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Results: 1-15 |
Results: 15
DETECTION OF THE MOLECULAR LESIONS IN 29 FAMILIES WITH FACTOR-VII DEFICIENCY
Authors: PEYVANDI F MANNUCCI PM JENKINS PV PERRY DJ
Citation: F. Peyvandi et al., DETECTION OF THE MOLECULAR LESIONS IN 29 FAMILIES WITH FACTOR-VII DEFICIENCY, Thrombosis research, 91(3), 1998, pp. 6-6
A NOVEL POLYMORPHISM IN THE HUMAN FACTOR-VII GENE (IVS1A-VII LEVELS(9) IS ASSOCIATED WITH LOWER FACTOR)
Authors: PEYVANDI F MANNUCCI PM ZEINALI S AKHAVAN S BUCCIARELLI P PERRY DJ
Citation: F. Peyvandi et al., A NOVEL POLYMORPHISM IN THE HUMAN FACTOR-VII GENE (IVS1A-VII LEVELS(9) IS ASSOCIATED WITH LOWER FACTOR), Thrombosis research, 91(3), 1998, pp. 7-7
SPECTRUM OF THE CLINICAL MANIFESTATIONS OF INHERITED FACTOR-X DEFICIENCY IN 32 PATIENTS
Authors: PEYVANDI F MANNUCCI PM LAK M SHARIFIAN R PERRY DJ
Citation: F. Peyvandi et al., SPECTRUM OF THE CLINICAL MANIFESTATIONS OF INHERITED FACTOR-X DEFICIENCY IN 32 PATIENTS, Thrombosis research, 91(3), 1998, pp. 268-268
CONGENITAL FACTOR-X DEFICIENCY - SPECTRUM OF BLEEDING SYMPTOMS IN 32 IRANIAN PATIENTS
Authors: PEYVANDI F MANNUCCI PM LAK M ABDOULLAHI M ZEINALI S SHARIFIAN R PERRY D
Citation: F. Peyvandi et al., CONGENITAL FACTOR-X DEFICIENCY - SPECTRUM OF BLEEDING SYMPTOMS IN 32 IRANIAN PATIENTS, British Journal of Haematology, 102(2), 1998, pp. 626-628
CLINICAL MANIFESTATIONS OF INHERITED FACTOR-X DEFICIENCY IN 32 IRANIAN PATIENTS
Authors: PEYVANDI F MANNUCCI PM LAK M SHARIFIAN R PERRY DJ
Citation: F. Peyvandi et al., CLINICAL MANIFESTATIONS OF INHERITED FACTOR-X DEFICIENCY IN 32 IRANIAN PATIENTS, British Journal of Haematology, 102(1), 1998, pp. 137-137
IDENTIFICATION OF THE FACTOR-VII ARG4GLN MUTATION IN AN IRANIAN POPULATION WITH FACTOR-VII DEFICIENCY
Authors: PEYVANDI F MANNUCCI PM ABDOLLAHI M PERRY DJ BIANCHI A
Citation: F. Peyvandi et al., IDENTIFICATION OF THE FACTOR-VII ARG4GLN MUTATION IN AN IRANIAN POPULATION WITH FACTOR-VII DEFICIENCY, British Journal of Haematology, 102(1), 1998, pp. 137-137
LABORATORY DIAGNOSIS OF FACTOR-X DEFICIENCY
Authors: OWENS DL PEYVANDI F PERRY DJ
Citation: Dl. Owens et al., LABORATORY DIAGNOSIS OF FACTOR-X DEFICIENCY, British Journal of Haematology, 102(1), 1998, pp. 261-261
IDENTIFICATION OF THE FACTOR-VII ARG304GLN MUTATION IN AN IRANIAN POPULATION WITH FACTOR-VII DEFICIENCY
Authors: PEYVANDI F MANNUCCI PM ABDOLLAHI M PERRY DJ
