R. Amos

发表

Comparison of serial serum ferritin measurements and liver iron concentration assessed by MRI in adult transfused patients with sickle cell disease

R. Nzouakou, V. Ameen, D. Tsitsikas, 2014, European journal of haematology.

INCIDENCE AND PATHOGENESIS OF ACUTE MEGALOBLASTIC BONE-MARROW CHANGE IN PATIENTS RECEIVING INTENSIVE CARE

D. Mollin, C. Hinds, J. Amess, 1982, The Lancet.

Clinical outcomes in children with sickle cell disease living in England: a neonatal cohort in East London.

F. Kirkham, O. Wilkey, S. Chakravorty, 2007, Haematologica.

Observations on the haemopoietic response to critical illness.

C. Hinds, M. Deane, J. Amess, 1990, Journal of clinical pathology.

Regular automated red cell exchange transfusion in the management of pulmonary hypertension in sickle cell disease

R. Nzouakou, H. Seligman, D. Tsitsikas, 2014, British journal of haematology.

Safety, tolerability, and outcomes of regular automated red cell exchange transfusion in the management of sickle cell disease

R. Nzouakou, D. Tsitsikas, B. Sirigireddy, 2016, Journal of clinical apheresis.

Prevention of nitrous oxide-induced megaloblastic changes in bone marrow using folinic acid.

G. Rees, J. Amess, D. Nancekievill, 1984, British journal of anaesthesia.

Bone Marrow Hypoplasia During Intensive Care: Bone Marrow Culture Studies Implicating Ranitidine in the Suppression of Haemopoiesis

C. Hinds, J. Amess, J. Amess, 1987, Human toxicology.

Nucleoside incorporation into DNA and RNA in acute leukaemia: differences between the various leukaemia sub‐types

A. Piga, K. Ganeshaguru, H. Prentice, 1982, British journal of haematology.

Automated Red Cell Exchange in the Management of Sickle Cell Disease

M. Sharma, D. Tsitsikas, R. Amos, 2021, Journal of clinical medicine.

Successful outcome of three patients with sickle‐cell disease and fat embolism syndrome treated with intensive exchange transfusion

V. Mathew, C. Peters, S. Rowe, 2016, Clinical case reports.

Bone marrow necrosis and fat embolism syndrome in sickle cell disease: increased susceptibility of patients with non-SS genotypes and a possible association with human parvovirus B19 infection.

G. Gallinella, P. Greaves, H. Seligman, 2014, Blood reviews.

Toxicity of bone marrow in dentists exposed to nitrous oxide.

R. Bingham, B. Sweeney, P. Cole, 1985, British medical journal.

Autosomal inheritance of sideroblastic anaemia.

A. Miller, J. Amess, R. Amos, 1988, Clinical and laboratory haematology.

Guidelines for the enumeration of CD4+ T lymphocytes in immunosuppressed individuals. CD4+ T lymphocyte Working Party. Members of the General Haematology Task Force of BCSH.

B. Bain, K. Hyde, J. England, 1997, Clinical and laboratory haematology.

Guidelines on the investigation and diagnosis of cobalamin and folate deficiencies. A publication of the British Committee for Standards in Haematology. BCSH General Haematology Test Force.

J. Linnell, R. Leeming, R. Amos, 2008, Clinical and laboratory haematology.

The effect of histamine H2 receptor antagonists on platelet aggregation in man.

M. Horton, R. Jones, R. Amos, 2009, Scandinavian journal of haematology.

Investigations into the effect of nitrous oxide anaesthesia on folate metabolism in patients receiving intensive care.

D. Mollin, C. Hinds, J. Amess, 1985, Chemioterapia : international journal of the Mediterranean Society of Chemotherapy.

Cytosine arabinoside in the management of recurrent leukaemia

T. Lister, M. Barnett, A. Man, 1987, Hematological oncology.

Regular automated red cell exchange transfusion in the management of stuttering priapism complicating sickle cell disease

A. Ekong, D. Tsitsikas, R. Amos, 2018, British Journal of Haematology.

Distinct patterns of response to transfusion therapy for different chronic complications of sickle cell disease: A useful insight.

A. Agapidou, D. Tsitsikas, R. Amos, 2017, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

AZATHIOPRINE AND SEVERE BONE MARROW DEPRESSION

R. Thomas, J. Maddocks, L. Lennard, 1986, The Lancet.

Factors Affecting Hospital Staff Judgments About Sickle Cell Disease Pain

J. Elander, M. Marczewska, Sekayi Tangayi, 2006, Journal of Behavioral Medicine.

Role of S-adenosylmethionine in DNA synthesis and haemopoiesis.

J. Amess, R. Amos, N. Sourial, 2009, Scandinavian Journal of Haematology.

Hb Bart's in Cord Blood: An Accurate Indicator of α-Thalassemia

C. Fisher, J. Old, A. Stephens, 2006, Hemoglobin.

The laboratory diagnosis of malaria

B. Bain, K. Hyde, P. Chiodini, 1997 .

A 5-year cost analysis of automated red cell exchange transfusion for the management of recurrent painful crises in adult patients with sickle cell disease.

A. Ekong, B. Solanki, D. Tsitsikas, 2017, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.