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Results: 76-100/106
MANAGEMENT OF PREGNANCY WHEN MATERNAL BLOOD HAS A VERY HIGH-LEVEL OF FETAL HEMOGLOBIN
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
MUTATIONS IN THE PIG-A GENE CAUSING PARTIAL DEFICIENCY OF GPI-LINKED SURFACE-PROTEINS (PNH-II) IN PATIENTS WITH PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
Authors: BESSLER M MASON PJ HILLMEN P LUZZATTO L
Citation: M. Bessler et al., MUTATIONS IN THE PIG-A GENE CAUSING PARTIAL DEFICIENCY OF GPI-LINKED SURFACE-PROTEINS (PNH-II) IN PATIENTS WITH PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA, British Journal of Haematology, 87(4), 1994, pp. 863-866
MYELODYSPLASIA IN A PATIENT WITH PREEXISTING PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - A CLONAL DISEASE ORIGINATING FROM WITHIN A CLONAL DISEASE
Authors: LONGO L BESSLER M BERIS P SWIRSKY D LUZZATTO L
Citation: L. Longo et al., MYELODYSPLASIA IN A PATIENT WITH PREEXISTING PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - A CLONAL DISEASE ORIGINATING FROM WITHIN A CLONAL DISEASE, British Journal of Haematology, 87(2), 1994, pp. 401-403
GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY AND RED-CELL MEMBRANE DEFECTS - ADDITIVE OR SYNERGISTIC INTERACTION IN PRODUCING CHRONIC HEMOLYTIC-ANEMIA
Authors: ALFINITO F CALABRO LV CAPPELLINI ZMD FIORELLI G FILOSA S IOLASCON A DELGIUDICE EM PERROTTA S MIGLIORATI R VALLONE D ROTOLI B LUZZATTO L
Citation: F. Alfinito et al., GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY AND RED-CELL MEMBRANE DEFECTS - ADDITIVE OR SYNERGISTIC INTERACTION IN PRODUCING CHRONIC HEMOLYTIC-ANEMIA, British Journal of Haematology, 87(1), 1994, pp. 148-152
THE 3-DIMENSIONAL STRUCTURE OF G6PD HELPS TO EXPLAIN G6PD DEFICIENCY
Authors: MASON PI VULLIAMY TI BAUTISTA IM LUZZATTO L NAYLOR C ADAMS M
Citation: Pi. Mason et al., THE 3-DIMENSIONAL STRUCTURE OF G6PD HELPS TO EXPLAIN G6PD DEFICIENCY, Blood, 84(10), 1994, pp. 10000014-10000014
MUTATIONS IN THE PIG-A GENE CAUSING PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA (PNH) ARE MAINLY OF THE FRAMESHIFT TYPE
Authors: NAFA K MASON PJ HILLMEN P LUZZATTO L BESSLER M
Citation: K. Nafa et al., MUTATIONS IN THE PIG-A GENE CAUSING PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA (PNH) ARE MAINLY OF THE FRAMESHIFT TYPE, Blood, 84(10), 1994, pp. 10000216-10000216
TARGETED DISRUPTION OF THE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE IN MOUSE EMBRYONIC STEM-CELLS BY HOMOLOGOUS RECOMBINATION
Authors: PANDOLFI PP SONATI F RIVI R GROSVELD F LUZZATTO L
Citation: Pp. Pandolfi et al., TARGETED DISRUPTION OF THE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE GENE IN MOUSE EMBRYONIC STEM-CELLS BY HOMOLOGOUS RECOMBINATION, Blood, 84(10), 1994, pp. 10000504-10000504
MOLECULAR HETEROGENEITY OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) IN SPAIN AND IDENTIFICATION OF 2 NEW BASE SUBSTITUTIONS IN THE G6PD GENE
Authors: CORRONS JLV ROVIRA A PUJADES A VULLIAMY T LUZZATTO L
