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British Journal of Haematology
|
May 27, 2005
Childhood essential thrombocythaemia
Noemi B A Roy, Marilyn Treacy, Peter Kench
British Journal of Haematology
|
February 21, 2022
Expanded eligibility for emerging therapies in sickle cell disease in the UK - crizanlizumab and voxelotor
Sona M Vora, Stephen Boyd, Nicholas Denny, et al.
British Journal of Haematology
|
December 6, 2008
The role of X-inactivation in the gender bias of patients with acquired alpha-thalassaemia and myelodysplastic syndrome (ATMDS)
Peter S Haas, Noemi B A Roy, Richard J Gibbons, et al.
Haematologica
|
October 4, 2024
Temporal changes in erythroid progenitors in critically ill patients: a prospective cohort study
Caroline Scott, Isabella Dale-Harris, Andrew E Armitage, et al.
Nature Communications
|
April 19, 2023
Direct correction of haemoglobin E β-thalassaemia using base editors
Mohsin Badat, Ayesha Ejaz, Peng Hua, et al.
Blood Global Hematology
|
February 25, 2026
Urinary carbonic anhydrase 1 excretion is a marker of hemolysis-triggering conditions suitable for point-of-care testing
Alzbeta Hulikova, Zhenyi Wang, Helen Broomfield, et al.
Journal of the Intensive Care Society
|
November 17, 2025
Anaemia management with red blood cell transfusion to improve post-intensive care disability: Protocol for the ABC post-ICU randomised controlled trial
Timothy S Walsh, Lydia Emerson, Jo Singleton, et al.
Haematologica
|
October 30, 2020
Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities
Caroline Scott, Damien J Downes, Jill M Brown, et al.
British Journal of Haematology
|
May 29, 2024
Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants
Veysel Gök, Göksel Leblebisatan, Dilek Gürlek Gökçebay, et al.
Nature
|
June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health system
Ernest Turro, William J Astle, Karyn Megy, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
British Journal of Haematology
|
May 27, 2005
Childhood essential thrombocythaemia
Noemi B A Roy, Marilyn Treacy, Peter Kench
British Journal of Haematology
|
February 21, 2022
Expanded eligibility for emerging therapies in sickle cell disease in the UK - crizanlizumab and voxelotor
Sona M Vora, Stephen Boyd, Nicholas Denny, et al.
British Journal of Haematology
|
December 6, 2008
The role of X-inactivation in the gender bias of patients with acquired alpha-thalassaemia and myelodysplastic syndrome (ATMDS)
Peter S Haas, Noemi B A Roy, Richard J Gibbons, et al.
Haematologica
|
October 4, 2024
Temporal changes in erythroid progenitors in critically ill patients: a prospective cohort study
Caroline Scott, Isabella Dale-Harris, Andrew E Armitage, et al.
Nature Communications
|
April 19, 2023
Direct correction of haemoglobin E β-thalassaemia using base editors
Mohsin Badat, Ayesha Ejaz, Peng Hua, et al.
Blood Global Hematology
|
February 25, 2026
Urinary carbonic anhydrase 1 excretion is a marker of hemolysis-triggering conditions suitable for point-of-care testing
Alzbeta Hulikova, Zhenyi Wang, Helen Broomfield, et al.
Journal of the Intensive Care Society
|
November 17, 2025
Anaemia management with red blood cell transfusion to improve post-intensive care disability: Protocol for the ABC post-ICU randomised controlled trial
Timothy S Walsh, Lydia Emerson, Jo Singleton, et al.
Haematologica
|
October 30, 2020
Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities
Caroline Scott, Damien J Downes, Jill M Brown, et al.
British Journal of Haematology
|
May 29, 2024
Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants
Veysel Gök, Göksel Leblebisatan, Dilek Gürlek Gökçebay, et al.
Nature
|
June 26, 2020
Whole-genome sequencing of patients with rare diseases in a national health system
Ernest Turro, William J Astle, Karyn Megy, et al.
Page
of 2