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TABLE RONDE SUR LA MALADIE DE WILLEBRAND1975; ACTUAL. HEMATOL.; FR.; DA. 1975; VOL. 9; PP. 75-108; BIBL. DISSEM.Article

ON VON WILLEBRAND'S DISEASE (VWD)FIRKIN BG; HOWARD MA.1976; BRIT. J. HAEMATOL.; G.B.; DA. 1976; VOL. 32; NO 2; PP. 151-158; BIBL. 2 P.Article

THE SPECTRUM OF VON WILLEBRANDS' DISEASE REVISITED = LQA REVISION DU TABLEAU CLASSIQUE DE LA MALADIE DE VON WILLEBRANDBOWIE EJW; FASS DN; OLSON JD et al.1976; MAYO CLIN. PROC.; U.S.A.; DA. 1976; VOL. 51; NO 1-2; PP. 35-41; BIBL. 46 REF.Article

DETECTION OF HETEROZYGOTES IN BOTH PARENTS OF HOMOZYGOUS PATIENTS WITH VON WILLEBRAND'S DISEASE = DETECTION DES HETEROZYGOTES CHEZ LES 2PARENTS DE SUJETS HOMOZYGOTES ATTEINTS DE MALADIE DE WILLEBRANDSULTAN Y; SIMEON J; CAEN JP et al.1975; J. CLIN. PATHOL.; G.B.; DA. 1975; VOL. 28; NO 4; PP. 309-316; BIBL. 18REF.Article

LE SYNDROME DE VON WILLEBRANDSCHNEIDER P; BACHMANN F; NEEMEH JA et al.1981; MED. HYG.; ISSN 0025-6749; CHE; DA. 1981; VOL. 39; NO 1449; PP. 4353-4361; 5 P.; BIBL. 52 REF.Article

CONCEPTO ACTUAL DE LA ENFERMEDAD DE VON WILLEBRAND = MALADIE DE WILLEBRANDLOPEZ BORRASCA A; VICENTE V; ALBERCA I et al.1978; SANGRE; ESP; DA. 1978; VOL. 23; NO 5B; PP. 708-727; ABS. ENG; BIBL. 58 REF.Article

MESSUNG DER PLAETTCHENADHAESIVITAET MIT EINER MODIFIZIERTEN FORM DER HELLEM II-METHODIK UNTER BESONDER BERUECKSICHTIGUNG DES VON WILLEBRAND-JUERGENS-SYNDROMS = MESURE DE L'ADHESIVITE DES PLAQUETTES AVEC UNE FORME MODIFIEE DE LA METHODE II DE HELLEM, AVEC CONSIDERATION PARTICULIERE DU SYNDROME DE WILLEBRAND-JUERGENSNIESSNER H.1972; THROMBOSIS DIATTESIS HAEMORRHAG.; ALLEM.; DA. 1972; VOL. 27; NO 3; PP. 434-451; ABS. ANGL. FR.; BIBL. 2P.Serial Issue

ELECTROPHORETIC HETEROGENEITY OF NORMAL FACTOR. VIII. VON WILLEBRAND PROTEIN, AND ABNORMAL ELECTROPHORETIC MOBILITY IN PATIENTS WITH VON WILLEBRAND'S DISEASE.SULTAN Y; SIMEON J; CAEN JP et al.1976; J. LAB. CLIN. MED.; U.S.A.; DA. 1976; VOL. 87; NO 2; PP. 185-197; BIBL. 17 REF.Article

ACQUIRED VON WILLEBRAND'S SYNDROMEHOLLAND L; ADAMSON A; INGRAM GIC et al.1980; BRIT. J. HAEMATOL.; GBR; DA. 1980; VOL. 45; NO 1; PP. 161-164; BIBL. 9 REF.Article

MECHANISMS OF PLATELET FUNCTION AS REVEALED BY THE RETENTION OF PLATELETS IN GLASS BEAD COLUMNS = MECANISMES DE LA FONCTION PLAQUETTAIRE REVELES PAR LA RETENTION DES PLAQUETTES DANS DES TUBES DE VERREZUCKER MB; RIFKIN PL; FRIEDBERG NM et al.1972; ANN. NEW YORK ACAD. SCI.; U.S.A.; DA. 1972; VOL. 201; PP. 138-144; BIBL. 32REF.Serial Issue

FAMILIAL ASSOCIATION OF THROMBOPATHIA AND ANTIHEMOPHILIC FACTOR (AHF, FACTOR VIII) DEFICIENCY = ASSOCIATION FAMILIALE D'UNE THROMBOPATHIE ET D'UN DEFICIT EN FACTEUR ANTIHEMOPHILIQUE (AHF, FACTEUR VIII)CROWELL EB JR; EISNER EV.1972; BLOOD; U.S.A.; DA. 1972; VOL. 40; NO 2; PP. 227-233; BIBL. 14 REF.Serial Issue

TYPE IIB VON WILLEBRAND'S DISEASE: DIFFERENTIAL CLEARANCE OF ENDOGENOUS VERSUS TRANSFUSED LARGE MULTIMER VON WILLEBRAND FACTORRUGGERI ZM; LOMBARDI R; GATTI L et al.1982; BLOOD; ISSN 0006-4971; USA; DA. 1982; VOL. 60; NO 6; PP. 1453-1456; BIBL. 7 REF.Article

ADDITIONAL FACTOR XII (HAGEMAN FACTOR) DEFICIENCY IN HEMOPHILIA A AND IN VON WILLEBRAND SYNDROMEBARTHELS M; EDEL J; LIESE B et al.1982; KLIN. WOCHENSCHR.; ISSN 0023-2173; DEU; DA. 1982; VOL. 60; NO 6; PP. 303-309; ABS. ENG; BIBL. 22 REF.Article

