Search Results - "Bareford, D"

A survey on patient perception of reduced-intensity transplantation in adults with sickle cell disease by CHAKRABARTI, S, BAREFORD, D

“…The development of reduced-intensity conditioning (RIC) and the success of BMT for paediatric sickle cell disease (SCD) have raised the possibility of…”
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Priapism in sickle‐cell disease; incidence, risk factors and complications – an international multicentre study by Adeyoju, A.B., Olujohungbe, A.B.K., Morris, J., Yardumian, A., Bareford, D., Akenova, A., Akinyanju, O., Cinkotai, K., O'Reilly, P.H.

“…Objective  To define the incidence, risk factors and complications of priapism in a large population of patients with sickle‐cell anaemia in five centres in…”
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Guidelines for the diagnosis, investigation and management of polycythaemia/erythrocytosis by MCMULLIN, Mary F, BAREFORD, D, RYAN, Kate, PEARSON, T. C, WILKINS, Bridget, CAMPBELL, P, GREEN, A. R, HARRISON, Claire, HUNT, Beverley, OSCIER, D, POLKEY, M. I, REILLY, J. T, ROSENTHAL, E

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Methylation of the suppressor of cytokine signaling 3 gene (SOCS3) in myeloproliferative disorders by Fourouclas, Nasios, Li, Juan, Gilby, Daniel C, Campbell, Peter J, Beer, Philip A, Boyd, Elaine M, Goodeve, Anne C, Bareford, David, Harrison, Claire N, Reilly, John T, Green, Anthony R, Bench, Anthony J

“…1 University of Cambridge, Department of Haematology, Cambridge Institute for Medical Research, Cambridge 2 Academic Unit of Haematology, School of Medicine…”
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Best practice in primary care pathology: review 1 by Smellie, W S A, Wilson, D, McNulty, C A M, Galloway, M J, Spickett, G A, Finnigan, D I, Bareford, D A, Greig, M A, Richards, J

“…This first best practice review examines four series of common primary care questions in laboratory medicine, namely: (i) measurement and monitoring of…”
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Day case management of sickle pain: 3 years experience in a UK sickle cell unit by Wright, J., Bareford, D., Wright, C., Augustine, G., Olley, K., Musamadi, L, Dhanda, C., Knight, C.

“…Summary A day centre was established to determine whether an alternative approach to the management of uncomplicated sickle pain would improve the quality of…”
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THE LABORATORY DIAGNOSIS OF HAEMOGLOBINOPATHIES by Bain, B J, Amos, R J, Bareford, D, Chapman, C

“…The laboratory diagnosis of haemoglobinopathies, including the thalassaemias, is of growing importance, particularly because of an increasing requirement for…”
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Interferon α and zidovudine therapy in adult T‐cell leukaemia lymphoma: response and outcome in 15 patients by Matutes, E., Taylor, G. P., Cavenagh, J., Pagliuca, A., Bareford, D., Domingo, A., Hamblin, M., Kelsey, S., Mir, N., Reilly, J. T.

“…Adult T‐cell leukaemia lymphoma (ATLL) is an aggressive disease caused by the human T‐lymphotropic virus 1 (HTLV‐I) with a short survival. Responses to…”
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Best practice in primary care pathology: review 3 by Smellie, W S A, Forth, J, Bareford, D, Twomey, P, Galloway, M J, Logan, E C M, Smart, S R S, Reynolds, T M, Waine, C

“…This best practice review examines four series of common primary care questions in laboratory medicine: (i) “minor” blood platelet count and haemoglobin…”
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Soluble P-selectin and vascular endothelial growth factor in steady state sickle cell disease: relationship to genotype by Blann, A. D., Mohan, J. S., Bareford, D., Lip, G. Y. H.

“…Sickle cell disease (SCD) is characterised by abnormal coagulopathy and angiogenesis although their relationships in two common genotypes, homozygous (HbSS)…”
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Ethnic background is a determinant of average warfarin dose required to maintain the INR between 3.0 and 4.5 by Blann, A., Bareford, D.

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Remission induction in a Jehovah's Witness patient with acute myeloid leukaemia using gemtuzumab ozogamicin by Bareford, D., Odeh, B., Narayanan, S., Wiltshire, S.

“…A 40‐year‐old patient, who was a Jehovah's Witness, with acute myeloid leukaemia entered remission using a chemotherapeutic based regime aided by the addition…”
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The angiopoietin/Tie-2 system in proliferative sickle retinopathy: relation to vascular endothelial growth factor, its soluble receptor Flt-1 and von Willebrand factor, and to the effects of laser treatment by Mohan, J S, Lip, P L, Blann, A D, Bareford, D, Lip, G Y H

“…Aim: To determine plasma levels of angiopoietin-1 and angiopoietin-2 (Ang-1, Ang-2), their soluble receptor Tie-2, vascular endothelial growth factor (VEGF),…”
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Increased soluble P-selectin in patients with haematological and breast cancer: a comparison with fibrinogen, plasminogen activator inhibitor and von Willebrand factor by Blann, A D, Gurney, D, Wadley, M, Bareford, D, Stonelake, P, Lip, G Y. H

“…Abnormal platelet activation and an increased risk of thrombosis are frequent findings in cancer. As soluble adhesion molecule P-selectin is being increasingly…”
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Best practice in primary care pathology: review 7 by Smellie, W S A, Forth, J, Smart, S R S, Galloway, M J, Irving, W, Bareford, D, Collinson, P O, Kerr, K G, Summerfield, G, Carey, P J, Minhas, Rubin

“…This seventh best-practice review examines four series of common primary care questions in laboratory medicine: (1) blood count abnormalities 2; (2) cardiac…”
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Best practice in primary care pathology: review 2 by Smellie, W S, Forth, J O, McNulty, C A M, Hirschowitz, L, Lilic, D, Gosling, R, Bareford, D, Logan, E, Kerr, K G, Spickett, G P, Hoffman, J, Galloway, A, Bloxham, C A

“…This second best practice review examines five series of common primary care questions in laboratory medicine: (1) laboratory testing for allergy, (2)…”
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Blood lead levels in iron-deficient and noniron-deficient adults by ALABDULLAH, H., BAREFORD, D., BRAITHWAITE, R., CHIPMAN, K.

“…Summary Iron deficiency (ID) has been reported to increase lead absorption. This relationship has been investigated in detail in children but not in adults…”
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Platelet P-selectin and platelet mass, volume and component in sickle cell disease: Relationship to genotype by Mohan, J.S., Lip, G.Y.H., Bareford, D., Blann, A.D.

“…Excess platelet activation (e.g. increased soluble P selectin [sPsel] and beta thromboglobulin [β-TG]) is well established in sickle cell disease (SCD) and may…”
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Angiotropic large cell lymphoma presenting as intestinal obstruction by Quadri, A. M., Sylvester, S., Verma, S., Bareford, D., Spychal, R. T., Jones, E. L., Ganesan, R.

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Splenic rupture as a consequence of dual malignant pathology: a case report by Hoar, F J, Chan, S-Y, Stonelake, P S, Wolverson, R W, Bareford, D

“…A 76 year old woman presented acutely with non-traumatic splenic rupture, which was successfully treated by emergency splenectomy. Histological examination of…”
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