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Maintenance of a High Influenza Vaccination Rate and Improvement in Health Outcomes in a Pediatric Sickle Cell Disease Clinic

Journal of pediatric hematology/oncology, 2022-01, Vol.44 (1), p.e46

2022

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A comment on improving transcranial Doppler ultrasonography screening in children with sickle cell anemia

American journal of hematology, 2017-06, Vol.92 (6), p.E121-E122

2017

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Improvement in influenza vaccination rates in a pediatric sickle cell disease clinic

Pediatric blood & cancer, 2015-04, Vol.62 (4), p.654-657

2015

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A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy

Journal of pediatric hematology/oncology, 2018-04, Vol.40 (3), p.e145-e147

2018

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Measuring Transition Readiness of Young Adults with Sickle Cell Disease Using the Transition Readiness Assessment Questionnaire

Blood, 2016-12, Vol.128 (22), p.3534-3534

2016

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Health Care Utilization By Age and Hydroxyurea Response in Pediatric and Adolescent Patients with Sickle Cell Disease

Blood, 2016-12, Vol.128 (22), p.2500-2500

2016

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Beliefs about chelation among thalassemia patients

Health and quality of life outcomes, 2012-12, Vol.10 (1), p.148-148

2012

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Universal screening for social determinants of health in pediatric sickle cell disease: A quality‐improvement initiative

Pediatric blood & cancer, 2020-01, Vol.67 (1), p.e28006-n/a

2020

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Measuring transition readiness in adolescents and young adults with sickle cell disease using the transition readiness assessment questionnaire

Pediatric blood & cancer, 2022-02, Vol.69 (2), p.e29417-n/a

2022

Volltextzugriff (PDF)

Household material hardships impact emergency department reliance in pediatric patients with sickle cell disease

Pediatric blood & cancer, 2020-10, Vol.67 (10), p.e28587-n/a

2020

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How we prevent and manage infection in sickle cell disease

British journal of haematology, 2015-09, Vol.170 (6), p.757-767

2015

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Rethinking Rideshares: A Transportation Assistance Pilot for Pediatric Patients with Sickle Cell Disease

Journal of health care for the poor and underserved, 2020-08, Vol.31 (3), p.1457

2020

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Initial outcomes in a sickle cell disease transition clinic

Health Care Transitions, 2024, Vol.2, p.100056, Article 100056

2024

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Developing a Problem-Solving Intervention to Address Methods of Self-Management and Transition Challenges in Adolescents with Sickle Cell Disease: A Qualitative Investigation

Blood, 2017-12, Vol.130, p.2081-2081

2017

Volltextzugriff (PDF)

Two Sides of a Coin: Case Report of Unilateral Synangiosis and Contralateral Stroke Highlighting Consequences of Disease Progression and Efficacy of Revascularization in Sickle Cell Disease-Associated Moyamoya Syndrome

Acta haematologica, 2022-07, Vol.145 (4), p.458-464

2022

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Using Reticulocyte Hemoglobin Equivalent to Screen for Iron Deficiency May Be Problematic

Global pediatric health, 2014, Vol.1, p.2333794X14557030-2333794X14557030

2014

Volltextzugriff (PDF)

Improving the Management of Vaso-Occlusive Episodes in the Pediatric Emergency Department

Pediatrics (Evanston), 2015-10, Vol.136 (4), p.e1016

2015

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Developing a Problem-solving Intervention to Improve Self-Management and Transition Readiness in Adolescents with Sickle Cell Disease

Journal of pediatric nursing, 2019-05, Vol.46, p.26-32

2019

Volltextzugriff (PDF)

Recognition and Management of Immune Thrombocytopenic Purpura and Autoimmune Hemolytic Anemia in the Emergency Department

Clinical pediatric emergency medicine, 2011-09, Vol.12 (3), p.245-252

2011

Volltextzugriff (PDF)

A comment on improving transcranial D oppler ultrasonography screening in children with sickle cell anemia

American journal of hematology, 2017-06, Vol.92 (6)

2017

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Optimizing Shared Decision Making about Hydroxyurea in Young Children with Sickle Cell Anemia

Blood, 2022-11, Vol.140 (Supplement 1), p.10857-10859

2022

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Self-reported transition readiness among young adults with sickle cell disease

Journal of pediatric hematology/oncology, 2014-07, Vol.36 (5), p.389-394

2014

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Relationship among chelator adherence, change in chelators, and quality of life in Thalassemia

Quality of life research, 2014-10, Vol.23 (8), p.2277-2288

2014

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Transition from pediatric to adult care for sickle cell disease: Results of a survey of pediatric providers

American journal of hematology, 2011-06, Vol.86 (6), p.512-515

2011

Volltextzugriff (PDF)

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Maintenance of a High Influenza Vaccination Rate and Improvement in Health Outcomes in a Pediatric Sickle Cell Disease Clinic

A comment on improving transcranial Doppler ultrasonography screening in children with sickle cell anemia

Improvement in influenza vaccination rates in a pediatric sickle cell disease clinic

A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy

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

Measuring Transition Readiness of Young Adults with Sickle Cell Disease Using the Transition Readiness Assessment Questionnaire

Health Care Utilization By Age and Hydroxyurea Response in Pediatric and Adolescent Patients with Sickle Cell Disease

Beliefs about chelation among thalassemia patients

Universal screening for social determinants of health in pediatric sickle cell disease: A quality‐improvement initiative

Measuring transition readiness in adolescents and young adults with sickle cell disease using the transition readiness assessment questionnaire

Household material hardships impact emergency department reliance in pediatric patients with sickle cell disease

How we prevent and manage infection in sickle cell disease

Rethinking Rideshares: A Transportation Assistance Pilot for Pediatric Patients with Sickle Cell Disease

Initial outcomes in a sickle cell disease transition clinic

Developing a Problem-Solving Intervention to Address Methods of Self-Management and Transition Challenges in Adolescents with Sickle Cell Disease: A Qualitative Investigation

Two Sides of a Coin: Case Report of Unilateral Synangiosis and Contralateral Stroke Highlighting Consequences of Disease Progression and Efficacy of Revascularization in Sickle Cell Disease-Associated Moyamoya Syndrome

Using Reticulocyte Hemoglobin Equivalent to Screen for Iron Deficiency May Be Problematic

Improving the Management of Vaso-Occlusive Episodes in the Pediatric Emergency Department

Developing a Problem-solving Intervention to Improve Self-Management and Transition Readiness in Adolescents with Sickle Cell Disease

Recognition and Management of Immune Thrombocytopenic Purpura and Autoimmune Hemolytic Anemia in the Emergency Department

A comment on improving transcranial D oppler ultrasonography screening in children with sickle cell anemia

Optimizing Shared Decision Making about Hydroxyurea in Young Children with Sickle Cell Anemia

Self-reported transition readiness among young adults with sickle cell disease

Relationship among chelator adherence, change in chelators, and quality of life in Thalassemia

Transition from pediatric to adult care for sickle cell disease: Results of a survey of pediatric providers

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