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Results: 1-25 | 26-50 | 51-53
Results: 1-25/53
ALPHA-ANTITRYPSIN DEFICIENCY ALLELES AND THE TAQ-I G-]A ALLELE IN CYSTIC-FIBROSIS LUNG-DISEASE
Authors: MAHADEVA R WESTERBEEK RC PERRY DJ LOVEGROVE JU WHITEHOUSE DB CARROLL NR ROSSRUSSELL RI WEBB AK BILTON D LOMAS DA
Citation: R. Mahadeva et al., ALPHA-ANTITRYPSIN DEFICIENCY ALLELES AND THE TAQ-I G-]A ALLELE IN CYSTIC-FIBROSIS LUNG-DISEASE, The European respiratory journal, 11(4), 1998, pp. 873-879
ANTITHROMBIN CAMBRIDGE-II (ALA384SER) - CLINICAL, FUNCTIONAL AND HAPLOTYPE ANALYSIS OF 18 FAMILIES
Authors: PERRY DJ DALY ME TAIT RC WALKER ID BROWN K BEAUCHAMP NJ PRESTON FE GYDE H HARPER PL CARRELL RW
Citation: Dj. Perry et al., ANTITHROMBIN CAMBRIDGE-II (ALA384SER) - CLINICAL, FUNCTIONAL AND HAPLOTYPE ANALYSIS OF 18 FAMILIES, Thrombosis and haemostasis, 79(2), 1998, pp. 249-253
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
SEQUENCE-TAGGED-SITE (STS) MARKERS OF ARBITRARY GENES - THE UTILITY OF BLACK SPRUCE-DERIVED STS PRIMERS IN OTHER CONIFERS
Authors: PERRY DJ BOUSQUET J
Citation: Dj. Perry et J. Bousquet, SEQUENCE-TAGGED-SITE (STS) MARKERS OF ARBITRARY GENES - THE UTILITY OF BLACK SPRUCE-DERIVED STS PRIMERS IN OTHER CONIFERS, Theoretical and Applied Genetics, 97(5-6), 1998, pp. 735-743
SEQUENCE-TAGGED-SITE (STS) MARKERS OF ARBITRARY GENES - DEVELOPMENT, CHARACTERIZATION AND ANALYSIS OF LINKAGE IN BLACK SPRUCE
Authors: PERRY DJ BOUSQUET J
Citation: Dj. Perry et J. Bousquet, SEQUENCE-TAGGED-SITE (STS) MARKERS OF ARBITRARY GENES - DEVELOPMENT, CHARACTERIZATION AND ANALYSIS OF LINKAGE IN BLACK SPRUCE, Genetics, 149(2), 1998, pp. 1089-1098
THROMBELASTOGRAPHY - AN EFFECTIVE SCREENING-TEST FOR PROTHROMBOTIC STATES
Authors: HANDA K COX DL PASI KJ PERRY DJ HAMILTON G
Citation: K. Handa et al., THROMBELASTOGRAPHY - AN EFFECTIVE SCREENING-TEST FOR PROTHROMBOTIC STATES, British Journal of Surgery, 85(11), 1998, pp. 1560-1560
THROMBOELASTOGRAPHY - AN EFFECTIVE SCREENING-TEST FOR PROTHROMBOTIC STATES
Authors: HANDA A COX DJ PASI KJ PERRY DJ HAMILTON G
Citation: A. Handa et al., THROMBOELASTOGRAPHY - AN EFFECTIVE SCREENING-TEST FOR PROTHROMBOTIC STATES, British Journal of Surgery, 85, 1998, pp. 90-90
DIAGNOSIS AND RECLASSIFICATION OF TYPE-1 VONWILLEBRAND-DISEASE (VWD) - INFLUENCE OF ABO BLOOD-GROUP
Authors: NITU IC PASI KJ PERRY DJ LEE CA
Citation: Ic. Nitu et al., DIAGNOSIS AND RECLASSIFICATION OF TYPE-1 VONWILLEBRAND-DISEASE (VWD) - INFLUENCE OF ABO BLOOD-GROUP, British Journal of Haematology, 102(1), 1998, pp. 16-16
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
CLINICAL-EXPERIENCE WITH USE OF CLOTTING FACTOR CONCENTRATE IN ORAL ANTICOAGULATION REVERSAL - AN AUDIT
Authors: NITU IC PASI KJ PERRY DJ LEE CA
Citation: Ic. Nitu et al., CLINICAL-EXPERIENCE WITH USE OF CLOTTING FACTOR CONCENTRATE IN ORAL ANTICOAGULATION REVERSAL - AN AUDIT, British Journal of Haematology, 102(1), 1998, pp. 265-265
