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A proposed algorithm for evaluation and management of pediatric hemophilia patients who present to the emergency department with head trauma

Pediatric blood & cancer, 2022-09, Vol.69 (9), p.e29811-n/a

2022

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Improving an Administrative Case Definition for Longitudinal Surveillance of Sickle Cell Disease

Public health reports (1974), 2019-05, Vol.134 (3), p.274-281

2019

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Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease

Haematologica (Roma), 2020-12, Vol.105 (12), p.2887-2891

2020

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T Cell-Epstein-Barr Virus–Associated Hemophagocytic Lymphohistiocytosis (HLH) Occurs in Non-Asians and Is Associated with a T Cell Activation State that Is Comparable to Primary HLH

Journal of clinical immunology, 2021-10, Vol.41 (7), p.1582-1596

2021

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Decision-making about gene therapy in transfusion dependent thalassemia

BMC pediatrics, 2022-09, Vol.22 (1), p.536-536, Article 536

2022

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Correction to: T Cell‑Epstein‑Barr Virus–Associated Hemophagocytic Lymphohistiocytosis (HLH) Occurs in Non‑Asians and Is Associated with a T Cell Activation State that Is Comparable to Primary HLH

Journal of clinical immunology, 2021-11, Vol.41 (8), p.1979-1979

2021

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Hydroxyurea effectiveness in children and adolescents with sickle cell anemia: A large retrospective, population‐based cohort

American journal of hematology, 2017-01, Vol.92 (1), p.77-81

2017

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Patient and family experience with chronic transfusion therapy for sickle cell disease: A qualitative study

BMC pediatrics, 2020-04, Vol.20 (1), p.172-172, Article 172

2020

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Assessment of Patient and Caregiver Attitudes and Approaches to Decision-Making Regarding Bone Marrow Transplant for Sickle Cell Disease: A Qualitative Study

JAMA network open, 2020-05, Vol.3 (5), p.e206742-e206742

2020

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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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Contribution of alternative complement pathway to delayed hemolytic transfusion reaction in sickle cell disease

Haematologica (Roma), 2018-10, Vol.103 (10), p.e483-e485

2018

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Longitudinal Description of Gonadal Function in Sickle-cell Patients Treated With Hematopoietic Stem Cell Transplant Using Alkylator-based Conditioning Regimens

Journal of pediatric hematology/oncology, 2020-10, Vol.42 (7), p.e575

2020

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Lymphangiosarcoma of the thorax and thoracic vertebrae in a 16-year-old girl

Journal of clinical oncology, 2012-10, Vol.30 (29), p.e294-e298

2012

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Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia

Journal of pediatric hematology/oncology, 2016, Vol.38 (1), p.e32-e34

2016

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10-Year Mortality in Patients with Sickle Cell Disease from a Large Population-Based Cohort

Blood, 2020-11, Vol.136 (Supplement 1), p.56-56

2020

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Trends in Hospital Utilization for Acute Illness in a Large Population-Based Cohort of Children and Adolescents with Sickle Cell Disease (SCD): 2010–2017

Blood, 2018-11, Vol.132 (Supplement 1), p.3528-3528

2018

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Individualized, PK-Guided Dosing of Hydroxyurea Is Not Associated with Increased Hematologic Toxicity Compared to Weight-Based Initial Dosing: Interim Results from the Hops Trial

Blood, 2022-11, Vol.140 (Supplement 1), p.5416-5417

2022

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Effect of Acute Transfusion on Cerebral Oxygenation in Patients with Sickle Cell Disease

Blood, 2017-12, Vol.130 (Suppl_1), p.988-988

2017

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Inpatient Utilization Among Children and Adolescents with Sickle Cell Disease: Analysis of a Large Populated-Based Retrospective Cohort

Blood, 2015-12, Vol.126 (23), p.3262-3262

2015

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Accuracy of ICD-9 Coding for SCD in Children and Adolescents: Results from the Georgia (GA) Rush Surveillance Project

