Results 151 to 160 of about 41,952 (292)

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

Genetic variants in red blood cell adhesion-related genes influence the severity of sickle cell anemia in a malaria-endemic region : Short title: Genetic variants in red blood cell adhesion-related genes in sickle cell anemia. [PDF]

Mol Biol Rep
Matos I, Santos B, Gonçalves E, Lopes P, Brito M, Arez AP, Faustino P.   +6 more
europepmc   +1 more source

Providing space in genetic counseling: Reflexive thematic analysis of long and short sessions across clinical specialties

Journal of Genetic Counseling, Volume 35, Issue 3, June 2026.
Abstract The duration of genetic counseling (GC) sessions can vary significantly. However, which factors contribute to sessions being abbreviated or extended and how that affects quality of care has not been well studied. This study explored variability in long versus short GC patient care time, defined as time spent in the session with the patient ...
Emily Glanton, Deborah Cragun, Heather Zierhut   +2 more
wiley   +1 more source

Persistent Splenomegaly Is Associated with Morbidity in Tanzanian Children with Sickle Cell Anemia: Secondary Analysis of the SPHERE Trial. [PDF]

Acta Haematol
Ambrose EE, Tomlinson G, Ngoya PS, Stuber SE, Latham TS, Ware RE, Makubi AN, Smart LR.   +7 more
europepmc   +1 more source

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

Serum Vitamin A levels in children with sickle cell anemia: relationship with pulmonary function indices. [PDF]

BMC Pediatr
Ezenwosu OU, Chukwu BF, Ezenwosu IL, Mbah OK, Urom KO, Uwaezuoke NA, Nvene VO, Ikefuna AN, Emodi IJ.   +8 more
europepmc   +1 more source

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

3 Tips for Safe Use of Medicines for People with Sickle Cell Disease [French]

3 Tips for Safe Use of Medicines for People with Sickle Cell Disease [French]Les personnes atteintes de dr\ue9panocytose se voient souvent prescrire des m\ue9dicaments pour les complications fr\ue9quentes de la dr\ue9panocytose.CS 319852-MPublication ...

core  

Interview with Rudy Canzater - OH 321

, 1984
This collection includes an interview of Rudy S. Canzater (1939-2019) regarding the Dr. James R. Clark Memorial Sickle Cell Foundation. In her interview, Mrs. Canzater discusses her education, her personal connection to sickle cell anemia and Dr. Clark’s
Canzater, Rudy S., Sickle Cell Anemia Foundation   +1 more
core  

Primary and secondary stroke prophylaxis in children with sickle cell anemia: a meta-analysis. [PDF]

Blood Adv
Rangarajan HG, Mejias-Figueroa JA, Gehred A, Rodeghier M, DeBaun MR.   +4 more
europepmc   +1 more source