AAAAAA

   
Results: 1-8 |
Results: 8
677C TO 677T MUTATION IN THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE(MTHFR) GENE AND PLASMA HOMOCYST(E)INE LEVELS IN PATIENTS WITH TIA ORMINOR STROKE
Authors: LALOUSCHEK W AULL S KORNINGER L MANNHALTER C PABINGERFASCHING I SCHMID RW SCHNIDER P ZEILER K
Citation: W. Lalouschek et al., 677C TO 677T MUTATION IN THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE(MTHFR) GENE AND PLASMA HOMOCYST(E)INE LEVELS IN PATIENTS WITH TIA ORMINOR STROKE, Journal of the neurological sciences, 155(2), 1998, pp. 156-162
EVALUATION OF A NEW SCREENING ASSAY PROC(R) GLOBAL FOR IDENTIFICATIONOF DEFECTS IN THE PROTEIN-C PROTEIN-S ANTICOAGULANT PATHWAY
Authors: RUZICKA K KAPIOTIS S QUEHENBERGER P HANDLER S PABINGERFASCHING I MANNHALTER C JILMA B SPEISER W
Citation: K. Ruzicka et al., EVALUATION OF A NEW SCREENING ASSAY PROC(R) GLOBAL FOR IDENTIFICATIONOF DEFECTS IN THE PROTEIN-C PROTEIN-S ANTICOAGULANT PATHWAY, Thrombosis research, 87(6), 1997, pp. 501-510
IS HYPERHOMOCYSTEINEMIA IN HEMODIALYSIS (HD) PATIENTS ASSOCIATED WITHA MUTATION OF THE METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) GENE
Authors: FODINGER M MANNHALTER C PABINGERFASCHING I HORL WH SUNDERPLASSMANN G
Citation: M. Fodinger et al., IS HYPERHOMOCYSTEINEMIA IN HEMODIALYSIS (HD) PATIENTS ASSOCIATED WITHA MUTATION OF THE METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) GENE, Journal of the American Society of Nephrology, 7(9), 1996, pp. 1817-1817
IMPROVED CHARACTERISTICS OF APC-RESISTANCE ASSAY - COATEST APC RESISTANCE BY PREDILUTION OF SAMPLES WITH FACTOR-V DEFICIENT PLASMA
Authors: KAPIOTIS S QUEHENBERGER P JILMA B HANDLER S PABINGERFASCHING I MANNHALTER C SPEISER W
Citation: S. Kapiotis et al., IMPROVED CHARACTERISTICS OF APC-RESISTANCE ASSAY - COATEST APC RESISTANCE BY PREDILUTION OF SAMPLES WITH FACTOR-V DEFICIENT PLASMA, American journal of clinical pathology, 106(5), 1996, pp. 588-593
CLINICAL AND LABORATORY DATA IN HETEROZYGOUS FACTOR-V LEIDEN MUTATIONPOSITIVE VERSUS NEGATIVE PATIENTS WITH TIA AND MINOR STROKE
Authors: LALOUSCHEK W SUESS E AULL S SCHNIDER P UHL F ZEILER K PABINGERFASCHING I
Citation: W. Lalouschek et al., CLINICAL AND LABORATORY DATA IN HETEROZYGOUS FACTOR-V LEIDEN MUTATIONPOSITIVE VERSUS NEGATIVE PATIENTS WITH TIA AND MINOR STROKE, Stroke, 26(10), 1995, pp. 1963-1964
SYMPTOMATIC HEREDITARY TYPE-II PROTEIN-C DEFICIENCY CAUSED BY A MISSENSE MUTATION IN EXON-IX OF THE PROTEIN-C GENE (GLY381 TO SER)
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
6 NOVEL AND 3 RECURRENT MUTATIONS IN 9 AUSTRIAN PATIENTS WITH HEMOPHILIA-B
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
RANDOMIZED DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF TWICE-DAILY ZIDOVUDINE IN ASYMPTOMATIC HEMOPHILIACS INFECTED WITH THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1
Authors: MANNUCCI PM GRINGERI A SAVIDGE G GATENBY P LAURIAN Y PABINGERFASCHING I MARTINEZVAZQUEZ JM HESSEY EW STEEL HM
Citation: Pm. Mannucci et al., RANDOMIZED DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL OF TWICE-DAILY ZIDOVUDINE IN ASYMPTOMATIC HEMOPHILIACS INFECTED WITH THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1, British Journal of Haematology, 86(1), 1994, pp. 174-179
Risultati: 1-8 |