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ERJ Open Research
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December 2, 2020
Beneficial effects of adenotonsillectomy in children with sickle cell disease
Ilaria Liguoro, Michele Arigliani, Bethany Singh, et al.
American Journal of Hematology
|
June 26, 2025
Loss of Function SPTA1 Variants Causes Neonatal Liver Failure and Fetal Anemia
John Brewin, Barnaby Clark, Frances Smith, et al.
Plos One
|
August 16, 2019
Improving low fruit and vegetable intake in children: Findings from a system dynamics, community group model building study
Sarah Gerritsen, Ana Renker-Darby, Sophia Harré, et al.
Scientific Reports
|
July 14, 2019
Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri Lanka
Shiromi Perera, Angela Allen, Ishari Silva, et al.
Free Radical Biology & Medicine
|
March 7, 2021
Oxidative status in the β-thalassemia syndromes in Sri Lanka; a cross-sectional survey
Angela Allen, Shiromi Perera, Sachith Mettananda, et al.
Hemasphere
|
March 14, 2025
Selecting patients with sickle cell disease for gene addition or gene editing-based therapeutic approaches: Report on behalf of a joint EHA Specialized Working Group and EBMT Hemoglobinopathies Working Party consensus conference
Lucia de Franceschi, Franco Locatelli, David Rees, et al.
Hemasphere
|
June 26, 2025
Fetal-hemoglobin-expressing red blood cells ("F cells") consist of three distinct types as revealed by single-cell transcriptomic analysis of circulating reticulocytes
Helen Rooks, Cecilia Ng, Spyros Oikonomopoulos, et al.
British Journal of Haematology
|
March 6, 2019
Index of Pain Experience in Sickle Cell Anaemia (IPESCA): development from daily pain diaries and initial findings from use with children and adults with sickle cell anaemia
Jamie M Kawadler, April Slee, Hanne Stotesbury, et al.
British Journal of Haematology
|
June 6, 2022
The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper
Noémi B A Roy, Lydie Da Costa, Roberta Russo, et al.
Hemasphere
|
June 10, 2022
The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper
Noémi B A Roy, Lydie Da Costa, Roberta Russo, et al.
Page
of 14
Search research articles
Search
Showing results (121-130 of 140) with videos related to
Sort By:
Page
of 14
ERJ Open Research
|
December 2, 2020
Beneficial effects of adenotonsillectomy in children with sickle cell disease
Ilaria Liguoro, Michele Arigliani, Bethany Singh, et al.
American Journal of Hematology
|
June 26, 2025
Loss of Function SPTA1 Variants Causes Neonatal Liver Failure and Fetal Anemia
John Brewin, Barnaby Clark, Frances Smith, et al.
Plos One
|
August 16, 2019
Improving low fruit and vegetable intake in children: Findings from a system dynamics, community group model building study
Sarah Gerritsen, Ana Renker-Darby, Sophia Harré, et al.
Scientific Reports
|
July 14, 2019
Genotype-phenotype association analysis identifies the role of α globin genes in modulating disease severity of β thalassaemia intermedia in Sri Lanka
Shiromi Perera, Angela Allen, Ishari Silva, et al.
Free Radical Biology & Medicine
|
March 7, 2021
Oxidative status in the β-thalassemia syndromes in Sri Lanka; a cross-sectional survey
Angela Allen, Shiromi Perera, Sachith Mettananda, et al.
Hemasphere
|
March 14, 2025
Selecting patients with sickle cell disease for gene addition or gene editing-based therapeutic approaches: Report on behalf of a joint EHA Specialized Working Group and EBMT Hemoglobinopathies Working Party consensus conference
Lucia de Franceschi, Franco Locatelli, David Rees, et al.
Hemasphere
|
June 26, 2025
Fetal-hemoglobin-expressing red blood cells ("F cells") consist of three distinct types as revealed by single-cell transcriptomic analysis of circulating reticulocytes
Helen Rooks, Cecilia Ng, Spyros Oikonomopoulos, et al.
British Journal of Haematology
|
March 6, 2019
Index of Pain Experience in Sickle Cell Anaemia (IPESCA): development from daily pain diaries and initial findings from use with children and adults with sickle cell anaemia
Jamie M Kawadler, April Slee, Hanne Stotesbury, et al.
British Journal of Haematology
|
June 6, 2022
The use of next-generation sequencing in the diagnosis of rare inherited anaemias: A Joint BSH/EHA Good Practice Paper
Noémi B A Roy, Lydie Da Costa, Roberta Russo, et al.
Hemasphere
|
June 10, 2022
The Use of Next-generation Sequencing in the Diagnosis of Rare Inherited Anaemias: A Joint BSH/EHA Good Practice Paper
Noémi B A Roy, Lydie Da Costa, Roberta Russo, et al.
Page
of 14