Results 161 to 170 of about 88,496 (299)

USE OF OPIOIDS AND BURDEN OF DISEASE IN PATIENTS (PTS) WITH SICKLE CELL DISEASE (SCD) IN BRAZIL VS THE OVERALL POPULATION OF THE INTERNATIONAL SICKLE CELL WORLD ASSESSMENT SURVEY (SWAY)

Hematology, Transfusion and Cell Therapy, 2020
M. Pita, J. James, S. Forny, N. Ramscar, I. Osunkwo   +4 more
doaj   +1 more source

A rare presentation of hypersplenism in an adult female with homozygous sickle cell disease. [PDF]

J Surg Case Rep
Chhetri PK, Paudel P, Jha R, Prasad R, Agrawal S.   +4 more
europepmc   +1 more source

The Bloodline newsletter : Sickle Cell Data Collection (SCDC) Program quarterly newsletter ; Summer 2020

Mission: To improve quality of life, life expectancy, and health among people living with sickle cell disease (SCD)

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Sickle cell trait and splenic infarct : information for healthcare providers [PDF]

People with sickle cell trait (SCT) are generally healthy, but may develop splenic infarct.Healthcare providers can educate people about this complication of SCT, including raising awareness of the risks, signs and symptoms, as well as steps they can ...

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Transformed but Not Cured: The Ethics of Describing Gene-Editing Therapy for Sickle Cell Disease. [PDF]

Hastings Cent Rep
Wiggleton-Little J, Thomas SP, Walters K, Albright C.   +3 more
europepmc   +1 more source

The Bloodline newsletter : Sickle Cell Data Collection (SCDC) Program quarterly newsletter ; Winter 2021

Mission: To improve quality of life, life expectancy, and health among people living with sickle cell disease (SCD)

core  

Pediatric transfusion camp: Developing, piloting and evaluation of a Canadian national pediatric transfusion medicine curriculum

Transfusion, EarlyView.
Abstract Background Standardized post‐graduate education in pediatric transfusion medicine remains limited. The objective of this study was to adapt an adult transfusion education program, Transfusion Camp, to include pediatric content and assess knowledge improvement in pediatric subspecialty trainees.
Ines Zuna, Valérie Arsenault, Kimmo Murto, Suzanne Beno, MacGregor Steele, Jennifer Young, Sarah Leir, Angela Punnett, Cheryl Peters, Lucille Barcat, Yulia Lin, Casey Kapitany, Sophie Chargé, Teresa Skelton, Lani Lieberman   +14 more
wiley   +1 more source

CRISPR and Fanzor in sickle cell disease: current progress and future prospects. [PDF]

Front Genome Ed
Alhumoudi AY, Alotaibi AG, Alosaimi NF, Alshalani A, Alqahtani SM, Alsaab SM, Almutiri BJ, Albariqi MMH.   +7 more
europepmc   +1 more source

The Bloodline newsletter : Sickle Cell Data Collection (SCDC) Program quarterly newsletter ; Winter 2020

Mission: To improve quality of life, life expectancy, and health among people living with sickle cell disease (SCD)

core  

What you should know about sickle cell disease and pregnancy [PDF]

Sickle cell disease (SCD) is a genetic condition that is present at birth. It is inherited when a child receives two sickle cell genes\ue2\u20ac\u201done from each parent. A person with SCD can pass the disease on to his or her children.Sickle cell trait

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