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Author Details
Full Name
Andrew D Campbell
Affiliation
Departments of Hematology at Children's National Hospital
ORCID
Career Start Year
1996
Papers
80
H Index
26
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36698745
Design of an adaptive randomized clinical trial of intravenous citrulline for sickle cell pain crisis in the emergency department.
Contemp Clin Trials Commun
2023
37458568
Return visit rates after an emergency department discharge for children with sickle cell pain episodes.
Pediatr Blood Cancer
2023
37217303
The evolution of the COVID-19 pandemic in paediatric patients with sickle cell disease: From Alpha to Omicron.
Br J Haematol
2023
36873869
Clinical outcomes of children and adolescents with sickle cell disease and COVID-19 infection: A year in review at a metropolitan tertiary pediatric hospital.
Front Med (Lausanne)
2023
35166851
Pain Burden in the CASiRe International Cohort of Sickle Cell Patients: United States and Ghana.
Pain Med
2022
35451176
Safety and efficacy of voxelotor in pediatric patients with sickle cell disease aged 4 to 11Â years.
Pediatr Blood Cancer
2022
36030599
Amino acid signature during sickle cell pain crisis shows significant alterations related to nitric oxide and energy metabolism.
Mol Genet Metab
2022
33401140
Age of first pain crisis and associated complications in the CASiRe international sickle cell disease cohort.
Blood Cells Mol Dis
2021
33838114
Will the changing therapeutic landscape meet the needs of patients with sickle cell disease?
Lancet Haematol
2021
34530179
Low Rates of Cerebral Infarction after Hematopoietic Stem Cell Transplantation in Patients with Sickle Cell Disease at High Risk for Stroke.
Transplant Cell Ther
2021
34548040
Diagnosis patterns of sickle cell disease in Ghana: a secondary analysis.
BMC Public Health
2021
34564050
Global geographic differences in healthcare utilization for sickle cell disease pain crises in the CASiRe cohort.
Blood Cells Mol Dis
2021
34002408
Screening for new red blood cell alloantibodies after transfusion in patients with sickle cell disease.
Transfusion
2021
32131139
Parvovirus B19 infection in sickle cell disease: An analysis from the Centers for Disease Control haemoglobinopathy blood surveillance project.
Transfus Med
2020
33323100
Annual Academy of Sickle Cell and Thalassaemia (ASCAT) conference: a summary of the proceedings.
BMC Proc
2020
32972798
Corrigendum to "Protective effect of HLA-DQB1 alleles against alloimmunization in patients with sickle cell disease" [Hum. Immunol. (2016) 35-40].
Hum Immunol
2020
32597290
The Economic Burden of End-Organ Damage Among Medicaid Patients with Sickle Cell Disease in the United States: A Population-Based Longitudinal Claims Study.
J Manag Care Spec Pharm
2020
32706890
Influence of single parenthood on cardiopulmonary function in pediatric patients with sickle cell anemia.
Blood Adv
2020
33021900
The Sickle Cell Disease Ontology: Enabling Collaborative Research and Co-Designing of New Planetary Health Applications.
OMICS
2020
32697331
The CYB5R3<sup>c</sup> <sup>.350C>G</sup> and G6PD A alleles modify severity of anemia in malaria and sickle cell disease.
Am J Hematol
2020
32243618
Tricuspid regurgitation velocity and other biomarkers of mortality in children, adolescents and young adults with sickle cell disease in the United States: The PUSH study.
Am J Hematol
2020
32170816
Correlation of lipid peroxidation and nitric oxide metabolites, trace elements, and antioxidant enzymes in patients with sickle cell disease.
J Clin Lab Anal
2020
32377816
A study of the geographic distribution and associated risk factors of leg ulcers within an international cohort of sickle cell disease patients: the CASiRe group analysis.
Ann Hematol
2020
29411862
A phase 1 dose-finding study of intravenous L-citrulline in sickle cell disease: a potential novel therapy for sickle cell pain crisis.
