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British Journal of Haematology|May 29, 2020
The pyruvate kinase (PK) to hexokinase enzyme activity ratio and erythrocyte PK protein level in the diagnosis and phenotype of PK deficiencyHanny Al-Samkari, Kathryn Addonizio, Bertil Glader, et al.
British Journal of Haematology|October 22, 2016
Increased prevalence of potential right-to-left shunting in children with sickle cell anaemia and strokeMichael M Dowling, Charles T Quinn, Claudio Ramaciotti, et al.
JAMA Neurology|October 31, 2012
Acute silent cerebral ischemic events in children with sickle cell anemiaCharles T Quinn, Robert C McKinstry, Michael M Dowling, et al.
The New England Journal of Medicine|December 13, 2021
Biologic and Clinical Efficacy of LentiGlobin for Sickle Cell DiseaseJulie Kanter, Mark C Walters, Lakshmanan Krishnamurti, et al.
British Journal of Haematology|April 25, 2015
Dysregulated arginine metabolism and cardiopulmonary dysfunction in patients with thalassaemiaClaudia R Morris, Hae-Young Kim, Elizabeth S Klings, et al.
Lancet (London, England)|November 11, 2024
Betibeglogene autotemcel gene therapy in patients with transfusion-dependent, severe genotype β-thalassaemia (HGB-212): a non-randomised, multicentre, single-arm, open-label, single-dose, phase 3 trialJanet L Kwiatkowski, Mark C Walters, Suradej Hongeng, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|January 29, 2018
Unrelated Donor Transplantation in Children with Thalassemia using Reduced-Intensity Conditioning: The URTH TrialShalini Shenoy, Mark C Walters, Alex Ngwube, et al.
Haematologica|April 16, 2013
Sildenafil therapy in thalassemia patients with Doppler-defined risk of pulmonary hypertensionClaudia R Morris, Hae-Young Kim, John Wood, et al.
The New England Journal of Medicine|September 5, 2019
Safety and Efficacy of Mitapivat in Pyruvate Kinase DeficiencyRachael F Grace, Christian Rose, D Mark Layton, et al.
American Journal of Hematology|December 1, 2015
Effects of hydroxyurea treatment for patients with hemoglobin SC diseaseLori Luchtman-Jones, Sara Pressel, Lee Hilliard, et al.
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