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Results: 1-25 | 26-26
Results: 1-25/26
A NOVEL INSERTION MUTATION (1286INSC) IN EXON-9 OF THE FACTOR XIII-A SUBUNIT GENE
Authors: ASLAM S STANDEN GR BRUCE LJ GIALERAKI R MANDALAKI T
Citation: S. Aslam et al., A NOVEL INSERTION MUTATION (1286INSC) IN EXON-9 OF THE FACTOR XIII-A SUBUNIT GENE, Blood coagulation & fibrinolysis, 9(5), 1998, pp. 441-443
TYPE 2N VON-WILLEBRAND-DISEASE - RAPID GENETIC DIAGNOSIS OF G2811A (R854Q), C2696T (R816W), T2701A (H817Q) AND G2823T (C858F) - DETECTION OF A NOVEL CANDIDATE TYPE 2N MUTATION - C2810T (R854W)
Authors: BOWEN DJ STANDEN GR MAZURIER C GAUCHER C CUMMING A KEENEY S BIDWELL J
Citation: Dj. Bowen et al., TYPE 2N VON-WILLEBRAND-DISEASE - RAPID GENETIC DIAGNOSIS OF G2811A (R854Q), C2696T (R816W), T2701A (H817Q) AND G2823T (C858F) - DETECTION OF A NOVEL CANDIDATE TYPE 2N MUTATION - C2810T (R854W), Thrombosis and haemostasis, 80(1), 1998, pp. 32-36
A NEW (K1518E) CANDIDATE MUTATION DETECTED BY UNIVERSAL HETERODUPLEX GENERATOR ANALYSIS IN A PATIENT WITH TYPE 2A (PHENOTYPE IIA) VON-WILLEBRAND-DISEASE
Authors: ENAYAT MS THEOPHILUS BDM HILL FGH ROSE PE CULPAN D BIDWELL J STANDEN GR
Citation: Ms. Enayat et al., A NEW (K1518E) CANDIDATE MUTATION DETECTED BY UNIVERSAL HETERODUPLEX GENERATOR ANALYSIS IN A PATIENT WITH TYPE 2A (PHENOTYPE IIA) VON-WILLEBRAND-DISEASE, Thrombosis and haemostasis, 79(1), 1998, pp. 240-240
STRUCTURAL-ANALYSIS OF A MISSENSE MUTATION (VAL414PHE) IN THE CATALYTIC CORE DOMAIN OF THE FACTOR XIIIA SUBUNIT
Authors: ASLAM S YEE VC NARAYANAN S DURAISAMY G STANDEN GR
Citation: S. Aslam et al., STRUCTURAL-ANALYSIS OF A MISSENSE MUTATION (VAL414PHE) IN THE CATALYTIC CORE DOMAIN OF THE FACTOR XIIIA SUBUNIT, Thrombosis and haemostasis, 1997, pp. 3092-3092
GENETIC DIAGNOSIS OF FACTOR-V LEIDEN USING HETERODUPLEX TECHNOLOGY
Authors: BOWEN DJ STANDEN GR GRANVILLE S BOWLEY S WOOD NAP BIDWELL J
Citation: Dj. Bowen et al., GENETIC DIAGNOSIS OF FACTOR-V LEIDEN USING HETERODUPLEX TECHNOLOGY, Thrombosis and haemostasis, 77(1), 1997, pp. 119-122
RAPID DIAGNOSIS OF ASYMPTOMATIC HEREDITARY HEMOCHROMATOSIS BY DETECTION OF THE CYS282TYR MUTATION IN THE HLA-H GENE
Authors: ASLAM S STANDEN GR
Citation: S. Aslam et Gr. Standen, RAPID DIAGNOSIS OF ASYMPTOMATIC HEREDITARY HEMOCHROMATOSIS BY DETECTION OF THE CYS282TYR MUTATION IN THE HLA-H GENE, Postgraduate medical journal, 73(863), 1997, pp. 573-574
