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Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia

Trials, 2020-11, Vol.21 (1), p.1-14, Article 983

2020

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LIN28A expression reduces sickling of cultured human erythrocytes

PloS one, 2014-09, Vol.9 (9), p.e106924-e106924

2014

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Iron dose-dependent differentiation and enucleation of human erythroblasts in serum-free medium

Journal of tissue engineering and regenerative medicine, 2016-02, Vol.10 (2), p.E84-E89

2016

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A synthetic model of human beta-thalassemia erythropoiesis using CD34+ cells from healthy adult donors

PloS one, 2013-07, Vol.8 (7), p.e68307-e68307

2013

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Hydroxyurea therapy in sickle cell disease: An alternative approach to preoperative red cell transfusion

Journal of the National Medical Association, 2015-06, Vol.107 (2), p.102-103

2015

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A Randomized Controlled Trial of Working Memory Training in Pediatric Sickle Cell Disease

Journal of pediatric psychology, 2021-09, Vol.46 (8), p.1001-1014

2021

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LIN28B-mediated expression of fetal hemoglobin and production of fetal-like erythrocytes from adult human erythroblasts ex vivo

Blood, 2013-08, Vol.122 (6), p.1034-1041

2013

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A Feasibility Pilot Study of Online Modules of Hydroxyurea and Sickle Cell Disease Care for Adolescents and Young Adults for Family Medicine Residents

Journal of pediatric hematology/oncology, 2022-03, Vol.44 (2), p.e313-e318

2022

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Acceptable, hopeful, and useful: development and mixed-method evaluation of an educational tool about reproductive options for people with sickle cell disease or trait

Journal of assisted reproduction and genetics, 2022-01, Vol.39 (1), p.183-193

2022

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Identification and Clinical Characterization of Children With Benign Ethnic Neutropenia

Journal of pediatric hematology/oncology, 2016-04, Vol.38 (3), p.e140-e143

2016

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Improving Outcomes for Patients With Sickle Cell Disease in the United States: Making the Case for More Resources, Surveillance, and Longitudinal Data

JAMA health forum, 2021-10, Vol.2 (10), p.e213467-e213467

2021

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Cerebral vasculopathy in children with sickle cell anemia

Blood cells, molecules, & diseases, 2015-01, Vol.54 (1), p.17-25

2015

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Feasibility of Home-Based Computerized Working Memory Training With Children and Adolescents With Sickle Cell Disease

Pediatric blood & cancer, 2016-09, Vol.63 (9), p.1578-1585

2016

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Unruptured Intracranial Aneurysms in Children With Sickle Cell Disease: Analysis of 18 Aneurysms in 5 Patients

Neurosurgery, 2015-05, Vol.76 (5), p.531-539

2015

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Distinct Ldb1/NLI complexes orchestrate γ-globin repression and reactivation through ETO2 in human adult erythroid cells

Blood, 2011-12, Vol.118 (23), p.6200-6208

2011

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Measuring Transition Readiness: A Correlational Study of Perceptions of Parent and Adolescents and Young Adults with Sickle Cell Disease

Journal of pediatric nursing, 2015-09, Vol.30 (5), p.788-796

2015

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Early career mentoring through the American Society of Pediatric Hematology/Oncology: Lessons learned from a pilot program

Pediatric blood & cancer, 2017-03, Vol.64 (3), p.np-n/a

2017

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Sickle cell disease related internet activity is three times less frequent than cystic fibrosis related internet activity

Pediatric blood & cancer, 2016-11, Vol.63 (11), p.2061-2062

2016

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Children with sickle cell anemia with normal transcranial Doppler ultrasounds and without silent infarcts have a low incidence of new strokes

American journal of hematology, 2018-06, Vol.93 (6), p.760-768

2018

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Iron dose‐dependent differentiation and enucleation of human erythroblasts in serum‐free medium

Journal of tissue engineering and regenerative medicine, 2016-02, Vol.10 (2), p.E84-E89

2016

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Inflammatory Bowel Disease in Sickle Cell Disease: Diagnostic and Treatment Challenges

Journal of pediatric gastroenterology and nutrition, 2014-11, Vol.59 (5), p.e47-e47

2014

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Anaplastic Ependymoma in a Child With Sickle Cell Anemia: A Case Report Highlighting Treatment Challenges for Young Children With Central Nervous System Tumors and Underlying Vasculopathy

Pediatric blood & cancer, 2016-03, Vol.63 (3), p.547-550

2016

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Cytokine-mediated increases in fetal hemoglobin are associated with globin gene histone modification and transcription factor reprogramming

Blood, 2009-09, Vol.114 (11), p.2299-2306

2009

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Clinical and Geographic Characterization of 30-Day Readmissions in Pediatric Sickle Cell Crisis Patients

Hospital pediatrics, 2015-08, Vol.5 (8), p.423-431

2015

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Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia

LIN28A expression reduces sickling of cultured human erythrocytes

Iron dose-dependent differentiation and enucleation of human erythroblasts in serum-free medium

A synthetic model of human beta-thalassemia erythropoiesis using CD34+ cells from healthy adult donors

Hydroxyurea therapy in sickle cell disease: An alternative approach to preoperative red cell transfusion

A Randomized Controlled Trial of Working Memory Training in Pediatric Sickle Cell Disease

LIN28B-mediated expression of fetal hemoglobin and production of fetal-like erythrocytes from adult human erythroblasts ex vivo

A Feasibility Pilot Study of Online Modules of Hydroxyurea and Sickle Cell Disease Care for Adolescents and Young Adults for Family Medicine Residents

Acceptable, hopeful, and useful: development and mixed-method evaluation of an educational tool about reproductive options for people with sickle cell disease or trait

Identification and Clinical Characterization of Children With Benign Ethnic Neutropenia

Improving Outcomes for Patients With Sickle Cell Disease in the United States: Making the Case for More Resources, Surveillance, and Longitudinal Data

Cerebral vasculopathy in children with sickle cell anemia

Feasibility of Home-Based Computerized Working Memory Training With Children and Adolescents With Sickle Cell Disease

Unruptured Intracranial Aneurysms in Children With Sickle Cell Disease: Analysis of 18 Aneurysms in 5 Patients

Distinct Ldb1/NLI complexes orchestrate γ-globin repression and reactivation through ETO2 in human adult erythroid cells

Measuring Transition Readiness: A Correlational Study of Perceptions of Parent and Adolescents and Young Adults with Sickle Cell Disease

Early career mentoring through the American Society of Pediatric Hematology/Oncology: Lessons learned from a pilot program

Sickle cell disease related internet activity is three times less frequent than cystic fibrosis related internet activity

Children with sickle cell anemia with normal transcranial Doppler ultrasounds and without silent infarcts have a low incidence of new strokes

Iron dose‐dependent differentiation and enucleation of human erythroblasts in serum‐free medium

Inflammatory Bowel Disease in Sickle Cell Disease: Diagnostic and Treatment Challenges

Anaplastic Ependymoma in a Child With Sickle Cell Anemia: A Case Report Highlighting Treatment Challenges for Young Children With Central Nervous System Tumors and Underlying Vasculopathy

Cytokine-mediated increases in fetal hemoglobin are associated with globin gene histone modification and transcription factor reprogramming

Engaging Caregivers and Providers of Children With Sickle Cell Anemia in Shared Decision Making for Hydroxyurea: Protocol for a Multicenter Randomized Controlled Trial

Clinical and Geographic Characterization of 30-Day Readmissions in Pediatric Sickle Cell Crisis Patients

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