Results 151 to 160 of about 29,542 (277)

G‐CSF for Mobilizing CD34+ Cells in Individuals With SCD: A Word of Caution

American Journal of Hematology, Volume 101, Issue 6, Page 1178-1181, June 2026.
Akshay Sharma, Allistair Abraham, Monica Bhatia, María Cancio, Sonali Chaudhury, Selim Corbacioglu, Gregory M. T. Guilcher, Ashish O. Gupta, Rabi Hanna, Matthew M. Heeney, Tami John, Lakshmanan Krishnamurti, James L. LaBelle, Hemalatha G. Rangarajan, Shalini Shenoy, Elizabeth Stenger, Crawford Strunk, Courtney D. Fitzhugh   +17 more
wiley   +1 more source

Hemoglobin Sickle-Beta-Thalassemia With an Acute Crisis. [PDF]

Cureus
Tokuno H, Ishizuka K, Seki T, Kosaka S.
europepmc   +1 more source

Variation in Chronic Automated Red Cell Exchange Practices for Sickle Cell Disease: Insights Into Isovolemic Hemodilution Use

Journal of Clinical Apheresis, Volume 41, Issue 3, June 2026.
ABSTRACT Prior surveys of chronic automated red blood cell exchange (RCE) for patients with sickle cell disease (SCD) have identified considerable procedural variability, especially with the use of isovolemic hemodilution red blood cell exchange (IHD‐RCE).
Jennifer M. Jones, Fatima Aldarweesh, Nicole Aqui, Aleh Bobr, Patricia Brunker, Mischa L. Covington, Juliana Guarente, Robert Hagar, Matthew Karafin, Divjot Singh Lamba, Grace Lee, Wen Lu, Ethan A. Mack, Gagan Muthur, Saadiya Nazli, Halima Olaniyan, Chinelo P. Onyenekwu, Jay S. Raval, Divya Setya, Yvette C. Tanhehco, Mamie Thant, Angelica Vivero, Yanyun Wu, Edward C. C. Wong, Nalan Yurtsever, Yan Zheng, Patricia A. Shi, Jennifer Webb   +27 more
wiley   +1 more source

Detecting sickle hemoglobin. [PDF]

BMJ, 1972
openaire   +2 more sources

Development of a Clinical Severity Score for Indian Sickle Cell Anaemia Patients

eJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Background Sickle cell anaemia (SCA) is a monogenic disorder but shows variable disease severity. We evaluated the utility of paediatric severity scores (PSS) in Indian patients and developed two modified scores: Indian Severity Score 1 (ISS1) by adding four clinical parameters to PSS, and ISS2 by excluding four biochemical measures from ISS1.
Suraj S. Nongmaithem, Amitabh Biswas, Swaroop Iyer, Jandhayala Vyshnavi, Archana Wath, Giriraj R. Chandak, Dipty Jain   +6 more
wiley   +1 more source

International flight-associated splenic infarction in a 33-year-old man with sickle cell trait. [PDF]

CMAJ
Chadelat A, Tassart M, Bachmeyer C.
europepmc   +1 more source

What you should know about diabetes tests if you have sickle cell trait [PDF]

If you have sickle cell trait (SCT), the hemoglobin A1C test used to test and monitor diabetes (a potentially lifelong disease in which you have high levels of sugar in your blood) may give false results which can affect the care you receive from your ...

core  

Prevalence of Low Bone Mineral Density Increases With Age in Sickle Cell Disease

eJHaem, Volume 7, Issue 3, June 2026.
ABSTRACT Introduction Skeletal complications are common in sickle cell disease (SCD). We previously showed that the prevalence of low areal bone mineral density (aBMD) increased with age in a pediatric SCD cohort, even after adjusting for short stature. Data on age‐related aBMD trends in young adults is lacking.
Jahnavi Gollamudi, Chengzhou Wu, Guolian Kang, Michael Sexton Lamonica, Pei‐Lin Chen, Ragha Srinivasan, Khalid El‐Bashir, Jane Hankins, Parul Rai, Clifford Takemoto, Hyacinth I. Hyacinth, Matthew R. Allen, Babette S. Zemel, Oyebimpe Adesina   +13 more
wiley   +1 more source

Lights, camera, occlusion! watch sickle cells in real time. [PDF]

Blood Adv
Gurkan UA.
europepmc   +1 more source

Suzetrigine for Vaso-Occlusive Pain in Sickle Cell Disease: A Three-Patient Case Series. [PDF]

Orthop Rev (Pavia)
Joudeh S, Moore D, Hasoon J, Robinson CL, Idowu M, Oso T.   +5 more
europepmc   +1 more source