Detalhe da pesquisa
1.
The genetic dissection of fetal haemoglobin persistence in sickle cell disease in Nigeria.
Hum Mol Genet
; 33(10): 919-929, 2024 May 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38339995
2.
Males with sickle cell disease have higher risks of cerebrovascular disease, increased inflammation, and a reduced response to hydroxyurea.
Am J Hematol
; 98(11): E341-E344, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37646569
3.
Oxygen gradient ektacytometry does not predict pain in children with sickle cell anaemia.
Br J Haematol
; 197(5): 609-617, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34859420
4.
Measurement of erythrocyte membrane mannoses to assess splenic function.
Br J Haematol
; 198(1): 155-164, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35411940
5.
The significance of spleen size in children with sickle cell anemia.
Am J Hematol
; 97(12): 1520-1528, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36054667
6.
The pleiotropic effects of α-thalassemia on HbSS and HbSC sickle cell disease: Reduced erythrocyte cation co-transport activity, serum erythropoietin, and transfusion burden, do not translate into increased survival.
Am J Hematol
; 97(10): 1275-1285, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35802781
7.
Recovery Colleges Characterisation and Testing in England (RECOLLECT): rationale and protocol.
BMC Psychiatry
; 22(1): 627, 2022 09 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36153488
8.
Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC).
Haematologica
; 106(6): 1770-1773, 2021 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33353285
9.
The role of WNK in modulation of KCl cotransport activity in red cells from normal individuals and patients with sickle cell anaemia.
Pflugers Arch
; 471(11-12): 1539-1549, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31729557
10.
The effects of hydroxycarbamide on the plasma proteome of children with sickle cell anaemia.
Br J Haematol
; 186(6): 879-886, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31140594
11.
Oxidative stress and phosphatidylserine exposure in red cells from patients with sickle cell anaemia.
Br J Haematol
; 182(4): 567-578, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29938778
12.
Proteomic analysis of plasma from children with sickle cell anemia and silent cerebral infarction.
Haematologica
; 103(7): 1136-1142, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29545349
13.
How I manage sickle cell patients with high transcranial doppler results.
Br J Haematol
; 179(3): 377-388, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28771666
14.
The super sickling haemoglobin HbS-Oman: a study of red cell sickling, K+ permeability and associations with disease severity in patients heterozygous for HbA and HbS-Oman (HbA/S-Oman genotype).
Br J Haematol
; 179(2): 256-265, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28699687
15.
A novel index to evaluate ineffective erythropoiesis in hematological diseases offers insights into sickle cell disease.
Haematologica
; 107(1): 338-341, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34670360
16.
Catheter associated thromboses in patients with sickle cell anaemia and dual lumen Vortex apheresis ports are common and can be clinically asymptomatic.
Br J Haematol
; 189(5): e198-e200, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32207154
17.
A gain of function variant in PIEZO1 (E756del) and sickle cell disease.
Haematologica
; 104(3): e91-e93, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30237267
18.
Human cellular model systems of ß-thalassemia enable in-depth analysis of disease phenotype.
Nat Commun
; 14(1): 6260, 2023 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37803026
19.
Determinants of severity in sickle cell disease.
Blood Rev
; 56: 100983, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35750558
20.
The erythrocyte membrane properties of beta thalassaemia heterozygotes and their consequences for Plasmodium falciparum invasion.
Sci Rep
; 12(1): 8934, 2022 05 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35624125