EPA CONTENT: A CRITERION OF QUALITY FOR PLASMA AS FACTOR VIII SOURCEPFLUGSHAUPT R; KURT G.1983; VOX SANGUINIS; ISSN 0042-9007; CHE; DA. 1983; VOL. 45; NO 3; PP. 224-232; BIBL. 16 REF.Article

HUMAN RED CELL GLYOXALASE I POLYMORPHISM IN THE SWISS POPULATION: PHENOTYPE FREQUENCIES AND A SIMPLIFIED TECHNIQUE.PFLUGSHAUPT R; SCHERZ R; BUTLER R et al.1978; HUM. HERED.; SWITZ.; DA. 1978; VOL. 28; NO 3; PP. 235-237; BIBL. 11 REF.Article

POLYMORPHISM OF HUMAN RED CELL ADENOSINE DEAMINASE, ESTERASE D, GLUTAMATE PYRUVATE TRANSAMINASE AND GALACTOSE-1-PHOSPHATE-URIDYLTRANSFERASE IN THE SWISS POPULATION.PFLUGSHAUPT R; SCHERZ R; BUTLER R et al.1976; HUM. HERED.; SWITZ.; DA. 1976; VOL. 26; NO 3; PP. 161-166; BIBL. 1 P. 1/2Article

ERWORBENER ISOLIERTER FAKTOR-X-DEFEKT BEI GENERALISIERTER AMYLOIDOSE = UN DEFAUT ISOLE ACQUIS EN FACTEURX DANS L'AMYLOIDOSE GENERALISEEWICK A; SULSER H; PFLUGSHAUPT R et al.1972; SCHWEIZ. MED. WSCHR.,; SCHWEIZ; DA. 1972; VOL. 102; NO 48; PP. 1760-1766; ABS. ANGL.Serial Issue

ISOELECTRIC FOCUSING OF HUMAN RED CELL PHOSPHOGLUCOMUTASE (PGM₁): PHENOTYPE DISTRIBUTION IN THE SWISS POPULATION, RARE PHENOTYPESSCHERZ R; PFLUGSHAUPT R; BUETLER R et al.1981; HUM. HERED.; ISSN 0001-5652; CHE; DA. 1981; VOL. 31; NO 3; PP. 187-190; BIBL. 9 REF.Article

A NEW RARE PHENOTYPE OF GLYCINE-RICH BETA -GLYCOPROTEINSCHERZ R; PFLUGSHAUPT R; BUTLER R et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 45; NO 1; PP. 81-83; BIBL. 7 REF.Article

GENETIC POLYMORPHISM OF GLYCINE-RICH BETA -GLYCOPROTEIN IN THE SWISS AND ITALIAN POPULATIONS.SCHERZ R; PFLUGSHAUPT R; BUTLER R et al.1977; HUM. HERED.; SWITZ.; DA. 1977; VOL. 27; NO 2; PP. 143-146; BIBL. 8 REF.Article

NATURALLY OCCURING HUMAN ANTIBODIES WITH SPECIFICITY FOR LIGHT CHAINS OF IMMUNOGLOBULINS.SCHERZ R; PFLUGSHAUPT R; BUTLER R et al.1977; VOX SANG.; SUISSE; DA. 1977; VOL. 32; NO 2; PP. 69-76; BIBL. 22 REF.Article

A NEW GENETIC VARIANT OF GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE.SCHERZ R; PFLUGSHAUPT R; BUTLER R et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 35; NO 1; PP. 51-55; BIBL. 11 REF.Article

GENETIC POLYMORPHISM OF GLYCINE-RICH BETA-GLYCOPROTEIN IN THE ITALIAN POPULATIONSCHERZ R; PFLUGSHAUPT R; BUETLER R et al.1982; HUM. HERED.; ISSN 0001-5652; CHE; DA. 1982; VOL. 32; NO 1; PP. 11-14; BIBL. 10 REF.Article

HETEROZYGOTENERFASSUNG BEI DER HAEMOPHILIE A. GENEALOGISCHE UND BIOCHEMISCHE RESULTATE EINER FELDSTUDIE AN 25 BLUTERFAMILIEN = HEMOPATHIE A. HETEROZYGOTIE. RESULTATTS D'UNE ETUDE BIOCHIMIQUE ET GENETIQUE DE 25 MALADES D'HAMATOLOGIEHINDERBERGER P; MOSER H; BECK EA et al.1980; PRAXIS; ISSN 0369-8394; CHE; DA. 1980; VOL. 69; NO 38; PP. 1343-1360; ABS. ENG/FRE; BIBL. 38 REF.Article

TRANSCOBALAMIN II POLYMORPHISM IN THE SWISS POPULATION - ITS APPLICATION IN PATERNITY TESTINGSCHERZ R; FRATER SCHROEDER M; STEINEGGER L et al.1982; HUMAN HEREDITY; ISSN 0001-5652; CHE; DA. 1982; VOL. 32; NO 4; PP. 289-292; BIBL. 10 REF.Article

Multimetric analysis of von Willebrand factor by vertical sodium dodecyl sulphate agarose gel electrophoresis, vacuum blotting technology and sensitive visualization by alkaline phosphatase anti-alkaline phosphatase complexBAILLOD, P; AFFOLTER, B; KURT, G. H et al.Thrombosis research. 1992, Vol 66, Num 6, pp 745-755, issn 0049-3848Article

New variant of type II von Willebrand's disease with structural abnormality of plasma von Willebrand factor in a patient with very mild bleeding historyBAILLOD, P; GAUCHER, C; AFFOLTER, B et al.American journal of hematology. 1995, Vol 49, Num 1, pp 21-28, issn 0361-8609Article

Thromboembolism and bleeding tendency in congenital factor XII deficiency : a study on 74 subjects from 14 Swiss familiesLÄMMLE, B; WUILLEMIN, W. A; HUBER, I et al.Thrombosis and haemostasis. 1991, Vol 65, Num 2, pp 117-121, issn 0340-6245Article