Citation: F. Peyvandi et al., IDENTIFICATION OF THE FACTOR-VII ARG304GLN MUTATION IN AN IRANIAN POPULATION WITH FACTOR-VII DEFICIENCY, British Journal of Haematology, 101, 1998, pp. 261-261
CLINICAL MANIFESTATIONS OF INHERITED FACTOR-X DEFICIENCY IN 32 IRANIAN PATIENTS
Authors: PEYVANDI F MANNUCCI PM LAK M SHARIFIAN R PERRY DJ
Citation: F. Peyvandi et al., CLINICAL MANIFESTATIONS OF INHERITED FACTOR-X DEFICIENCY IN 32 IRANIAN PATIENTS, British Journal of Haematology, 101, 1998, pp. 262-262
BLEEDING SYMPTOMS IN 27 IRANIAN PATIENTS WITH THE COMBINED DEFICIENCYOF FACTOR-V AND FACTOR-VIII
Authors: PEYVANDI F TUDDENHAM EGD AKHTARI AM LAK M MANNUCCI PM
Citation: F. Peyvandi et al., BLEEDING SYMPTOMS IN 27 IRANIAN PATIENTS WITH THE COMBINED DEFICIENCYOF FACTOR-V AND FACTOR-VIII, British Journal of Haematology, 100(4), 1998, pp. 773-776
CLINICAL MANIFESTATIONS IN 28 ITALIAN AND IRANIAN PATIENTS WITH SEVERE FACTOR-VII DEFICIENCY
Authors: PEYVANDI F MANNUCCI PM ASTI D ABDOULLAHI M DIROCCO N SHARIFIAN R
Citation: F. Peyvandi et al., CLINICAL MANIFESTATIONS IN 28 ITALIAN AND IRANIAN PATIENTS WITH SEVERE FACTOR-VII DEFICIENCY, Haemophilia, 3(4), 1997, pp. 242-246
GENE POLYMORPHISMS PREDICTING HIGH PLASMA-LEVELS OF COAGULATION AND FIBRINOLYSIS PROTEINS - A STUDY IN CENTENARIANS
Authors: MANNUCCI PM MARI D MERATI G PEYVANDI F TAGLIABUE L SACCHI E TAIOLI E SANSONI P BERTOLINI S FRANCESCHI C
Citation: Pm. Mannucci et al., GENE POLYMORPHISMS PREDICTING HIGH PLASMA-LEVELS OF COAGULATION AND FIBRINOLYSIS PROTEINS - A STUDY IN CENTENARIANS, Arteriosclerosis, thrombosis, and vascular biology, 17(4), 1997, pp. 755-759
THE G(1456) TO T-MUTATION IN THE THROMBOMODULIN GENE IS NOT FREQUENT IN PATIENTS WITH VENOUS THROMBOSIS
Authors: FAIONI EM MERATI G PEYVANDI F BETTINI PM MANNUCCI PM
Citation: Em. Faioni et al., THE G(1456) TO T-MUTATION IN THE THROMBOMODULIN GENE IS NOT FREQUENT IN PATIENTS WITH VENOUS THROMBOSIS, Blood, 89(4), 1997, pp. 1467-1467
FACTOR-V (ARG(506)-]GLN) MUTATION IN YOUNG SURVIVORS OF MYOCARDIAL-INFARCTION
Authors: ARDISSINO D PEYVANDI F MERLINI PA COLOMBI E MANNUCCI PM
Citation: D. Ardissino et al., FACTOR-V (ARG(506)-]GLN) MUTATION IN YOUNG SURVIVORS OF MYOCARDIAL-INFARCTION, Thrombosis and haemostasis, 75(5), 1996, pp. 701-702
FREQUENCY OF FACTOR-V ARG506 GLN IN ITALIANS
Authors: MANNUCCI PM DUCA F PEYVANDI F TAGLIABUE L MERATI G MARTINELLI I CATTANEO M
Citation: Pm. Mannucci et al., FREQUENCY OF FACTOR-V ARG506 GLN IN ITALIANS, Thrombosis and haemostasis, 75(4), 1996, pp. 694-694
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