by Stella T. Chou, MD; Michael Rutledge DeBaun, MD, MPH; and Julie Kanter, MD
Patients with sickle cell disease (SCD) require regular follow-up throughout their entire lives. Unfortunately, many of these individuals do not ha......READ MORE
by Stella T. Chou, MD; Michael Rutledge DeBaun, MD, MPH; and Julie Kanter, MD
A multipronged approach may help reduce the frequency of pain events that can lead to hospitalizations in patients with sickle cell disease (SCD). ......READ MORE
Patients with sickle cell disease (SCD) experience extremely severe and debilitating acute and chronic pain. Efforts to successfully treating that ......READ MORE
Patients with sickle cell disease (SCD) and acute vaso-occlusive crises experience pain that can be debilitating. A multidisciplinary approach may ......READ MORE
Acute chest syndrome (ACS) is a leading cause of death in sickle cell disease (SCD). A suspicion of the presence or the development of ACS during a......READ MORE
Patients with sickle cell disease (SCD) are at risk for end-organ damage, including silent cerebral infarcts and associated cognitive deficits. Rou......READ MORE
