Search Results - "KAEDA, J. S"

A new glucose-6-phosphate dehydrogenase variant, G6PD Orissa (44 Ala→Gly), is the major polymorphic variant in tribal populations in India by KAEDA, J. S, CHHOTRAY, G. P, MASON, P. J, RANJIT, M. R, BAUTISTA, J. M, REDDY, P. H, STEVENS, D, NAIDU, J. M, BRITT, R. P, VULLIAMY, T. J, LUZZATTO, L

“…Deficiency of glucose-6-phosphate dehydrogenase (G6PD) is usually found at high frequencies in areas of the world where malaria has been endemic. The frequency…”
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Three major G6PD‐deficient polymorphic variants identified among the Mauritian population by Kotea, R., Kaeda, J. S., Yan, S. L. K., Sem Fa, N., Beesoon, S., Jankee, S., Ramasawmy, R., Vulliamy, T., Bradnock, R. W., Bautista, J., Luzzatto, L., Krishnamoorthy, R., Mason, P. J.

“…We report the results of the first epidemiological study investigating glucose 6‐phosphate dehydrogenase (G6PD) deficiency among the heterogenous Mauritian…”
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Clinical Decision Making in Chronic Myeloid Leukemia Based on Polymerase Chain Reaction Analysis of Minimal Residual Disease by Goldman, John M., Kaeda, Jaspal S., Cross, Nicholas C.P., Hochhaus, Andreas, Hehlmann, Rüdiger

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Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia by Vulliamy, Tom J., Kaeda, Jaspal S., Ait‐Chafa, Dahlila, Mangerini, Rosa, Roper, David, Barbot, Jose, Mehta, Athul B., Athanassiou‐Metaxa, Luzzatto, Lucio, Mason, Philip J.

“…We have determined the causative mutation in 12 cases of glucose‐6‐phosphate dehydrogenase deficiency associated with chronic non‐spherocytic haemolytic…”
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New Glucose-6-Phosphate Dehydrogenase Mutations Associated With Chronic Anemia by Mason, P.J., Sonati, M.F., MacDonald, D., Lanza, C., Busutil, D., Town, M., Corcoran, CM, Kaeda, J.S., Stevens, D.J., Al-lsmail, S., Altay, C., Hatton, C., Lewis, D.S., McMullin, M.F., Meloni, T., Paul, B., Pippard, M., Prentice, A.G., Vulliamy, T.J., Luzzatto, L.

“…We have identified the glucose-6-phosphate dehydrogenase mutations responsible for enzyme deficiency in nine individuals with chronic nonspherocytic hemolytic…”
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Preimplantation genetic diagnosis of beta-thalassaemia major by Ray, P F, Kaeda, J S, Bingham, J, Roberts, I, Handyside, A H

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Severe hemolytic anemia associated with the homozygous state for an unstable hemoglobin variant (Hb Bushwick) by SRIVASTAVA, P, KAEDA, J. S, ROPER, D, VULLIAMY, T. J, BUCKLEY, M, LUZZATTO, L

“…We have investigated a 13-year-old girl from first cousin parents who presented with severe hemolytic anemia. Hematologic studies showed unstable hemoglobin…”
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Management of pregnancy when maternal blood has a very high level of fetal haemoglobin by Kaeda, J S, Prasad, K, Howard, R J, Mehta, A, Vulliamy, T, Luzzatto, L

“…Fetal blood normally has a higher oxygen affinity than maternal blood because of the predominance of haemoglobin (Hb) F in the former and of Hb A in the…”
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How and why minimal residual disease studies are necessary in leukemia: a review from WP10 and WP12 of the European LeukaemiaNet by Bene, Marie C, Kaeda, Jaspal S

“…1 Immunologie, CHU & Nancy Université, France 2 Departamento de Hematologia, Centro Hospitalar de Coimbra, Portugal Correspondence: Marie Christine Béné,…”
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Phase I/II trial of adding semisynthetic homoharringtonine in chronic myeloid leukemia patients who have achieved partial or complete cytogenetic response on imatinib by Marin, David, Kaeda, Jaspal S., Andreasson, Catharina, Saunders, Sue M., Bua, Marco, Olavarria, Eduardo, Goldman, John M., Apperley, Jane F.

“…BACKGROUND A Phase I/II study was designed to show whether the addition of semisynthetic homoharringtonine (sHHT) would reduce the level of residual disease in…”
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