STRUCTURAL-ANALYSIS OF A MISSENSE MUTATION (VAL414PHE) IN THE CATALYTIC CORE DOMAIN OF THE FACTOR XIIIA SUBUNIT
Authors: ASLAM S YEE VC NARAYANAN S DURAISAMY G STANDEN GR
Citation: S. Aslam et al., STRUCTURAL-ANALYSIS OF A MISSENSE MUTATION (VAL414PHE) IN THE CATALYTIC CORE DOMAIN OF THE FACTOR XIIIA SUBUNIT, British Journal of Haematology, 98(2), 1997, pp. 346-352
GENETIC DETECTION OF FACTOR-V-LEIDEN - THE QUESTION OF SPECIFICITY
Authors: BOWEN DJ STANDEN GR
Citation: Dj. Bowen et Gr. Standen, GENETIC DETECTION OF FACTOR-V-LEIDEN - THE QUESTION OF SPECIFICITY, British Journal of Haematology, 97(3), 1997, pp. 691-692
IDENTIFICATION OF T-CELL EPITOPES ON THE RHESUS POLYPEPTIDES IN AUTOIMMUNE HEMOLYTIC-ANEMIA
Authors: BARKER RN HALL AM STANDEN GR JONES J ELSON CJ
Citation: Rn. Barker et al., IDENTIFICATION OF T-CELL EPITOPES ON THE RHESUS POLYPEPTIDES IN AUTOIMMUNE HEMOLYTIC-ANEMIA, Blood, 90(7), 1997, pp. 2701-2715
SHOULD PATIENTS WITH ATHEROSCLEROSIS OR PERIPHERAL VASCULAR-DISEASE BE STRATIFIED FOR FACTOR-V-LEIDEN
Authors: IRVINE CD FOLEY PWX STANDEN GR MORSE C
Citation: Cd. Irvine et al., SHOULD PATIENTS WITH ATHEROSCLEROSIS OR PERIPHERAL VASCULAR-DISEASE BE STRATIFIED FOR FACTOR-V-LEIDEN, Blood, 90(5), 1997, pp. 2114-2114
FACTOR-XIII(A) SUBUNIT DEFICIENCY DUE TO A HOMOZYGOUS 13-BASE PAIR DELETION IN EXON-3 OF THE A-SUBUNIT GENE
Authors: ASLAM S BOWEN DJ MANDALAKI T GIALERAKI R STANDEN GR
Citation: S. Aslam et al., FACTOR-XIII(A) SUBUNIT DEFICIENCY DUE TO A HOMOZYGOUS 13-BASE PAIR DELETION IN EXON-3 OF THE A-SUBUNIT GENE, American journal of hematology, 53(2), 1996, pp. 77-80
UHG-BASED MUTATION SCREENING IN TYPE 2B VON WILLEBRANDS DISEASE - DETECTION OF A CANDIDATE MUTATION SER547PHE
Authors: WOOD N STANDEN GR BOWEN DJ CUMMING A LUSH C LEE R BIDWELL J
Citation: N. Wood et al., UHG-BASED MUTATION SCREENING IN TYPE 2B VON WILLEBRANDS DISEASE - DETECTION OF A CANDIDATE MUTATION SER547PHE, Thrombosis and haemostasis, 75(2), 1996, pp. 363-367
EVALUATION OF A NEW, INTEGRAL, WHOLE-BLOOD FILTER (RS2000) SYSTEM FORPRESTORAGE LEUCODEPLETION OF SAG-M RED-CELLS
Authors: RIDER JR MOORE G PAYRAT JM CHAN D MORSE C STANDEN GR PAMPHILON DH
