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COUMARIN-INDUCED ABNORMAL FACTOR IX: AN IMMUNOLOGICAL STUDY IN HUMANSGIROLAMI A; STICCHI A; BURUL A et al.1978; FOLIA HAEMATOL.; DDR; DA. 1978; VOL. 105; NO 1; PP. 117-124; ABS. GER/FRE/RUS; BIBL. 27 REF.Article

CONGENITAL DEFICIENCY OF FACTOR XIII WITH NORMAL SUBUNITS S AND LACK OF SUBUNIT A.GIROLAMI A; BURUL A; STICCHI A et al.1977; ACTA HAEMATOL.; SUISSE; DA. 1977; VOL. 58; NO 1; PP. 17-26; BIBL. 23 REF.Article

DECREASE OF NORMOTEST/THROMBOTEST DISCREPANCY IN NON-CONTACTED COUMARIN PLASMA AFTER GLASS OR ELLAGIC ACID ACTIVATION.GIROLAMI A; PATRASSI G; BURUL A et al.1976; BLUT; DTSCH.; DA. 1976; VOL. 33; NO 1; PP. 41-48; ABS. ALLEM.; BIBL. 1 P. 1/2Article

FURTHER STUDIES ON FACTOR IX ANTIGEN IN HEMOPHILIA BGIROLAMI A; BURUL A; CAPPELLATO G et al.1978; BLUT; DEU; DA. 1978; VOL. 37; NO 4; PP. 215-217; BIBL. 12 REF.Article

COMBINED HEREDITARY DEFICIENCY OF FACTORS VII AND VIII. A DISTINCT COAGULATION DISORDER DUE TO 'LACK' OF AN AUTOSOMAL GENE CONTROLLING FACTOR VII AND VIII ACTIVATIONGIROLAMI A; VENTURELLI R; CELLA G et al.1976; ACTA HAEMATOL.; SUISSE; DA. 1976; VOL. 55; NO 3; PP. 181-191; BIBL. 1 P. 1/2Article

AN IMMUNOLOGICAL INVESTIGATION OF HEMOPHILIA B WITH A TENTATIVE CLASSIFICATION OF THE DISEASE INTO FIVE VARIANTS.GIROLAMI A; STICCHI A; BURUL A et al.1977; VOX SANG.; SUISSE; DA. 1977; VOL. 32; NO 4; PP. 230-238; BIBL. 23 REF.Article

STUDIES ON FACTOR XIII ANTIGEN IN CONGENITAL FACTOR XIII DEFICIENCY. A TENTATIVE CLASSIFICATION OF THE DISEASE IN TWO GROUPS.GIROLAMI A; BURUL A; FABRIS F et al.1978; FOLIA HAEMATOL.; DDR; DA. 1978; VOL. 105; NO 1; PP. 131-141; ABS. GER/FRE/RUS; BIBL. 21 REF.Article

A TENTATIVE CLASSIFICATION OF FACTOR XIII DEFICIENCY IN TWO GROUPS.GIROLAMI A; BURUL A; FABRIS F et al.1977; ACTA HAEMATOL.; SUISSE; DA. 1977; VOL. 58; NO 5; PP. 318-320; BIBL. 5 REF.Article

FAILURE OF TRANEXAMIC ACID TO INFLUENCE THE ELLAGIC ACID-INDUCED HYPERCOAGULABLE STATE.GIROLAMI A; CELLA G; BURUL A et al.1976; FOLIA HAEMATOL.; ALLEM.; DA. 1976; VOL. 103; NO 2; PP. 261-270; ABS. ALLEM. FR. RUSSE; BIBL. 26 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

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