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Search results (9)

« Back to Publications

Prevalence and patterns of testing for anaemia in primary care in England: a cohort study using an electronic health records database.

Smith M. et al, (2025), Br J Gen Pract, 75, e232 - e240

Temporal changes in erythroid progenitors in critically ill patients: a prospective cohort study.

Scott C. et al, (2025), Haematologica, 110, 739 - 743

Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.

Gök V. et al, (2024), Br J Haematol, 205, 236 - 242

Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.

Scott C. et al, (2021), Haematologica, 106, 2960 - 2970

Genetic and functional insights into CDA-I prevalence and pathogenesis.

Olijnik A-A. et al, (2021), J Med Genet, 58, 185 - 195

Whole-genome sequencing of patients with rare diseases in a national health system

Turro E. et al, (2020), Nature, 583, 96 - 102

Single-cell O2 exchange imaging shows that cytoplasmic diffusion is a dominant barrier to efficient gas transport in red blood cells.

Richardson SL. et al, (2020), Proc Natl Acad Sci U S A, 117, 10067 - 10078

Single-cell analysis of bone marrow-derived CD34+ cells from children with sickle cell disease and thalassemia.

Hua P. et al, (2019), Blood, 134, 2111 - 2115

The management of anaemia and haematinic deficiencies in pregnancy and post-partum.

Roy NBA. and Pavord S., (2018), Transfus Med, 28, 107 - 116