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

FIBRINOGEN NEW ORLEANS: HEREDITARY DYSFIBRINOGEMIA WITH AN AALPHA CHAIN ABNORMALITYANDES WA; CHAVIN SI; BELTRAN G et al.1982; THROMB. RES.; ISSN 0049-3848; USA; DA. 1982; VOL. 25; NO 1-2; PP. 41-50; BIBL. 24 REF.Article

FIBRINOGEN PETOSKEY: IDENTIFICATION OF A NEW DYSFIBRINOGENEMIA CHARACTERIZED BY ALTERED RELEASE OF FIBRINOPEPTIDE AHIGGINS DL; PENNER JA; SHAFER JA et al.1981; THROMB. RES.; ISSN 0049-3848; USA; DA. 1981; VOL. 23; NO 6; PP. 491-504; BIBL. 40 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 MANCHESTER: IDENTIFICATION OF AN ABNORMAL FIBRINOPEPTIDE A WITH A C-TERMINAL ARGININE->HISTIDINE SUBSTITUTIONSOUTHAN C; KEHL M; HENSCHEN A et al.1983; BRITISH JOURNAL OF HAEMATOLOGY; ISSN 0007-1048; GBR; DA. 1983; VOL. 54; NO 1; PP. 143-151; BIBL. 2 P.Article

AN ABNORMAL INHERITED FIBRINOGEN (FIBRINOGEN GENOVA) WITH DELAYED FIBRIN AGGREGATIONHASSAN HJ; ORLANDO M; TONINI GP et al.1982; SCAND. J. HAEMATOL.; ISSN 0036-553X; DNK; DA. 1982; VOL. 29; NO 4; PP. 287-294; BIBL. 33 REF.Article

PROTHROMBIN GAINESVILLE. A DYSPROTHROMBINEMIA IN A PAIR OF IDENTICAL TWINSSMITH LG; COONE LAH; KITCHENS CS et al.1981; AM. J. HEMATOL.; ISSN 0361-8609; USA; DA. 1981; VOL. 11; NO 3; PP. 223-231; BIBL. 30 REF.Article

FIBRINOGEN MARSEILLE: A NEW CASE OF CONGENITAL DYSFIBRINOGENAEMIASORIA J; SORIA C; JUHAN I et al.1980; HAEMOSTASIS; CHE; DA. 1980; VOL. 9; NO 4; PP. 214-225; BIBL. 18 REF.Article

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FACTOR X FRIULI COAGULATION DISORDER. REPORT OF A NEWLY RECOGNIZED PATIENT AND SOME CONSIDERATIONS ON THE FREQUENCY OF THE DISEASE IN THE FRIULI AREAGIROLAMI A; FALOMO R; DE MARCO L et al.1976; ACTA HAEMATOL.; SUISSE; DA. 1976; VOL. 56; NO 1; PP. 27-38; BIBL. 18 REF.Article

FACTOR VII PADUA 1. ANOTHER CASECROZE M; BRIZARD CP.1982; HAEMOSTASIS; ISSN 0301-0147; CHE; DA. 1982; VOL. 11; NO 3; PP. 185-188; BIBL. 12 REF.Article

AN ABNORMAL FIBRINOGEN WITH DELAYED FIBRINOPEPTIDE A RELEASELANE DA; VANROSS M; KAKKAR VV et al.1980; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1980; VOL. 46; NO 1; PP. 89-98; BIBL. 18 REF.Article

DYSFIBRINOGENEMIE CONGENITALE: DEUX OBSERVATIONSAMSELLEM M; SAMAMA M; CONARD J et al.1978; NOUV. PRESSE MED.; FRA; DA. 1978; VOL. 7; NO 41; PP. 3745-3748; ABS. ENG; BIBL. 14 REF.Article

A FURTHER INHERITED VARIANT OF COAGULATION FACTOR XPARKIN JD; MADARAS F; SWEET B et al.1974; AUSTRAL. NEW ZEAL. J. MED.; AUSTRAL.; DA. 1974; VOL. 4; NO 6; PP. 561-564; BIBL. 15REF.Article

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

FACTOR X FRIULI: AN IMMUNOLOGICAL STUDY IN PLASMA AND IN SERUM USING SEVERAL METHODS = FACTEUR X FRIULI: ETUDE IMMUNOLOGIQUE DANS LE PLASMA ET LE SERUM A L'AIDE DE PLUSIEURS METHODESGIROLAMI A; BAREGGI G; BORSATO N et al.1975; BLUT; DTSCH.; DA. 1975; VOL. 30; NO 3; PP. 203-212; ABS. ALLEM.; BIBL. 1P.Article

LE DISFIBRINOGENEMIE CONGENITE ED ACQUISITE = LES DYSFIBRINOGENEMIES CONGENITALES ET ACQUISESPONARI O; POTI R.1975; HAEMOTOLOGICA; ITAL.; DA. 1975; VOL. 60; NO 1; PP. 96-116; ABS. ANGL.; BIBL. 4P.Article

CROSSOVER ELECTROPHORESIS (ELECTROSYNERESIS) VISUALIZATION OF THE ABNORMAL FACTOR X (FACTOR X FRIULI) = VISUALISATION PAR L'ELECTROPHORESE (ELECTROSYNERESE) DU FACTEUR X ANORMAL (FACTEUR X FRIULI)GIROLAMI A; STICCHI A; BAREGGI G et al.1972; J. LAB. CLIN. MED.; U.S.A.; DA. 1972; VOL. 80; NO 5; PP. 740-747; BIBL. 1P.Serial Issue

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