Search Results - "Keidan, A. J."

Guidelines for the diagnosis and management of acquired aplastic anaemia by Marsh, J.C.W., Ball, S.E., Darbyshire, P., Gordon‐Smith, E.C., Keidan, A.J., Martin, A., McCann, S.R., Mercieca, J., Oscier, D., Roques, A.W.W., Yin, J.A.L.

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Routine antenatal anti-D prophylaxis by Keidan, A. J.

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Polymerization of sickle cell hemoglobin at arterial oxygen saturation impairs erythrocyte deformability by GREEN, M. A, NOGUCHI, C. T, KEIDAN, A. J, MARWAH, S. S, STUART, J

“…We have examined the filterability of sickle erythrocytes, using an initial-flow-rate method, to determine whether sufficient hemoglobin S polymer forms at…”
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Delayed haemolytic transfusion reaction due to anti‐Jkb in a patient with non‐Hodgkin’s lymphoma‐transient nature of anti‐Jkb and the importance of early serological diagnosis by Hussain, S. S., Ebbs, A. M., Curtin, N. J., Keidan, A. J.

“…summary Delayed haemolytic transfusion reactions (DHTRs) are relatively common following blood transfusions. In the UK, DHTRs were responsible for 10.2% of all…”
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Rheological effects of bed rest in sickle cell disease by Keidan, A J, Stuart, J

“…A serial rheological study in two patients with homozygous sickle cell disease whose leg ulcers healed as a consequence of bed rest showed an improvement in…”
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Erythrocyte heterogeneity in sickle cell disease: effect of deoxygenation on intracellular polymer formation and rheology of sub-populations by Keidan, A J, Noguchi, C T, Player, M, Chalder, S M, Stuart, J

“…Erythrocytes from 12 patients with homozygous sickle cell disease in the steady state were fractionated on a Percoll-Stractan density gradient. Erythrocyte…”
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Pharmacological modification of oxygen affinity improves deformability of deoxygenated sickle erythrocytes: a possible therapeutic approach to sickle cell disease by Keidan, A J, Sowter, M C, Johnson, C S, Marwah, S S, Stuart, J

“…1. The formation of polymerized haemoglobin S in sickle cells is critically dependent on the concentration of deoxygenated haemoglobin so that compounds which…”
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Recurrence of neutropenia associated with splenunculus by Keidan, A J, Bareford, D

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Infective complications of aplastic anaemia by Keidan, A J, Tsatalas, C, Cohen, J, Cousins, S, Gordon-Smith, E C

“…Patients with aplastic anaemia have a relatively specific immune defect--leucopenia with neutropenia. We have carried out a retrospective analysis of infective…”
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Painful sickle cell crises precipitated by stopping prophylactic exchange transfusions by Keidan, A J, Marwah, S S, Vaughan, G R, Franklin, I M, Stuart, J

“…A patient with homozygous sickle cell disease showed a reduced incidence of painful crises as a result of regular exchange transfusion, but on three occasions…”
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Oxpentifylline and cetiedil citrate improve deformability of dehydrated sickle cells by Stuart, J, Stone, P C, Bilto, Y Y, Keidan, A J

“…Erythrocytes from 14 patients with homozygous sickle cell anaemia were treated with the calcium ionophore A23187 to induce loss of cellular potassium and…”
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Transfusion-Associated HIV Infection by Keidan, A J

“…To the Editor: In their article on the natural history of transfusion-associated infection with HIV, Ward et al. (Oct. 5 issue)* found that the majority of…”
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Effect of polymerization tendency on haematological, rheological and clinical parameters in sickle cell anaemia by Keidan, A J, Sowter, M C, Johnson, C S, Noguchi, C T, Girling, A J, Stevens, S M, Stuart, J

“…The polymerization tendency of sickle haemoglobin was estimated as a function of oxygen saturation in 30 patients with homozygous sickle cell anaemia. The…”
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Unexplained lymphadenopathy in sickle cell disease by Keidan, A J, Hamon, M D, Franklin, I M, Mawson, S

“…Progressive lymphadenopathy in a previously healthy female adult with homozygous sickle cell disease (SCD) was found to be due to infection with the human…”
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Laboratory tests for monitoring prophylactic exchange transfusion in pregnancy complicated by sickle cell disease by Keidan, A J, Marwah, S S, Bareford, D, Franklin, I M, Stuart, J

“…Prophylactic exchange transfusion is of uncertain value in pregnancy complicated by sickle cell disease (SCD), and there is a lack of laboratory tests to…”
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Uncommon complications of hairy cell leukaemia by Keidan, A J, Liu Yin, J A, Gordon-Smith, E C

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Hypereosinophilic syndrome preceding T cell lymphoblastic lymphoma by Keidan, A J, Catovsky, D, Tavares de Castro, J, Spry, C J

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AML autografting--is there a need for CNS prophylaxis? by Keidan, A J, Jan-Mohamed, R, Leyland, M J, Franklin, I M

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Testing for HIV: the non-medicolegal view by Keidan, A J, Franklin, I M, Pinching, A J

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Effect of BW12C on oxygen affinity of haemoglobin in sickle-cell disease by Keidan, A J, Franklin, I M, White, R D, Joy, M, Huehns, E R, Stuart, J

“…Eight subjects with sickle-cell disease in the symptom-free steady-state received a single one-hour infusion of the new anti-sickling agent BW12C on a total of…”
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