Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Laura Steedman"'
Autor:
Sahar Mansour, C. McMahon, Nicholas Parkin, A. Mijovic, A. Bybee, M. Layton, M. Manansala, David C. Rees, Subarna Chakravorty, C. Laas, Laura Steedman, R. Mayhew, E. Moldes Beiro, Barnaby Clark, C. Lambert, Frances Smith
Publikováno v:
HemaSphere. 3:406-407
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8226fd9ad100d85291dc9feaf829041
https://doi.org/10.1097/01.hs9.0000561884.03682.dd
https://doi.org/10.1097/01.hs9.0000561884.03682.dd
Autor:
Eva Moldes Beiro, Barnaby Clark, Laura Steedman, Judith C. W. Marsh, Shreyans Ghandi, Peter Rushton, Frances Smith, Rachel Mayhew, Nicholas Parkin, Ghulam J. Mufti, Alison Bybee, Antonio Pagliuca, Austin G. Kulasekararaj, David C. Rees, David Brawand, Sahar Mansour, Subarna Chakravorty
Publikováno v:
Blood. 132:3609-3609
The genetic diagnosis of inherited anaemias is an important aspect of the diagnostic pathway for patients with haematological disorders, allowing discrimination between conditions of overlapping phenotypes therefore enabling more effective clinical t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47e359e69f447079b9255cd71870be26
https://doi.org/10.1182/blood-2018-99-118799
https://doi.org/10.1182/blood-2018-99-118799
Autor:
Peter Rushton, Claire Shooter, Xunde Wang, Andriani Kyrri, Barnaby Clark, Xenia Felekis, Marion Phylipsen, Miranda Petrou, Matthew Oakley, Chris Fisher, David Brawand, Frances Smith, Marina Kleanthous, Andrew M. Will, Helen Rooks, Laura Steedman, Douglas R. Higgs, Cornelius Harteveld, Swee Lay Thein, Anthi Drousiotou
Publikováno v:
Blood. 126:3375-3375
β thalassemia carriers are usually symptom free with microcytic hypochromic red cells and a raised HbA2 level. However, an increased output of α globin through co-inheritance of extra α globin genes, converts a typically asymptomatic β thalassemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49e6b1cd534a8088415e60b295dde128
https://doi.org/10.1182/blood.v126.23.3375.3375
https://doi.org/10.1182/blood.v126.23.3375.3375
Autor:
Christopher Wall, Margaret Allchurch, Matthew Oakley, Laura Steedman, Frances Smith, Peter Rushton, Swee Lay Thein, David C. Rees, David Brawand, Claire Hemmaway, Barnaby Clark, Keith Sibson
Publikováno v:
Blood. 126:946-946
Congenital anemia is difficult to diagnose once common causes have been excluded; for example 80% cases of congenital non-spherocytic hemolytic anemia are undiagnosed once pyruvate kinase and G6PD deficiencies have been excluded using phenotypic anal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::462b49759ef6c9ae940acee8a4bfb152
https://doi.org/10.1182/blood.v126.23.946.946
https://doi.org/10.1182/blood.v126.23.946.946
Autor:
Laura Steedman, Helen Rooks, Chris Fisher, Andriani Kyrri, Michael Hadjigavriel, Claire Shooter, Andrew M. Will, Xunde Wang, Swee Lay Thein, Douglas R. Higgs, Marina Kleanthous, Frances Smith, Cornelis L. Harteveld, Anthi Drousiotou, Marion Phylipsen, David Brawand, Barnaby Clark, Matthew Oakley, Peter Rushton
Publikováno v:
British Journal of Haematology
British Journal of Haematology, 180(1), 160-164
British Journal of Haematology, 180(1), 160-164
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89c63703ae4ca0eee9059d06f52bdd8d
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