Citation: Jr. Rider et al., EVALUATION OF A NEW, INTEGRAL, WHOLE-BLOOD FILTER (RS2000) SYSTEM FORPRESTORAGE LEUCODEPLETION OF SAG-M RED-CELLS, British Journal of Haematology, 94(1), 1996, pp. 184-190
ACUTE PROMYELOCYTIC LEUKEMIA (M3) - RELAPSE WITH ACUTE MYELOBLASTIC-LEUKEMIA (M2) AND DIC(5-17) (Q11-P11)
Authors: HATZIS T STANDEN GR HOWELL RT SAVILL C WAGSTAFF M SCOTT GL
Citation: T. Hatzis et al., ACUTE PROMYELOCYTIC LEUKEMIA (M3) - RELAPSE WITH ACUTE MYELOBLASTIC-LEUKEMIA (M2) AND DIC(5-17) (Q11-P11), American journal of hematology, 48(1), 1995, pp. 40-44
MOLECULAR ANALYSIS IN FACTOR XIII(A) DEFICIENCY
Authors: ASLAM S STANDEN GR
Citation: S. Aslam et Gr. Standen, MOLECULAR ANALYSIS IN FACTOR XIII(A) DEFICIENCY, Thrombosis and haemostasis, 73(5), 1995, pp. 895-895
DVT FOLLOWING ORAL-CONTRACEPTIVE THERAPY IN ASSOCIATION WITH HOMOZYGOUS FACTOR-V LEIDEN
Authors: ASLAM S STANDEN GR MORSE C SCOTT GL
Citation: S. Aslam et al., DVT FOLLOWING ORAL-CONTRACEPTIVE THERAPY IN ASSOCIATION WITH HOMOZYGOUS FACTOR-V LEIDEN, Clinical and laboratory haematology, 17(1), 1995, pp. 99-100
PRESTORAGE WHITE CELL-REDUCTION IN SALINE-ADENINE-GLUCOSE-MANNITOL RED-CELLS BY USE OF AN INTEGRAL FILTER - EVALUATION OF STORAGE VALUES AND IN-VIVO RECOVERY
Authors: ROGERS SE EDMONDSON D GOODRICK MJ STANDEN GR FRANCK V REPPUCCI A PAMPHILON DH
Citation: Se. Rogers et al., PRESTORAGE WHITE CELL-REDUCTION IN SALINE-ADENINE-GLUCOSE-MANNITOL RED-CELLS BY USE OF AN INTEGRAL FILTER - EVALUATION OF STORAGE VALUES AND IN-VIVO RECOVERY, Transfusion, 35(9), 1995, pp. 727-733
FACTOR-XIII(A CALGARY) - A CANDIDATE MISSENSE MUTATION (LEU667PRO) INTHE BETA-BARREL 2 DOMAIN OF THE FACTOR-XIII(A) SUBUNIT
Authors: ASLAM S POON MC YEE VC BOWEN DJ STANDEN GR
Citation: S. Aslam et al., FACTOR-XIII(A CALGARY) - A CANDIDATE MISSENSE MUTATION (LEU667PRO) INTHE BETA-BARREL 2 DOMAIN OF THE FACTOR-XIII(A) SUBUNIT, British Journal of Haematology, 91(2), 1995, pp. 452-457
RAPID GENOTYPE ANALYSIS IN TYPE 2B VON WILLEBRANDS DISEASE USING A UNIVERSAL HETERODUPLEX GENERATOR
Authors: WOOD N STANDEN GR MURRAY EW LILLICRAP D HOLMBERG L PEAKE IR BIDWELL J
Citation: N. Wood et al., RAPID GENOTYPE ANALYSIS IN TYPE 2B VON WILLEBRANDS DISEASE USING A UNIVERSAL HETERODUPLEX GENERATOR, British Journal of Haematology, 89(1), 1995, pp. 152-156
HUMAN RH-D MONOCLONAL-ANTIBODIES (BRAD-3 AND BRAD-5) CAUSE ACCELERATED CLEARANCE OF RH-D-BLOOD-CELLS AND SUPPRESSION OF RH-D IMMUNIZATION IN RH-D- VOLUNTEERS( RED)