STUDIES ON THE PATHOPHYSIOLOGY AND TREATMENT OF VON WILLEBRAND'S DISEASE. IV: MECHANISM OF INCREASED SISTOCETIN-INDUCED PLATELET AGGREGATION IN VON WILLEBRAND'S DISEASETAKAHASHI H.1980; THROMB. RES.; ISSN 0049-3848; USA; DA. 1980; VOL. 19; NO 6; PP. 857-867; BIBL. 40 REF.Article

VON WILLEBRAND'S DISEASE TODAYNILSSON IM; HOLMBERG L.1979; CLIN. IN HAEMATOL.; GBR; DA. 1979; VOL. 8; NO 1; PP. 147-168; BIBL. 5 P.Article

MORBUS VON WILLEBRAND = MALADIE DE WILLEBRANDJACKY E; BLAETTLER W; MUELLER M et al.1979; REV. THERAPEUT.; CHE; DA. 1979; VOL. 36; NO 4; PP. 341-344; ABS. FRE/ENG; BIBL. 18 REF.Article

VON WILLEBRAND'S DISEASE - A COMMON BLEEDING DISORDER.LIAN ECY.1977; ADV. INTERN. MED.; U.S.A.; DA. 1977; VOL. 22; PP. 207-228; BIBL. 4 P.Article

FACTOR-VIII-RELATED ANTIGEN: MEASUREMENT BY ENZYME IMMUNOASSAY = ANTIGENE LIE AU FACTEUR VIII: MESURE PAR DOSAGE IMMUNOLOGIQUE ENZYMATIQUEBARTLETT A; DORMANDY KM; HAWKEY CM et al.1976; BRIT. MED. J.; G.B.; DA. 1976; NO 6016; PP. 994-996; BIBL. 7 REF.Article

IMMUNOLOGIC STUDIES IN VON WILLEBRAND'S DISEASE. ALTERACTION OF FACTOR VII/VON WILLEBRAND PROTEIN AFTER TRANSFUSION WITH PLASMA CONCENTRATES IN PATIENTS WITH VON WILLEBRAND'S DISEASESULTAN Y; SIMEON J; MAISONNEUVE P et al.1976; THROMBOSIS AND HAEMOSTASIS; GERM.; DA. 1976; VOL. 35; NO 1; PP. 110-119; ABS. FR. ALLEM.; BIBL. 1 P.; (CONGR. INT. THROMB. HAEMOSTASIS. 5; PARIS; 1975)Conference Paper

DETERMINATION OF THE VON WILLEBRAND'S DISEASE ANTIGEN (FACTOR VIII-RELATED ANTIGEN) IN PLASMA BY QUANTITATIVE IMMUNOELECTROPHORESIS = MESURE DE L'ANTIGENE DE LA MALADIE DE WILLEBRAND (ANTIGENE DU FACTEUR VIII) DANS LE PLASMA PAR IMMUNOELECTROPHORESE QUANTITATIVEZIMMERMAN TS; HOYER LW; DICKSON L et al.1975; J. LAB. CLIN. MED.; U.S.A.; DA. 1975; VOL. 86; NO 1; PP. 152-159; BIBL. 9 REF.Article

RISTOCIN IN THE DIAGNOSIS OF VON WILLEBRAND'S DISEASE. A COMPARISON OF RATE AND PERCENT OF AGGREGATION WITH LEVELS OF THE PLASMA FACTOR(S) NECESSARY FOR RISTOCETIN AGGREGATION. = LA RISTOCETINE DANS LE DIAGNOSTIC DE LA MALADIE DE VON WILLEBRAND: COMPARAISON DE LA VITESSE ET DU POURCENTAGE D'AGREGATION AVEC LES TAUX DU OU DES FACTEUR(S) PLASMATIQUE(S) NECESSAIRES A L'AGREGATION PAR LA RISTOCETINEDOWLING SV; MUNTZ RH; D'SOUZA S et al.1975; THROMBOSIS DIATHESIS HAEMORRHAG.; ALLEM.; DA. 1975; VOL. 34; NO 2; PP. 465-474; ABS. FR. ALLEM.; BIBL. 22 REF.Article

PLATELET-TYPE VON WILLEBRAND'S DISEASE: CHARACTERIZATION OF A NEW BLEEDING DISORDERMILLER JL; CASTELLA A.1982; BLOOD; ISSN 0006-4971; USA; DA. 1982; VOL. 60; NO 3; PP. 790-794; BIBL. 16 REF.Article

STUDIES OF THE BLOOD PLASMINOGEN ACTIVATOR INDUCED BY 1-DESAMINO-8-D-ARGININE VASOPRESSIN WITH OBSERVATIONS IN VON WILLEBRAND'S DISEASEHOLMBERG L; NILSSON IM; WALLEN P et al.1982; PROC. SOC. EXP. BIOL. MED.; ISSN 0037-9727; USA; DA. 1982; VOL. 170; NO 2; PP. 126-132; BIBL. 27 REF.Article

LE COMPLEXE FACTEUR VIII: L'HEMOPHILIE A ET LA MALADIE DE WILLEBRANDTOBELEM G; ROTHSCHILD C.1982; SEM. HOP.; ISSN 0037-1777; FRA; DA. 1982; VOL. 58; NO 35; PP. 2032-2036; ABS. ENG; BIBL. 6 REF.Article

ACQUIRED VON WILLEBRAND'S DISEASE IN ASSOCIATION WITH WILM'S TUMOR: REGRESSION FOLLOWING TREATMENTSCOTT JP; MONTGOMERY RR; TUBERGEN DG et al.1981; BLOOD; ISSN 0006-4971; USA; DA. 1981; VOL. 58; NO 4; PP. 665-669; BIBL. 27 REF.Article

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