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Results: 1-25/29
Authors:
RAHIMY MC
KRISHNAMOORTHY R
AHOUIGNAN G
LAFFAN M
VULLIAMY T
Citation: Mc. Rahimy et al., THE 20210A ALLELE OF PROTHROMBIN IS NOT FOUND AMONG SICKLE-CELL DISEASE PATIENTS FROM WEST-AFRICA, Thrombosis and haemostasis, 79(2), 1998, pp. 444-445
Authors:
AMROLIA PJ
KAEDA J
VULLIAMY T
ROPER D
DOKAL I
ROBERTS IAG
Citation: Pj. Amrolia et al., ANALYSIS OF CHIMERISM IN CHILDREN WITH HEMOGLOBINOPATHIES UNDERGOING STEM-CELL TRANSPLANTATION, British Journal of Haematology, 101, 1998, pp. 174-174
Authors:
MUMFORD AD
VULLIAMY T
LINDSAY J
WATSON A
Citation: Ad. Mumford et al., HEREDITARY HYPERFERRITINEMIA-CATARACT SYNDROME - 2 NOVEL MUTATIONS INTHE L-FERRITIN IRON-RESPONSIVE ELEMENT, Blood, 91(1), 1998, pp. 367-368
Authors:
VULLIAMY T
LUZZATTO L
HIRONO A
BEUTLER E
Citation: T. Vulliamy et al., HEMATOLOGICALLY IMPORTANT MUTATIONS - GLUCOSE-6-PHOSPHATE-DEHYDROGENASE, Blood cells, molecules, & diseases, 23(15), 1997, pp. 302-313
Authors:
SPENCER A
VULLIAMY T
KAEDA J
GOLDMAN JM
MELO JV
Citation: A. Spencer et al., CLONAL INSTABILITY PRECEDING LYMPHOID BLASTIC TRANSFORMATION OF CHRONIC MYELOID-LEUKEMIA, Leukemia, 11(2), 1997, pp. 195-201
Authors:
KNIGHT S
VULLIAMY T
DEVRIENDT K
MASON P
DOKAL I
Citation: S. Knight et al., FURTHER REFINEMENT OF THE LOCUS FOR DYSKERATOSIS-CONGENITA WITHIN XQ28, Journal of Medical Genetics, 34, 1997, pp. 1001-1001
Authors:
KNIGHT SW
VULLIAMY T
MASON PJ
DOKAL I
Citation: Sw. Knight et al., INITIAL ANALYSIS FROM THE DYSKERATOSIS-CONGENITA REGISTRY (DCR), Blood, 90(10), 1997, pp. 1958-1958
Authors:
MUMFORD AD
VULLIAMY T
WATSON A
Citation: Ad. Mumford et al., HEREDITARY HYPERFERRITINEMIA-CATARACT SYNDROME IN A FAMILY WITH A NOVEL -C-]A SUBSTITUTION IN THE UPPER STEM OF THE L-FERRITIN GENE IRON-RESPONSIVE ELEMENT(36), Blood, 90(10), 1997, pp. 2678-2678
Authors:
KNIGHT SW
VULLIAMY T
DEVRIENDT K
MASON PJ
DOKAL I
Citation: Sw. Knight et al., REFINEMENT OF THE CANDIDATE GENE REGION FOR X-LINKED DYSKERATOSIS-CONGENITA, American journal of human genetics, 61(4), 1997, pp. 1636-1636
Authors:
BEUTLER E
VULLIAMY T
LUZZATTO L
Citation: E. Beutler et al., HEMATOLOGICALLY IMPORTANT MUTATIONS - GLUCOSE-6-PHOSPHATE-DEHYDROGENASE, Blood cells, molecules, & diseases, 22(4), 1996, pp. 49-56
Authors:
VULLIAMY T
ROVIRA A
YUSOFF N
COLOMER D
LUZZATTO L
VIVESCORRONS JL
Citation: T. Vulliamy et al., INDEPENDENT ORIGIN OF SINGLE AND DOUBLE MUTATIONS IN THE HUMAN GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE, Human mutation, 8(4), 1996, pp. 311-318
Authors:
OROURKE N
KELLY S
VULLIAMY T
PRICE P
Citation: N. Orourke et al., PRIMARY KI-1 LYMPHOMA AND THE ETIOLOGY OF B-SYMPTOMS, European journal of cancer, 32A(5), 1996, pp. 902-903
Authors:
NAFA K
BESSLER M
MASON P
VULLIAMY T
HILLMEN P
CASTROMALASPINA H
LUZZATTO L
Citation: K. Nafa et al., FACTOR-V LEIDEN MUTATION INVESTIGATED BY AMPLIFICATION CREATED RESTRICTION ENZYME SITE (ACRES) IN PNH PATIENTS WITH AND WITHOUT THROMBOSIS, Haematologica, 81(6), 1996, pp. 540-542
