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Results: 1-11 |
Results: 11

Authors: TOMLINSON IPM BECK NE WILLIAMSON J HAROCOPOS CJ MITCHELL VE HODGSON SV BODMER WF
Citation: Ipm. Tomlinson et al., CLINICAL-FEATURES AND MOLECULAR ANALYSIS OF A FAMILY WITH MULTIPLE COLON TUMORS AND REDUCED PLASMINOGEN-ACTIVATOR ACTIVITY, International journal of colorectal disease, 12(1), 1997, pp. 1-3

Authors: ALDRED MA SPENCE L MITCHELL VE
Citation: Ma. Aldred et al., DETECTION OF KNOWN MUTATIONS - TOWARDS PARALLEL-PROCESSING IN THE DIAGNOSTIC LABORATORY, American journal of human genetics, 61(4), 1997, pp. 1254-1254

Authors: PAVORD SR MURPHY PT MITCHELL VE
Citation: Sr. Pavord et al., POEMS SYNDROME AND WALDENSTROMS MACROGLOBULINEMIA, Journal of Clinical Pathology, 49(2), 1996, pp. 181-182

Authors: MURPHY PT CASEY MC MITCHELL VE
Citation: Pt. Murphy et al., AUDIT OF PATIENTS ON ORAL ANTICOAGULATION WITH INRS OF 8 OR ABOVE - CAUSES AND MANAGEMENT, British Journal of Haematology, 93, 1996, pp. 219-219

Authors: SIVAKUMARAN M SWANN RA MITCHELL VE QURESHI H WOOD JK
Citation: M. Sivakumaran et al., THERAPEUTIC EFFICACY OF AMBISOME - A CAUTIONARY NOTE, American journal of hematology, 48(3), 1995, pp. 208-209

Authors: DREYFUS M MASTERSON M DAVID M RIVARD GE MULLER FM KREUZ W BEEG T MINFORD A ALLGROVE J BERGMANN F MITCHELL VE HAWORTH C NELSON K SCHWARZ HP
Citation: M. Dreyfus et al., REPLACEMENT THERAPY WITH A MONOCLONAL-ANTIBODY PURIFIED PROTEIN-C CONCENTRATE IN NEWBORNS WITH SEVERE CONGENITAL PROTEIN-C DEFICIENCY, Seminars in thrombosis and hemostasis, 21(4), 1995, pp. 371-381

Authors: MURPHY PT SIVAKUMARAN M VANRHEE F WATMORE AE MITCHELL VE
Citation: Pt. Murphy et al., ACUTE LYMPHOBLASTIC TRANSFORMATION OF ESSENTIAL THROMBOCYTHEMIA, British Journal of Haematology, 89(4), 1995, pp. 921-922

Authors: DUNN ID HUI ACW TRIFFITT PD CROZIER AEC GREGG PJ SINCLAIR ME ARMSTRONG AL MITCHELL VE
Citation: Id. Dunn et al., PLASMA D-DIMER AS A MARKER FOR POSTOPERATIVE DEEP VENOUS THROMBOSIS -A STUDY AFTER TOTAL HIP OR KNEE ARTHROPLASTY, Thrombosis and haemostasis, 72(5), 1994, pp. 663-665

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

Authors: GREEN PM MITCHELL VE MCGRAW A GOLDMAN E GIANNELLI F
Citation: Pm. Green et al., HEMOPHILIA-B CAUSED BY A MISSENSE MUTATION IN THE PREPEPTIDE SEQUENCEOF FACTOR-IX, Human mutation, 2(2), 1993, pp. 103-107

Authors: MURPHY P SIVAKUMARAN M PAVORD S PATEL R SHORT M HUTCHINSON RM MITCHELL VE
Citation: P. Murphy et al., UNIQUE PRESENTATION OF A CLONAL T-GAMMA-DELTA CELL LYMPHOPROLIFERATIVE DISORDER, POSSIBLE EVOLUTION FROM AN OLIGOCLONAL EXPANSION OF T-GAMMA-DELTA CELLS IN THE INTESTINAL EPITHELIUM OF A PATIENT WITH CELIAC-DISEASE, British Journal of Haematology, 84, 1993, pp. 40-40
Risultati: 1-11 |