Citation: Jlv. Corrons et al., MOLECULAR HETEROGENEITY OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE (G6PD) IN SPAIN AND IDENTIFICATION OF 2 NEW BASE SUBSTITUTIONS IN THE G6PD GENE, Blood, 84(10), 1994, pp. 10000551-10000551
SIMILAR PATTERNS OF VK GENE USAGE BUT DIFFERENT DEGREES OF SOMATIC MUTATION IN HAIRY-CELL LEUKEMIA, PROLYMPHOCYTIC LEUKEMIA, WALDENSTROMS MACROGLOBULINEMIA, AND MYELOMA
Authors: WAGNER SD MARTINELLI V LUZZATTO L
Citation: Sd. Wagner et al., SIMILAR PATTERNS OF VK GENE USAGE BUT DIFFERENT DEGREES OF SOMATIC MUTATION IN HAIRY-CELL LEUKEMIA, PROLYMPHOCYTIC LEUKEMIA, WALDENSTROMS MACROGLOBULINEMIA, AND MYELOMA, Blood, 83(12), 1994, pp. 3647-3653
VARIANTS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE ARE DUE TO MISSENSE MUTATIONS SPREAD THROUGHOUT THE CODING REGION OF THE GENE
Authors: VULLIAMY T BEUTLER E LUZZATTO L
Citation: T. Vulliamy et al., VARIANTS OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE ARE DUE TO MISSENSE MUTATIONS SPREAD THROUGHOUT THE CODING REGION OF THE GENE, Human mutation, 2(3), 1993, pp. 159-167
LEUKEMIA - A GENETIC DISORDER OF HEMATOPOIETIC-CELLS
Authors: LUZZATTO L PANDOLFI PP
Citation: L. Luzzatto et Pp. Pandolfi, LEUKEMIA - A GENETIC DISORDER OF HEMATOPOIETIC-CELLS, BMJ. British medical journal, 307(6904), 1993, pp. 579-580
G6PD HAPLOTYPES SPANNING XQ28 FROM F8C TO RED-GREEN COLOR-VISION
Authors: FILOSA S CALABRO V LANIA G VULLIAMY TJ BRANCATI C TAGARELLI A LUZZATTO L MARTINI G
Citation: S. Filosa et al., G6PD HAPLOTYPES SPANNING XQ28 FROM F8C TO RED-GREEN COLOR-VISION, Genomics, 17(1), 1993, pp. 6-14
PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - CORRECTION OF ABNORMAL PHENOTYPE BY SOMATIC-CELL HYBRIDIZATION
Authors: HILLMEN P BESSLER M BUNGEY J LUZZATTO L
Citation: P. Hillmen et al., PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - CORRECTION OF ABNORMAL PHENOTYPE BY SOMATIC-CELL HYBRIDIZATION, Somatic cell and molecular genetics, 19(2), 1993, pp. 123-129
G6PD MEDITERRANEAN ACCOUNTS FOR THE HIGH PREVALENCE OF G6PD DEFICIENCY IN KURDISH JEWS
Authors: OPPENHEIM A JURY CL RUND D VULLIAMY TJ LUZZATTO L
Citation: A. Oppenheim et al., G6PD MEDITERRANEAN ACCOUNTS FOR THE HIGH PREVALENCE OF G6PD DEFICIENCY IN KURDISH JEWS, Human genetics, 91(3), 1993, pp. 293-294
SPECIFIC DEFECT IN N-ACETYLGLUCOSAMINE INCORPORATION IN THE BIOSYNTHESIS OF THE GLYCOSYLPHOSPHATIDYLINOSITOL ANCHOR IN CLONED CELL-LINES FROM PATIENTS WITH PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
Authors: HILLMEN P BESSLER M MASON PJ WATKINS WM LUZZATTO L
Citation: P. Hillmen et al., SPECIFIC DEFECT IN N-ACETYLGLUCOSAMINE INCORPORATION IN THE BIOSYNTHESIS OF THE GLYCOSYLPHOSPHATIDYLINOSITOL ANCHOR IN CLONED CELL-LINES FROM PATIENTS WITH PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA, Proceedings of the National Academy of Sciences of the United Statesof America, 90(11), 1993, pp. 5272-5276
DYSKERATOSIS-CONGENITA - 3 ADDITIONAL FAMILIES SHOW LINKAGE TO A LOCUS IN XQ28
Authors: ARNGRIMSSON R DOKAL I LUZZATTO L CONNOR JM