Authors:
LAFFAN MA
VULLIAMY T
SCHMITZ E
SWIRSKY D
Citation: Ma. Laffan et al., FACTOR-V LEIDEN AND SICKLE-CELL DISEASE, Thrombosis and haemostasis, 75(5), 1996, pp. 859-860
Authors:
KNIGHT SW
VULLIAMY T
FORNI GL
OSCIER D
MASON PJ
DOKAL I
Citation: Sw. Knight et al., FINE MAPPING OF THE DYSKERATOSIS-CONGENITA LOCUS IN XQ28, Journal of Medical Genetics, 33(12), 1996, pp. 993-995
Authors:
KNIGHT SW
VULLIAMY T
MASON PJ
DOKAL I
Citation: Sw. Knight et al., MOLECULAR APPROACHES TO IDENTIFYING THE DYSKERATOSIS-CONGENITA GENE, British Journal of Haematology, 93, 1996, pp. 30-30
Authors:
KAEDA JS
RAY PF
BINGHAM J
VULLIAMY T
DOKAL I
ROBERTS IA
WINSTON RML
HANDYSIDE A
Citation: Js. Kaeda et al., PREIMPLANTATION GENETIC DIAGNOSIS OF BETA-THALASSEMIA MAJOR - ACCURATE DETECTION OF MUTATIONS FOLLOWING SINGLE-CELL AMPLIFICATION, British Journal of Haematology, 93, 1996, pp. 198-198
Authors:
KAEDA JS
KOTEA R
SHUN NK
MANRAJ M
KRISHNAMOORTHY R
BAUTISTA JM
VULLIAMY T
MASON PJ
LUZZATTO L
Citation: Js. Kaeda et al., G6PD DEFICIENCY ON THE ISLAND OF MAURITIUS, British Journal of Haematology, 93, 1996, pp. 326-326
Authors:
KNIGHT SW
VULLIAMY T
MASON PJ
Citation: Sw. Knight et al., FINE MAPPING OF THE DYSKERATOSIS-CONGENITA LOCUS WITHIN XQ28, Blood, 88(10), 1996, pp. 1222-1222
Authors:
SPENCER A
VULLIAMY T
CHASE A
GOLDMAN JM
Citation: A. Spencer et al., MYELOID TO LYMPHOID CLONAL SUCCESSION FOLLOWING AUTOLOGOUS TRANSPLANTATION IN 2ND CHRONIC PHASE OF CHRONIC MYELOID-LEUKEMIA, Leukemia, 9(12), 1995, pp. 2138-2139
Authors:
ROVIRA A
VULLIAMY T
PUJADES MA
LUZZATTO L
CORRONS JLV
Citation: A. Rovira et al., MOLECULAR-GENETICS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) DEFICIENCY IN SPAIN - IDENTIFICATION OF 2 NEW POINT MUTATIONS IN THE G6PD GENE, British Journal of Haematology, 91(1), 1995, pp. 66-71
Authors:
NAFA K
BESSLER M
HILLMEN P
MASON PJ
VULLIAMY T
CASTROMALASPINA H
LUZZATTO L
Citation: K. Nafa et al., FACTOR-V LEIDEN MUTATION INVESTIGATED BY A MODIFIED PCR TECHNIQUE IN PNH PATIENTS WITH THROMBOSIS, Blood, 86(10), 1995, pp. 807-807
Authors:
SPENCER A
VULLIAMY T
GOLDMAN JM
MELO JV
Citation: A. Spencer et al., IMMUNOGLOBULIN HEAVY-CHAIN GENE REARRANGEMENTS ASSOCIATED WITH LYMPHOID BLAST CRISIS OF CHRONIC MYELOID-LEUKEMIA EVIDENCE FOR CLONAL SUCCESSION IN THE B-LYMPHOID LINEAGE BEFORE THE ONSET OF BLASTIC TRANSFORMATION, Blood, 86(10), 1995, pp. 2090-2090
Authors:
NAFA K
REGHIS A
OSMANI N
BAGHLI L
AITABBES H
BENABADJI M
KAPLAN JC
VULLIAMY T
LUZZATTO L
Citation: K. Nafa et al., AT LEAST 5 POLYMORPHIC MUTANTS ACCOUNT FOR THE PREVALENCE OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY IN ALGERIA, Human genetics, 94(5), 1994, pp. 513-517
Authors:
KAEDA JS
PRASAD K
HOWARD RJ
MEHTA A
VULLIAMY T
LUZZATTO L
Citation: Js. Kaeda et al., MANAGEMENT OF PREGNANCY WHEN MATERNAL BLOOD HAS A VERY HIGH-LEVEL OF FETAL HEMOGLOBIN, British Journal of Haematology, 88(2), 1994, pp. 432-434