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Displaying 1-20 of 32 total results
1.
Enhanced Support During and After Transition from Pediatric to Adult Care Needed for People Living with Sickle Cell Disease
2.
3 Ways to Close Gaps in Sickle Cell Disease Care: Recommendations from NICHQ Projects
3.
NICHQ Intern Spotlight: Macy Parakh
4.
NICHQ Intern Spotlight: Madeline D’Onfro
5.
NICHQ Intern Spotlight: Lyndsay Brooks
6.
NICHQ Intern Spotlight: Elyse Anderson
7.
NICHQ Intern Spotlight: Lucia (Lucy) Burzynski
8.
Hemoglobinopathies National Coordinating Center (HNCC)
9.
A Physician’s Reflections on Racism and Treating Sickle Cell Disease
10.
NICHQ Employee Spotlight: Kim Sprunck
14.
Continuing Sickle Cell Disease Care During the COVID-19 Pandemic
15.
Four Solutions for Sickle Cell Disease Support
16.
Disseminating Results: Missed Sickle Cell Disease Clinic Appointments and the Health Belief Model
17.
Rare Diseases Deserve Our Attention
18.
Improving Transitions in Care Saves Lives
19.
An Innovation in Provider Training Increases Access to Care for Sickle Cell Disease Patients
20.
Recent Legislation that Supports Better Children’s Health Outcomes
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Sickle Cell Disease Treatment Demonstration Regional Collaboratives Program National Coordinating Center
(13)
Content Development for Newborn Screening Clearinghouse
(7)
Sickle Cell Disease Treatment Demonstration Program
(7)
Disseminating Results: Missed Sickle Cell Disease Clinic Appointments and the Health Belief Model
(4)
Sickle Cell Disease Newborn Screening Program
(3)
Hemoglobinopathies National Coordinating Center (HNCC)
(2)
Working to Improve Sickle Cell Healthcare (WISCH)
(2)
National Network of Perinatal Quality Collaboratives (2017 - 2022)
(1)
New York State Maternal and Child Health Collaboratives
(1)