; SEM. HOP.; FRA; DA. 1979; VOL. 55; NO 33-34; PP. 1507-1512; ABS. ENG; BIBL. 6 REF.Article

FURTHER STUDIES ON FACTOR VII PADUA DEFECT: THE REPORT OF THE FOURTH HOMOZYGOUS PATIENT FROM THE SAME VALLEYGIROLAMI A; GAIO A; DOGLIONI L et al.1982; BLUT; ISSN 0006-5242; DEU; DA. 1982; VOL. 44; NO 6; PP. 363-369; BIBL. 14 REF.Article

TWO MORE ABNORMAL FIBRINOGENS (LONDON III AND SYDNEY) WITH IMPAIRED FIBRINOPEPTIDE RELEASELANE DA; IRELAND H; THOMPSON E et al.1982; THROMBOSIS RESEARCH; ISSN 0049-3848; USA; DA. 1982; VOL. 28; NO 6; PP. 821-824; BIBL. 5 REF.Article

CONGENITAL DYSFIBRINOGENEMIAS: MOLECULAR ABNORMALITIES OF FIBRINOGEN.MAMMEN EF.1976; BLUT; DTSCH.; DA. 1976; VOL. 33; NO 4; PP. 229-234; BIBL. 1 P. 1/2Article

COMPARISON OF PROCOAGULANT ACTIVITIES IN EXTRACTS OF NORMAL AND MALIGNANT HUMAN TISSUEGORDON SG; FRANKS JJ; LEWIS BJ et al.1979; J. NATION. CANCER INST.; USA; DA. 1979; VOL. 62; NO 4; PP. 773-776; BIBL. 35 REF.Article

STUDIES OF PLATELET FIBRINOHEN FROM A SUBJECT WITH A CONGENITAL PLASMA FIBRINOGEN ABNORMALITY (FIBRINOGEN PARIS I)JANDROT PERRUS M; MOSESSON MW; DENNINGER MH et al.1979; BLOOD; USA; DA. 1979; VOL. 54; NO 5; PP. 1109-1116; BIBL. 39 REF.Article

DYSFIBRINOGENAEMIE. ZUGLIECH EIN NEUER FALL: DYSFIBRINOGENAEMIE GIESSEN III. = LA DYSFIBRINOGENEMIE. UN CAS NOUVEAU: DYSFIBRINOGENEMIE GIESSEN IIMATTHIAS FR; KRAUSE WH; GANSSERT S et al.1977; KLIN. WSCHR.; DTSCH.; DA. 1977; VOL. 55; NO 11; PP. 539-543; ABS. ANGL.; BIBL. 31 REF.Article

PLASMIC DEGRADATION OF FIBRINOGEN PARIS I.BUDZINSKI AZ; MARDER VJ.1976; J. LAB. CLIN. MED.; U.S.A.; DA. 1976; VOL. 88; NO 5; PP. 817-825; BIBL. 1 P. 1/2Article

COMPARATIVE STUDIES ON THE STRUCTURES OF THE CARBOHYDRATE MOIETIES OF HUMAN FIBRINOGEN AND ABNORMAL FIBRINOGEN NAGOYAMIZUOCHI T; TANIGUCHI T; ASAMI Y et al.1982; J. BIOCHEM. (TOKYO); ISSN 0021-924X; JPN; DA. 1982; VOL. 92; NO 1; PP. 283-293; BIBL. 32 REF.Article

FACTOR VII PADIA: A CONGENITAL COAGULATION DISORDER DUE TO AN ABNORMAL FACTOR VII WITH A PECULIAR ACTIVATION PATTERN.GIROLAMI A; FABRIS F; DAL BO ZANON R et al.1978; J. LAB. CLIN. MED.; U.S.A.; DA. 1978; VOL. 91; NO 3; PP. 387-395; BIBL. 26 REF.Article

PROTHROMBIN MOLISE: A "NEW" CONGENITAL DYSPROTHROMBINEMIA, DOUBLE HETEROZYGOSIS WITH AN ABNORMAL PROTHROMBIN AND "TRUE" PROTHROMBIN DEFICIENCYGIROLAMI A; COCCHERI S; PALARETI G et al.1978; BLOOD; USA; DA. 1978; VOL. 52; NO 1; PP. 115-125; BIBL. 40 REF.Article

SYMPOSIUM ON FIBRINOGEN AND DISFIBRINOGENEMIA.1978; BIBL. HAEMATOL.; CHE; DA. 1978; NO 44; PP. 105-173; BIBL. DISSEM.Article

A KINETIC METHOD FOR CHARACTERIZATION OF HETEREGENOUS FIBRINOGEN AND ITS APPLICATION TO FIBRINOGEN GRAND RAPIDS, A CONGENITAL DYSFIBRINOGENEMIAHIGGINS DL; LEWIS SD; PENNER JA et al.1982; THROMB. HAEMOST.; ISSN 0340-6245; DEU; DA. 1982; VOL. 48; NO 2; PP. 182-186; BIBL. 36 REF.Article

FIBRINOGEN BETHESDA. III. A HYPODYSFIBRINOGENEMIA.GRAINICK HR; COLLER BS; FRATANTONI JC et al.1979; BLOOD; USA; DA. 1979; VOL. 53; NO 1; PP. 28-46; BIBL. 71 REF.Article

FIBRINOGENES QUEBEC I ET QUEBEC II: DEUX NOUVELLES FAMILLES DE DYSFIBRINOGENEMIE.JOBIN F; VU L; DELAGE JM et al.1978; ACTA HAEMATOL.; SUISSE; DA. 1978; VOL. 59; NO 2; PP. 119-127; ABS. ANGL; BIBL. 1 P. 1/2Article

FIBRINOGEN HANNOVER EIN WEITERES ATYPISCHES FIBRINOGEN. = LE FIBRINOGENE HANOVRE, UN AUTRE FIBRINOGENE ATYPIQUEBARTHELS M; SANDVOSS G.1977; BLUT; DTSCH.; DA. 1977; VOL. 34; NO 2; PP. 99-106; ABS. ANGL.; BIBL. 23 REF.Article

APPARENT "DOMINANT" AND "RECESSIVE" INHERITANCE OF VON WILLEBRAND'S DISEASE WITHIN THE SAME KINDREDS. POSSIBLE BIOCHEMICAL MECHANISMSBLOOM AL; PEAKE IR.1979; THROMBOSIS RES.; GBR; DA. 1979; VOL. 15; NO 3-4; PP. 505-512; BIBL. 18 REF.Article