Authors: KUMPEL BM GOODRICK MJ PAMPHILON DH FRASER ID POOLE GD MORSE C STANDEN GR CHAPMAN GE THOMAS DP ANSTEE DJ
Citation: Bm. Kumpel et al., HUMAN RH-D MONOCLONAL-ANTIBODIES (BRAD-3 AND BRAD-5) CAUSE ACCELERATED CLEARANCE OF RH-D-BLOOD-CELLS AND SUPPRESSION OF RH-D IMMUNIZATION IN RH-D- VOLUNTEERS( RED), Blood, 86(5), 1995, pp. 1701-1709
FIRST REPORT ON UK DATABASE OF HEMOPHILIA-B MUTATIONS AND PEDIGREES
Authors: SAAD S ROWLEY G TAGLIAVACCA L GREEN PM GIANNELLI F RIZZA CR GLANGRANDE P KERNOFF PBA LEE C GOLDMAN E MCGRAW A COLVIN BT LUCAS G LAYTON M MIBASHAN RS PRESTON FE MAKRIS M MITCHELL VE LOWE GDO SAVIDGE GF HUNT BJ BAGLIN T GREEN A WHITMORE DN DUDLEY JM BEVAN D SCOTT GL STANDEN GR MAYNE EE WINTER P HILL FGH WILDE JT PRANGNELL DR JONES P DOLAN G STEVENS RF SUPER M ARONSTAM A WASSEF M BLOOM AL BOWEN DJ MONTGOMERY DA BOLTONMAGGS P HAYES JPLA LUDLAM CA GIBSON B HANN IM SWIRSKY DM SIMPSON CN DODD NJ TAYLOR G THOMPSON DS COPPLESTONE A CHISHOLM M WORSLEY A COSTELLO C LEE R TOLMIE J MCEVOY MW ROWLANDS M WINTER M LILLEYMAN JS OCONNOR N BEHRENS J OAKHILL A DALY HM PERRY DJ
Citation: S. Saad et al., FIRST REPORT ON UK DATABASE OF HEMOPHILIA-B MUTATIONS AND PEDIGREES, Thrombosis and haemostasis, 71(5), 1994, pp. 563-570
GENETIC-ANALYSIS IN A FEMALE MANIFESTING HEMOPHILIA-B
Authors: PALMER S STANDEN GR YATES P OAKHILL A
Citation: S. Palmer et al., GENETIC-ANALYSIS IN A FEMALE MANIFESTING HEMOPHILIA-B, Postgraduate medical journal, 70(829), 1994, pp. 828-829
AUTOIMMUNE NEUTROPENIA MANIFESTING AS RECURRENT ORAL ULCERATION
Authors: PORTER SR SCULLY C STANDEN GR
Citation: Sr. Porter et al., AUTOIMMUNE NEUTROPENIA MANIFESTING AS RECURRENT ORAL ULCERATION, Oral surgery, oral medicine, oral pathology, 78(2), 1994, pp. 178-180
TELOMERIC ASSOCIATIONS IN A PATIENT WITH B-CELL PROLYMPHOCYTIC LEUKEMIA
Authors: HOWELL RT KITCHEN C STANDEN GR
Citation: Rt. Howell et al., TELOMERIC ASSOCIATIONS IN A PATIENT WITH B-CELL PROLYMPHOCYTIC LEUKEMIA, Genes, chromosomes & cancer, 7(2), 1993, pp. 116-118
WISKOTT-ALDRICH SYNDROME - NO EVIDENCE OF CHROMOSOME INSTABILITY
Authors: THOMPSON P STANDEN GR
Citation: P. Thompson et Gr. Standen, WISKOTT-ALDRICH SYNDROME - NO EVIDENCE OF CHROMOSOME INSTABILITY, Cancer genetics and cytogenetics, 69(1), 1993, pp. 22-24
Risultati: 1-25 | 26-26