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kw.\*:("WILLEBRAND MALADIE")

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

THE VON WILLEBRAND SYNDROMEBLOOM AL.1980; SEMIN. HEMATOL.; ISSN 0037-1963; USA; DA. 1980; VOL. 17; NO 4; PP. 215-227; BIBL. 83 REF.Article

PLATELET-BOUND RISTOCETIN AGGREGATION FACTOR IN NORMAL SUBJECTS AND PATIENTS WITH VON WILLEBRAND'S DISEASEGREEN D; POTTER EV.1976; J. LAB. CLIN. MED.; U.S.A.; DA. 1976; VOL. 87; NO 6; PP. 976-986; BIBL. 26 REF.Article

VON WILLEBRAND DISEASE AS AN ENDOTHELIAL-CELL ABNORMALITY = LA MALADIE DE WILLEBRAND CONSIDEREE COMME UNE ANOMALIE DES CELLULES ENDOTHELIALESCAEN JP; SULTAN Y.1975; LANCET; G.B.; DA. 1975; NO 7945; PP. 1129; BIBL. 17 REF.Article

VON WILLEBRAND'S DISEASE = LA MALADIE DE VON WILLEBRANDHOLMBERG L; NILSSON IM.1975; ANNU. REV. MED.; U.S.A.; DA. 1975; VOL. 26; PP. 33-44; BIBL. 3P.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

MALADIE DE WILLEBRANDDAUTZENBERG MD; GAZENGEL C.1982; MED. INFANT.; ISSN 0025-6773; FRA; DA. 1982; VOL. 89; NO 2; PP. 211-218; 6 P.; BIBL. 5 REF.Article

AUTOPSY FINDINGS IN AN ELDERLY MAN SUFFERING FROM SEVERE VON WILLEBRAND'S DISEASEKERNOFF LM; ROSE AG; HUGHES J et al.1981; THROMB. HAEMOST.; ISSN 0340-6245; DEU; DA. 1981; VOL. 46; PP. 714-716; BIBL. 10 REF.Article

LA MALADIE DE WILLEBRAND EN 1978SULTAN Y.1978; REV. MED.; FRA; DA. 1978; VOL. 19; NO 42; PP. 2362-2365; ABS. ENG; BIBL. 31 REF.Article

ACQUIRED VON WILLEBRAND'S DISEASE. EVIDENCE FOR A QUANTITATIVE AND QUALITATIVE FACTOR VIII DISORDER.JOIST JH; COWAN JF; ZIMMERMAN TS et al.1978; NEW ENGL. J. MED.; U.S.A.; DA. 1978; VOL. 298; NO 18; PP. 988-991; BIBL. 25 REF.Article

GERINNUNGSANALYTISCHE BEFUND BEIM VON-WILLEBRAND-SYNDROM = TESTS DE COAGULATION DANS LA MALADIE DE WILLEBRANDSCHONDORF TH; HEENE DL.1975; DTSCHE MED. WSCHR.; DTSCH.; DA. 1975; VOL. 100; NO 12; PP. 596-600; ABS. ANGL.Article

VON WILLEBRAND'S DISEASE IN GYNECOLOGIC AND OBSTETRIC PRACTICE = MALADIE DE VON WILLEBRAND DANS LA PRATIQUE GYNECOLOGIQUE ET OBSTETRIQUEPUGH M.1972; INTERNATION. J. GYNAECOL. OBSTETR.; U.S.A.; DA. 1972; VOL. 10; NO 4; PP. 137-143; ABS. FR.; BIBL. 4REF.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

VARIANT VON WILLEBRAND'S DISEASE TYPE B-REVISITEDHOWARD MA; SALEM HH; THOMAS KB et al.1982; BLOOD; ISSN 0006-4971; USA; DA. 1982; VOL. 60; NO 6; PP. 1420-1428; BIBL. 38 REF.Article

IMPAIRED FIBRINOLYTIC RESPONSE TO DDAVP AND VENOUS OCCLUSION IN A SUB-GROUP OF PATIENTS WITH VON WILLEBRAND'S DISEASEKORNINGER C; NIESSNER H; LECHNER K et al.1981; THROMB. RES.; ISSN 0049-3848; USA; DA. 1981; VOL. 23; NO 4-5; PP. 365-374; BIBL. 2 P.Article

TYPE IIB VON WILLEBRAND'S DISEASE: UNUSUAL RESPONSE TO CRYOPRECIPITATE INFUSIONWEINGER RS; CIMO PL; MOAKE JL et al.1981; ANN. INTERN. MED.; ISSN 0003-4819; USA; DA. 1981; VOL. 94; NO 1; PP. 47-50; BIBL. 31 REF.Article

CLASSIFICATION OF VON WILLEBRAND'S DISEASEINGRAM GIC.1978; LANCET; GBR; DA. 1978; NO 8104; PP. 1364-1365; BIBL. 29 REF.Article

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