Blood, 2014-12, Vol.124 (21), p.4856-4856

2014

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Population-Based Analysis Of High Hospital Utilization (HHU) Among Children and Adolescents With Sickle Cell Disease (SCD)

Blood, 2013-11, Vol.122 (21), p.1740-1740

2013

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Hydroxyurea Effectiveness in Children and Adolescents with Sickle Cell Anemia: A Large Retrospective, Population-Based Cohort Study

Blood, 2015-12, Vol.126 (23), p.2179-2179

2015

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Volume regulation and KCl cotransport in reticulocyte populations of sickle and normal red blood cells

Blood cells, molecules, & diseases, 2011-08, Vol.47 (2), p.95-99

2011

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A Phase I Trial Of Zileuton In Sickle Cell Disease

Blood, 2013-11, Vol.122 (21), p.993-993

2013

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DEFINING A PHENOTYPE FOR RED CELL VOLUME REGULATION AND POTASSIUM CHLORIDE COTRANSPORT

Blood cells, molecules, & diseases, 2011-05, Vol.47 (2), p.95-99

2011

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A proposed algorithm for evaluation and management of pediatric hemophilia patients who present to the emergency department with head trauma

Improving an Administrative Case Definition for Longitudinal Surveillance of Sickle Cell Disease

Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease

T Cell-Epstein-Barr Virus–Associated Hemophagocytic Lymphohistiocytosis (HLH) Occurs in Non-Asians and Is Associated with a T Cell Activation State that Is Comparable to Primary HLH

Decision-making about gene therapy in transfusion dependent thalassemia

Correction to: T Cell‑Epstein‑Barr Virus–Associated Hemophagocytic Lymphohistiocytosis (HLH) Occurs in Non‑Asians and Is Associated with a T Cell Activation State that Is Comparable to Primary HLH

Hydroxyurea effectiveness in children and adolescents with sickle cell anemia: A large retrospective, population‐based cohort

Patient and family experience with chronic transfusion therapy for sickle cell disease: A qualitative study

Assessment of Patient and Caregiver Attitudes and Approaches to Decision-Making Regarding Bone Marrow Transplant for Sickle Cell Disease: A Qualitative Study

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

Contribution of alternative complement pathway to delayed hemolytic transfusion reaction in sickle cell disease

Longitudinal Description of Gonadal Function in Sickle-cell Patients Treated With Hematopoietic Stem Cell Transplant Using Alkylator-based Conditioning Regimens

Lymphangiosarcoma of the thorax and thoracic vertebrae in a 16-year-old girl

Hemoglobin F Only Syndrome at Birth: A Case of Maternal HbA2' Complicating the Diagnosis of β-Thalassemia

10-Year Mortality in Patients with Sickle Cell Disease from a Large Population-Based Cohort

Trends in Hospital Utilization for Acute Illness in a Large Population-Based Cohort of Children and Adolescents with Sickle Cell Disease (SCD): 2010–2017

Individualized, PK-Guided Dosing of Hydroxyurea Is Not Associated with Increased Hematologic Toxicity Compared to Weight-Based Initial Dosing: Interim Results from the Hops Trial

Effect of Acute Transfusion on Cerebral Oxygenation in Patients with Sickle Cell Disease

Inpatient Utilization Among Children and Adolescents with Sickle Cell Disease: Analysis of a Large Populated-Based Retrospective Cohort

Accuracy of ICD-9 Coding for SCD in Children and Adolescents: Results from the Georgia (GA) Rush Surveillance Project

Population-Based Analysis Of High Hospital Utilization (HHU) Among Children and Adolescents With Sickle Cell Disease (SCD)

Hydroxyurea Effectiveness in Children and Adolescents with Sickle Cell Anemia: A Large Retrospective, Population-Based Cohort Study

Volume regulation and KCl cotransport in reticulocyte populations of sickle and normal red blood cells

A Phase I Trial Of Zileuton In Sickle Cell Disease

DEFINING A PHENOTYPE FOR RED CELL VOLUME REGULATION AND POTASSIUM CHLORIDE COTRANSPORT

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