Br J Haematol
2019
31469310
Identifying Clinical and Research Priorities in Sickle Cell Lung Disease. An Official American Thoracic Society Workshop Report.
Ann Am Thorac Soc
2019
31117252
Serum Iron Levels and Copper-to-Zinc Ratio in Sickle Cell Disease.
Medicina (Kaunas)
2019
30758856
Red blood cell alloimmunization and minor red blood cell antigen phenotypes in transfused Ghanaian patients with sickle cell disease.
Transfusion
2019
28801954
An analysis of inpatient pediatric sickle cell disease: Incidence, costs, and outcomes.
Pediatr Blood Cancer
2018
30233199
Low nitric oxide level is implicated in sickle cell disease and its complications in Ghana.
Vasc Health Risk Manag
2018
29954157
Elevated Proangiogenic Markers are Associated with Vascular Complications within Ghanaian Sickle Cell Disease Patients.
Med Sci (Basel)
2018
30577523
Correlation Between Soluble Endothelial Adhesion Molecules and Nitric Oxide Metabolites in Sickle Cell Disease.
Med Sci (Basel)
2018
29455883
Disseminated Intravascular Coagulation and Acute Liver Injury from Ethanol Embolization of an Arteriovenous Malformation.
J Vasc Interv Radiol
2018
27030515
mTOR Inhibition improves anaemia and reduces organ damage in a murine model of sickle cell disease.
Br J Haematol
2016
26613837
Hematologic outcomes after total splenectomy and partial splenectomy for congenital hemolytic anemia.
J Pediatr Surg
2016
26476208
Protective effect of HLA-DQB1 alleles against alloimmunization in patients with sickle cell disease.
Hum Immunol
2016
26372199
Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.
Hemoglobin
2016
26500093
Indications and Results of HLA-Identical Sibling Hematopoietic Cell Transplantation for Sickle Cell Disease.
Biol Blood Marrow Transplant
2016
27354937
Proceedings of a Sickle Cell Disease Ontology workshop - Towards the first comprehensive ontology for Sickle Cell Disease.
Appl Transl Genom
2016
26771086
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotes.
Br J Haematol
2016
25382665
Clinical outcomes of splenectomy in children: report of the splenectomy in congenital hemolytic anemia registry.
Am J Hematol
2015
26460253
TR2/TR4 overexpression in a humanized sickle cell disease mouse model decreases RBC adhesion to VCAM-1.
Blood Cells Mol Dis
2015
26296885
Intestine-specific Disruption of Hypoxia-inducible Factor (HIF)-2α Improves Anemia in Sickle Cell Disease.
J Biol Chem
2015
26161296
Melanoma tumor growth is accelerated in a mouse model of sickle cell disease.
Exp Hematol Oncol
2015
26031919
The LSD1 inhibitor RN-1 induces fetal hemoglobin synthesis and reduces disease pathology in sickle cell mice.
Blood
2015
25561507
Compound loss of function of nuclear receptors Tr2 and Tr4 leads to induction of murine embryonic β-type globin genes.
Blood
2015
24361300
Differences in the clinical and genotypic presentation of sickle cell disease around the world.
Paediatr Respir Rev
2014
24662048
PGC-1 coactivator activity is required for murine erythropoiesis.
Mol Cell Biol
2014
24652968
Increased stroke size following MCA occlusion in a mouse model of sickle cell disease.
Blood
2014
24309610
Abnormal pulmonary function and associated risk factors in children and adolescents with sickle cell anemia.
J Pediatr Hematol Oncol
2014
22903793
Who counsels parents of newborns who are carriers of sickle cell anemia or cystic fibrosis?
J Genet Couns
2013
1 - 50 of 80
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Co-authored papers
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Co-authored papers
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Universite de Strasbourg
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University of California San Francisco
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Vanderbilt University School of Medicine
Co-authored papers
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Caribbean Institute for Health Research, The University of the West Indies
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Loyola University Medical Center.
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Unidade de Onco-Hematologia, Instituto da Crianca
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Kofi A Anie
London North West University Healthcare NHS Trust, Imperial College London
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