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Results:
1-13
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Results: 13
Authors:
NOBAUERHUHMANN IM
HOLLER W
KRINNINGER B
TURECEK PL
RICHTER G
SCHARRER I
FORBERG E
WATZKE HH
Citation: Im. Nobauerhuhmann et al., FACTOR-X FRANKFURT-I - MOLECULAR AND FUNCTIONAL-CHARACTERIZATION OF AHEREDITARY FACTOR-X DEFICIENCY (GLA(+25) TO LYS), Blood coagulation & fibrinolysis, 9(2), 1998, pp. 143-152
Authors:
HUHMANN I
HOFBAUER E
FORBERG E
WATZKE HH
WATZKE IM
Citation: I. Huhmann et al., ELEVATED ACTIVATION MARKERS OF COAGULATION IN PATIENTS UNDERGOING ORTHOGNATHIC SURGERY, International journal of oral and maxillofacial surgery, 27(5), 1998, pp. 374-376
Authors:
ROSENDAAL FR
DOGGEN CJM
ZIVELIN A
ARRUDA VR
AIACH M
SISCOVICK DS
HILLARP A
WATZKE HH
BERNARDI F
CUMMING AM
PRESTON FE
REITSMA PH
Citation: Fr. Rosendaal et al., GEOGRAPHIC-DISTRIBUTION OF THE 20210-G TO 20210-A PROTHROMBIN VARIANT, Thrombosis and haemostasis, 79(4), 1998, pp. 706-708
Authors:
WATZKE HH
SCHUTTRUMPF J
PANZER S
GRAF S
HUBER K
Citation: Hh. Watzke et al., DISTRIBUTION OF THE G A POLYMORPHISM IN PROTHROMBIN IN PATIENTS WITH PREMATURE CORONARY HEART-DISEASE AND MYOCARDIAL-INFARCTION/, Thrombosis and haemostasis, 1997, pp. 1550-1550
Authors:
HUHMANN I
TURECEK PL
RICHTER G
SCHARRER I
FORBERG E
WATZKE HH
Citation: I. Huhmann et al., FACTOR-X FRANKFURT-I - MOLECULAR CHARACTERIZATION AND IN-VITRO EXPRESSION OF A HEREDITARY FACTOR-X DEFECT (GLA+25 TO LYS), Thrombosis and haemostasis, 1997, pp. 1743-1743
Authors:
WATZKE HH
SCHUTTRUMPF J
GRAF S
HUBER K
PANZER S
Citation: Hh. Watzke et al., INCREASED PREVALENCE OF A POLYMORPHISM IN THE GENE CODING FOR HUMAN PROTHROMBIN IN PATIENTS WITH CORONARY HEART-DISEASE, Thrombosis research, 87(6), 1997, pp. 521-526
Authors:
HUHMANN IM
WATZKE HH
GEISSLER K
GISSLINGER H
JAGER U
KNOBL P
PABINGER I
KORNINGER L
MANNHALTER C
MITTERBAUER G
SCHWARZINGER I
KALHS P
HAAS OA
LECHNER K
Citation: Im. Huhmann et al., FLAG (FLUDARABINE, CYTOSINE-ARABINOSIDE, G-CSF) FOR REFRACTORY AND RELAPSED ACUTE MYELOID-LEUKEMIA, Annals of hematology, 73(6), 1996, pp. 265-271
Authors:
FORBERG E
HUHMANN I
WATZKE HH
Citation: E. Forberg et al., CHARACTERIZATION OF THE FUNCTIONAL FACTOR-X DEFECT RESULTING FROM THESUBSTITUTION OF LYS FOR GLU102, Blood, 88(10), 1996, pp. 2989-2989
Authors:
HUHMANN I
TURECEK PL
RICHTER G
SCHARRER I
FORBERG E
WATZKE HH
Citation: I. Huhmann et al., FACTOR-X FRANKFURT-I - MOLECULAR CHARACTERIZATION AND IN-VITRO EXPRESSION OF A HEREDITARY FACTOR-X DEFECT (GLA+25 TO LYS), Blood, 88(10), 1996, pp. 2994-2994
Authors:
WITTMANN E
WALTER J
PABINGERFASCHING I
WATZKE HH
Citation: E. Wittmann et al., SYMPTOMATIC HEREDITARY TYPE-II PROTEIN-C DEFICIENCY CAUSED BY A MISSENSE MUTATION IN EXON-IX OF THE PROTEIN-C GENE (GLY381 TO SER), Annals of hematology, 68(5), 1994, pp. 255-259
Authors:
WALTER J
PABINGERFASCHING I
WATZKE HH
Citation: J. Walter et al., 6 NOVEL AND 3 RECURRENT MUTATIONS IN 9 AUSTRIAN PATIENTS WITH HEMOPHILIA-B, Thrombosis and haemostasis, 72(1), 1994, pp. 74-77
Authors:
WATZKE HH
LECHNER K
LARSON P
HIGH KA
Citation: Hh. Watzke et al., FACTOR-XVIENNA MOLECULAR ANALYSIS AND IN-VITRO EXPRESSION OF A SEVERECRM(-) FX DEFICIENCY, Thrombosis and haemostasis, 69(6), 1993, pp. 752-752
Authors:
WALTER J
KRINNINGER B
WATZKE HH
Citation: J. Walter et al., CHARACTERIZATION OF THE GENETIC-DEFECTS IN 6 UNRELATED PATIENTS WITH HEMOPHILIA-B, Thrombosis and haemostasis, 69(6), 1993, pp. 848-848
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