DISORDERED FIBRINOLYSIS IN KLINEFELTERS-SYNDROME
Authors: ANGUS G HARRINGTON C OWENS D BOULOUX P PERRY DJ
Citation: G. Angus et al., DISORDERED FIBRINOLYSIS IN KLINEFELTERS-SYNDROME, British Journal of Haematology, 102(1), 1998, pp. 268-268
DISORDERED FIBRINOLYSIS IN KLINEFELTERS-SYNDROME
Authors: ANGUS G HARRINGTON C OWENS D BOULOUX P PERRY DJ
Citation: G. Angus et al., DISORDERED FIBRINOLYSIS IN KLINEFELTERS-SYNDROME, British Journal of Haematology, 101, 1998, pp. 220-220
DIAGNOSIS AND RECLASSIFICATION OF TYPE-1 VWD - INFLUENCE OF ABO BLOOD-GROUP
Authors: NITU IC LEE CA PERRY DJ PASI KJ
Citation: Ic. Nitu et al., DIAGNOSIS AND RECLASSIFICATION OF TYPE-1 VWD - INFLUENCE OF ABO BLOOD-GROUP, British Journal of Haematology, 101, 1998, pp. 253-253
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
RESISTANCE TO ACTIVATED PROTEIN-C AND FACTOR-V-LEIDEN
Authors: PERRY DJ PASI KJ
Citation: Dj. Perry et Kj. Pasi, RESISTANCE TO ACTIVATED PROTEIN-C AND FACTOR-V-LEIDEN, Quarterly Journal of Medicine, 90(6), 1997, pp. 379-385
BOVINE GRANULOCYTE CHEMOTACTIC PROTEIN-2 IS SECRETED BY THE ENDOMETRIUM IN RESPONSE TO INTERFERON-TAU (IFN-TAU)
Authors: TEIXEIRA MG AUSTIN KJ PERRY DJ DOOLEY VD JOHNSON GA FRANCIS BR HANSEN TR
Citation: Mg. Teixeira et al., BOVINE GRANULOCYTE CHEMOTACTIC PROTEIN-2 IS SECRETED BY THE ENDOMETRIUM IN RESPONSE TO INTERFERON-TAU (IFN-TAU), Endocrine, 6(1), 1997, pp. 31-37
FACTOR-X AND ITS DEFICIENCY STATES
Authors: PERRY DJ
Citation: Dj. Perry, FACTOR-X AND ITS DEFICIENCY STATES, Haemophilia, 3(3), 1997, pp. 159-172
RECURRENT VENOUS THROMBOEMBOLIC DISEASE AND FACTOR-XI CONCENTRATE IN A PATIENT WITH SEVERE FACTOR-XI DEFICIENCY, CHRONIC MYELOMONOCYTIC LEUKEMIA, FACTOR-V-LEIDEN AND HETEROZYGOUS PLASMINOGEN DEFICIENCY
Authors: EVANS G PASI KJ MEHTA A LEE CA PERRY DJ
Citation: G. Evans et al., RECURRENT VENOUS THROMBOEMBOLIC DISEASE AND FACTOR-XI CONCENTRATE IN A PATIENT WITH SEVERE FACTOR-XI DEFICIENCY, CHRONIC MYELOMONOCYTIC LEUKEMIA, FACTOR-V-LEIDEN AND HETEROZYGOUS PLASMINOGEN DEFICIENCY, Blood coagulation & fibrinolysis, 8(7), 1997, pp. 437-440
ASYMPTOMATIC COINHERITANCE OF HETEROZYGOUS PLASMINOGEN DEFICIENCY ANDTHE FACTOR-V-LEIDEN MUTATION
Authors: MCCOLL MD TAIT RC WALKER ID MCCALL F CONKIE JA PERRY DJ
Citation: Md. Mccoll et al., ASYMPTOMATIC COINHERITANCE OF HETEROZYGOUS PLASMINOGEN DEFICIENCY ANDTHE FACTOR-V-LEIDEN MUTATION, Blood coagulation & fibrinolysis, 8(3), 1997, pp. 195-199
A COMMON MUTATION IN THE ANTITHROMBIN GENE - ALA384SER - CLINICAL, FUNCTIONAL AND HAPLOTYPE ANALYSIS OF 18 FAMILIES
Authors: PERRY DJ DALY ME TAIT RC WALKER ID BROWN K BEAUCHAMP NJ PRESTON FE GYDE H HARPER PL CARRELL RW
Citation: Dj. Perry et al., A COMMON MUTATION IN THE ANTITHROMBIN GENE - ALA384SER - CLINICAL, FUNCTIONAL AND HAPLOTYPE ANALYSIS OF 18 FAMILIES, Thrombosis and haemostasis, 1997, pp. 766-766
Risultati: 1-25 | 26-50 | 51-53