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Displaying 1-20 of 28 total results
1.
Children and Their Families Have a Right to Gender-Affirming Healthcare
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
11.
Continuing Sickle Cell Disease Care During the COVID-19 Pandemic
12.
Four Solutions for Sickle Cell Disease Support
13.
Disseminating Results: Missed Sickle Cell Disease Clinic Appointments and the Health Belief Model
14.
Rare Diseases Deserve Our Attention
15.
Improving Transitions in Care Saves Lives
16.
An Innovation in Provider Training Increases Access to Care for Sickle Cell Disease Patients
17.
Recent Legislation that Supports Better Children’s Health Outcomes
18.
What’s Next for Sickle Cell Disease Improvement? Three Areas That Still Need Our Attention
19.
Start Producing Better Sickle Cell Disease Outcomes in Your Community Today
20.
Creating Better Advocates for Sickle Cell Disease Care
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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
(6)
Sickle Cell Disease Newborn Screening Program
(3)
Working to Improve Sickle Cell Healthcare (WISCH)
(2)
Disseminating Results: Missed Sickle Cell Disease Clinic Appointments and the Health Belief Model
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Hemoglobinopathies National Coordinating Center (HNCC)
(1)
National Network of Perinatal Quality Collaboratives (2017 - 2022)
(1)
New York State Maternal and Child Health Collaboratives
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