Citation: R. Arngrimsson et al., DYSKERATOSIS-CONGENITA - 3 ADDITIONAL FAMILIES SHOW LINKAGE TO A LOCUS IN XQ28, Journal of Medical Genetics, 30(7), 1993, pp. 618-619
EXPRESSION OF THE HUMAN G6PD GENE IN TRANSFECTED CELLS AND TRANSGENICMICE
Authors: CORCORAN C FRASER P LIDA J MARTINI G LUZZATTO L MASON PJ
Citation: C. Corcoran et al., EXPRESSION OF THE HUMAN G6PD GENE IN TRANSFECTED CELLS AND TRANSGENICMICE, British Journal of Haematology, 84, 1993, pp. 5-5
SEARCH FOR THE MOLECULAR LESION OF PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
Authors: BESSLER M MASON PJ HILLMEN P LUZZATTO L
Citation: M. Bessler et al., SEARCH FOR THE MOLECULAR LESION OF PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA, British Journal of Haematology, 84, 1993, pp. 7-7
SOMATIC MUTATION IN B-CELL LEUKEMIAS
Authors: WAGNER SD MARTINELLI V LUZZATTO L
Citation: Sd. Wagner et al., SOMATIC MUTATION IN B-CELL LEUKEMIAS, British Journal of Haematology, 84, 1993, pp. 13-13
GENETIC-HETEROGENEITY OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCYREVEALED BY SINGLE-STRAND CONFORMATION AND SEQUENCE-ANALYSIS
Authors: MASON PJ CALABRO V FILOSA S CIVITELLI D CITTADELLA R TAGARELLI A MARTINI G BRANCATI C LUZZATTO L
Citation: Pj. Mason et al., GENETIC-HETEROGENEITY OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCYREVEALED BY SINGLE-STRAND CONFORMATION AND SEQUENCE-ANALYSIS, British Journal of Haematology, 84, 1993, pp. 23-23
MYELODYSPLASIA IN A PATIENT WITH PREEXISTING PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - A CLONAL DISEASE WITHIN A CLONAL DISEASE
Authors: LONGO L BESSLER M BERIS P SWIRSKY D LUZZATTO L
Citation: L. Longo et al., MYELODYSPLASIA IN A PATIENT WITH PREEXISTING PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA - A CLONAL DISEASE WITHIN A CLONAL DISEASE, British Journal of Haematology, 84, 1993, pp. 34-34
APOPTOSIS IN MYELOMA
Authors: WAGNER SD BIRD J SAMSON D LUZZATTO L
Citation: Sd. Wagner et al., APOPTOSIS IN MYELOMA, British Journal of Haematology, 84, 1993, pp. 42-42
G6PD DEFICIENCY IN VANUATU, SW PACIFIC
Authors: GANCZAKOWSKI M TOWN M KANEKO A BOWDEN DK CLEGG JB WEATHERALL DJ LUZZATTO L
Citation: M. Ganczakowski et al., G6PD DEFICIENCY IN VANUATU, SW PACIFIC, British Journal of Haematology, 84, 1993, pp. 62-62
THE IDENTIFICATION OF THE BIOCHEMICAL DEFECT IN CELL-LINES FROM 9 PATIENTS WITH PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
Authors: HILLMEN P BESSLER M MASON PJ WATKINS WM LUZZATTO L
Citation: P. Hillmen et al., THE IDENTIFICATION OF THE BIOCHEMICAL DEFECT IN CELL-LINES FROM 9 PATIENTS WITH PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA, British Journal of Haematology, 84, 1993, pp. 62-62
SERUM ERYTHROPOIETIN LEVELS IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
Authors: MCMULLIN MF ELDER E HILLMEN P LUZZATTO L
Citation: Mf. Mcmullin et al., SERUM ERYTHROPOIETIN LEVELS IN PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA, British Journal of Haematology, 84, 1993, pp. 62-62
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