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Results: 1-9 |
Results: 9
THE HETEROZYGOUS-20210 G A PROTHROMBIN GENOTYPE IS ASSOCIATED WITH EARLY VENOUS THROMBOSIS IN INHERITED THROMBOPHILIAS AND IS NOT INCREASEDIN FREQUENCY IN ARTERY DISEASE/
Authors: FERRARESI P MARCHETTI G LEGNANI C CAVALLARI E CASTOLDI E MASCOLI F ARDISSINO D PALARETI G BERNARDI F
Citation: P. Ferraresi et al., THE HETEROZYGOUS-20210 G A PROTHROMBIN GENOTYPE IS ASSOCIATED WITH EARLY VENOUS THROMBOSIS IN INHERITED THROMBOPHILIAS AND IS NOT INCREASEDIN FREQUENCY IN ARTERY DISEASE/, Arteriosclerosis, thrombosis, and vascular biology, 17(11), 1997, pp. 2418-2422
HYPERHOMOCYST(E)INEMIA AND A COMMON METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION (ALA(223)VAL MTHFR) IN PATIENTS WITH INHERITED THROMBOPHILIC COAGULATION DEFECTS
Authors: LEGNANI C PALARETI G GRAUSO F SASSI S GROSSI G PIAZZI S BERNARDI F MARCHETTI G FERRARESI P COCCHERI S
Citation: C. Legnani et al., HYPERHOMOCYST(E)INEMIA AND A COMMON METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION (ALA(223)VAL MTHFR) IN PATIENTS WITH INHERITED THROMBOPHILIC COAGULATION DEFECTS, Arteriosclerosis, thrombosis, and vascular biology, 17(11), 1997, pp. 2924-2929
VISUAL CONTROL OF HAND-REACHING MOVEMENT - ACTIVITY IN PARIETAL AREA 7M
Authors: FERRAINA S GARASTO MR BATTAGLIAMAYER A FERRARESI P JOHNSON PB LACQUANITI F CAMINITI R
Citation: S. Ferraina et al., VISUAL CONTROL OF HAND-REACHING MOVEMENT - ACTIVITY IN PARIETAL AREA 7M, European journal of neuroscience, 9(5), 1997, pp. 1090-1095
STUDY OF A G A VARIATION IN THE 3'-UNTRANSLATED REGION OF PROTHROMBINMESSENGER-RNA IN ITALIAN PATIENTS WITH VENOUS THROMBOSIS/
Authors: FERRARESI P LEGNANI C QUAGLIO S CASTOLDI E MARCHETTI G PALARETI G BERNARDI F
Citation: P. Ferraresi et al., STUDY OF A G A VARIATION IN THE 3'-UNTRANSLATED REGION OF PROTHROMBINMESSENGER-RNA IN ITALIAN PATIENTS WITH VENOUS THROMBOSIS/, Thrombosis and haemostasis, 1997, pp. 1547-1547
A FAMILY STUDY OF FVII GENOTYPE, ELEVATED LEVELS OF FACTOR-VII AND ARTERIAL THROMBOTIC DISEASE
Authors: CASTAMAN G FERRARESI P RUGGIERI M BERNARDI F MARCHETTI G
Citation: G. Castaman et al., A FAMILY STUDY OF FVII GENOTYPE, ELEVATED LEVELS OF FACTOR-VII AND ARTERIAL THROMBOTIC DISEASE, Thrombosis and haemostasis, 1997, pp. 1682-1682
ANGIOTENSIN-CONVERTING ENZYME GENE POLYMORPHISM AND RISK OF RESTENOSIS AFTER CORONARY STENTING
Authors: BARBERIS P MERLINI PA CAVALOTTI C BERNARDI F MARCHETTI G FERRARESI P LAUDISA ML ARDISSINO D
Citation: P. Barberis et al., ANGIOTENSIN-CONVERTING ENZYME GENE POLYMORPHISM AND RISK OF RESTENOSIS AFTER CORONARY STENTING, Thrombosis and haemostasis, 1997, pp. 2125-2125
HYPERHOMOCYST(E)INEMIA AND A COMMON METHYLENE-TETRAHYDROFOLATE REDUCTASE MUTATION (ALA223 VAL MTHFR) ARE NOT ASSOCIATED WITH A HISTORY OF THROMBOSIS IN PATIENTS WITH INHERITED THROMBOPHILIA
Authors: LEGNANI C PALARETI G SASSI S GRAUSO F BARGOSSI A BERNARDI F MARCHETTI G FERRARESI P COCCHERI S
Citation: C. Legnani et al., HYPERHOMOCYST(E)INEMIA AND A COMMON METHYLENE-TETRAHYDROFOLATE REDUCTASE MUTATION (ALA223 VAL MTHFR) ARE NOT ASSOCIATED WITH A HISTORY OF THROMBOSIS IN PATIENTS WITH INHERITED THROMBOPHILIA, Thrombosis and haemostasis, 1997, pp. 2325-2325
MUTATION PATTERN IN CLINICALLY ASYMPTOMATIC COAGULATION-FACTOR-VII DEFICIENCY
Authors: BERNARDI F CASTAMAN G PINOTTI M FERRARESI P DIIASIO MG LUNGHI B RODEGHIERO F MARCHETTI G
Citation: F. Bernardi et al., MUTATION PATTERN IN CLINICALLY ASYMPTOMATIC COAGULATION-FACTOR-VII DEFICIENCY, Human mutation, 8(2), 1996, pp. 108-115
A HEPARIN-COFACTOR-II MUTATION (HCII RIMINI) COMBINED WITH FACTOR-V LEIDEN OR TYPE-I PROTEIN-C DEFICIENCY IN 2 UNRELATED THROMBOPHILIC SUBJECTS
Authors: BERNARDI F LEGNANI C MICHELETTI F LUNGHI B FERRARESI P PALARETI G BIAGI R MARCHETTI G
Citation: F. Bernardi et al., A HEPARIN-COFACTOR-II MUTATION (HCII RIMINI) COMBINED WITH FACTOR-V LEIDEN OR TYPE-I PROTEIN-C DEFICIENCY IN 2 UNRELATED THROMBOPHILIC SUBJECTS, Thrombosis and haemostasis, 76(4), 1996, pp. 505-509
Risultati: 1-9 |