Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Yvonne Grandison"'
Autor:
Beryl E. Serjeant, Graham R. Serjeant, Minerva Thame, Marvin Thompson, Douglas R. Higgs, J.S. Morris, Karlene Mason, Yvonne Grandison
Publikováno v:
Clinical and laboratory haematology. 13(3)
The red cell distribution width (RDW) has been studied during the clinical steady state in 1121 patients with homozygous sickle cell (SS) disease, 344 with sickle cell-haemoglobin C (SC) disease, 68 with sickle cell-beta+ thalassaemia, 49 with sickle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e3250e84685f9302ea0b5cd1d2b8ec
http://ora.ox.ac.uk/objects/uuid:b7cf6c43-5166-483e-a226-3759d760c89f
http://ora.ox.ac.uk/objects/uuid:b7cf6c43-5166-483e-a226-3759d760c89f
Autor:
G.H. Maude, Yvonne Grandison, M. Beckford, Michael C. G. Stevens, Beryl E. Serjeant, B. Taylor, Graham R. Serjeant, Karlene Mason, J. M. Topley
Publikováno v:
British Journal of Haematology. 60:279-292
The haematological changes in early years following neonatal diagnosis have been observed in representative groups of children with sickle cell-haemoglobin C (SC) disease, sickle cell-beta(+) thalassaemia, and in sickle cell-beta(0) thalassaemia. Mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73bd365035fb5679699a46dd4eacc2de
https://doi.org/10.1111/j.1365-2141.1985.tb07414.x
https://doi.org/10.1111/j.1365-2141.1985.tb07414.x
Autor:
Annabelle Sewell, Yvonne Grandison, Graham R. Serjeant, Shubha Vaidya, Beryl E. Serjeant, Karlene Mason
Publikováno v:
Clinical & Laboratory Haematology. 2:169-178
Summary Haematological indices, including total haemoglobin, mean cell haemoglobin concentration, red cell count, mean cell volume, mean cell haemoglobin, reticulocytes, and serum iron values, in a cohort of 243 randomly selected Negro children with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::676be46f52b93c738331ffc02c476de4
https://doi.org/10.1111/j.1365-2257.1980.tb00821.x
https://doi.org/10.1111/j.1365-2257.1980.tb00821.x
Autor:
M. Beckford, H Teal, Beryl E. Serjeant, Yvonne Grandison, Michael C. G. Stevens, Karlene Mason, D J Weatherall, B. Taylor, G.H. Maude
Publikováno v:
Blood. 67:411-414
alpha Thalassemia modifies the hematologic expression of homozygous sickle cell (SS) disease, resulting in increased total hemoglobin and HbA2 and decreased HbF, mean cell volume, reticulocytes, irreversibly sickled cells, and bilirubin levels. The a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf78419285ec3e203bde0f3813dc0aac
https://doi.org/10.1182/blood.v67.2.411.411
https://doi.org/10.1182/blood.v67.2.411.411
Autor:
G R Serjeant, Karlene Mason, Yvonne Grandison, L. M. Rabb, Richard J. Hayes, Beryl E. Serjeant
Publikováno v:
Scopus-Elsevier
A double blind controlled trial of supplementation with folic acid has been performed in 117 children with homozygous sickle cell (SS) disease aged 6 months to 4 years over a 1 year period. No megaloblastic change was observed in either group. At the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::680c8ba3514b5b127b366c35c5df1e09
https://pubmed.ncbi.nlm.nih.gov/6347243
https://pubmed.ncbi.nlm.nih.gov/6347243
Autor:
Graham R. Serjeant, Yvonne Lowrie, Beryl E. Serjeant, Yvonne Grandison, Shuba Vaidya, Jennifer Phillips, Karlene Mason
Publikováno v:
British journal of haematology. 48(4)
A cohort study of sickle cell disease from birth has allowed observations on the disease without the symptomatic selection inherent in previous series. The development of haematological indices from birth to 6 years in male and female infants with ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95739c403c65f21b85fb1c10f842077a
https://pubmed.ncbi.nlm.nih.gov/7272216
https://pubmed.ncbi.nlm.nih.gov/7272216
Autor:
Beryl E. Serjeant, William G. Wood, Richard J. Hayes, Yvonne Grandison, Graham R. Serjeant, Karlene Mason, S. Vaidya And
Publikováno v:
British journal of haematology. 52(3)
The decline of fetal haemoglobin (Hb F) from birth to 6 years has been compared in a cohort of 266 Jamaican children with homozygous sickle cel (SS) disease and in 243 matched controls with a normal haemoglobin (AA) genotype. Hb F levels were signifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1049abb3ea38f24dd227e5c6cafd412a
https://pubmed.ncbi.nlm.nih.gov/6181802
https://pubmed.ncbi.nlm.nih.gov/6181802
Autor:
Yvonne Grandison, Yvonne Lowrie, Richard J. Hayes, Douglas R. Higgs, Beryl E. Serjeant, J. Lamb, Karlene Mason, Graham R. Serjeant, John B. Clegg, Beverley E. Aldridge, D. J. Weatherall
Publikováno v:
The New England journal of medicine. 306(24)
Patients with homozygous sickle-cell disease may be homozygous for alpha-thalassemia 2 (alpha-/alpha-), may be heterozygous for alpha-thalassemia 2 (alpha-/alpha alpha), or may have a normal alpha-globin-gene complement (alpha alpha/alpha alpha). We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96cc9b08abf65706b7fabb0ae8655ec9
https://pubmed.ncbi.nlm.nih.gov/6176865
https://pubmed.ncbi.nlm.nih.gov/6176865
Autor:
B. Taylor, Karlene Mason, Graham R. Serjeant, Douglas R. Higgs, Yvonne Grandison, Beryl E. Serjeant, G.H. Maude, M. Beckford
Publikováno v:
Clinical and laboratory haematology. 7(4)
Haematological indices were studied from birth to 9 years in a representative sample of 195 children with a normal haemoglobin (AA) genotype subdivided according to the number of alpha globin genes. These were 5 homozygotes for alpha-thalassaemia 2 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8cc6fb623f7af8938b61c7b47849232
https://pubmed.ncbi.nlm.nih.gov/2420505
https://pubmed.ncbi.nlm.nih.gov/2420505
Autor:
G R Serjeant, M. Beckford, Beryl E. Serjeant, Richard J. Hayes, Karlene Mason, Yvonne Grandison
Publikováno v:
Scopus-Elsevier
Summary The steady state haematological characteristics observed in 1071 patients with homozygous sickle cell (SS) disease aged 5–66 years are presented. Cross sectional studies indicated that HbA2 levels were consistently higher in males but no ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8168ac41fd31d13d1a7626ac6eceb0d9
http://www.scopus.com/inward/record.url?eid=2-s2.0-0021911330&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0021911330&partnerID=MN8TOARS
