Results 121 to 130 of about 5,070,713 (217)
Evaluating Reproductive Health Recommendations in CPGs for Sickle Cell Disease: An Umbrella Review
Clinical and Public Health Guidelines, Volume 3, Issue 4, October 2026.ABSTRACT Background Individuals with sickle cell disease or trait (SCD/T) face significant reproductive health risks, highlighting the need to assess the best available evidence on their reproductive health needs. Objectives To assess the quality of SCD/T clinical practice guidelines and evaluate the key characteristics and quality of their ...
Lisa R. Roberts +4 more
wiley +1 more source
Three Tips for Safe Use of Medicines for People with Sickle Cell Disease
People with sickle cell disease (SCD) are often prescribed medicines for common complications of SCD.CS 319852-APublication date from document properties.sickle-cell-3-tips-safe-med-use-h ...
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Health Science Reports, Volume 9, Issue 10, October 2026.ABSTRACT Background Sickle cell anemia (SCA) may influence malaria susceptibility and clinical outcomes in endemic regions. However, the interaction between hemoglobin genotypes and malaria severity remain poorly defined in endemic African settings, particulary in Angola, where SCA and malaria impose a substantial public health burden.
Cruz S. Sebastião +3 more
wiley +1 more source
Steps to Better Kidney Health for People with Sickle Cell Disease [PDF]
People with sickle cell disease (SCD) are at greater risk than the general population for kidney complications. Share your medical history with your healthcare team so it can properly identify and treat any complications of SCD you currently have or may ...
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eJHaem, Volume 7, Issue 5, October 2026.ABSTRACT Introduction Automated erythrocytapheresis (aEEX) is an effective therapy for severe sickle cell disease (SCD). Its use in paediatrics can be limited by challenges in obtaining reliable venous access. Methods We conducted a retrospective, single‐centre study to evaluate the safety and feasibility of ultrasound (US)‐guided peripheral venous ...
Laura Ocello +12 more
wiley +1 more source
Ovarian Reserve in Women of Reproductive Age With Sickle Cell Anaemia: A Scoping Review
eJHaem, Volume 7, Issue 5, October 2026.ABSTRACT Background Sickle cell anaemia (SCA) is an inherited haemoglobinopathy disproportionately common among people of African origin, though it affects multiple global populations. Emerging evidence suggests that chronic haemolysis, inflammation and treatment exposures in SCA may affect ovarian function.
Kehinde Awodele +4 more
wiley +1 more source
Mission: To improve quality of life, life expectancy, and health among people living with sickle cell disease (SCD)
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eJHaem, Volume 7, Issue 5, October 2026.ABSTRACT Umbilical cord blood transplantation is a viable source of stem cells due to accessibility and low incidence of chronic graft‐versus‐host disease despite human‐leukocyte‐antigen mismatching. Disadvantages of low stem cell dose in larger recipients include delayed immune reconstitution, graft rejection, and mortality.
Rachel E. Granberg +4 more
wiley +1 more source
Mission: To improve quality of life, life expectancy, and health among people living with sickle cell disease (SCD)
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Iron and Other Metal Ions in Human Health and Disease
MedComm, Volume 7, Issue 10, October 2026.Iron, copper, zinc, and calcium orchestrate cellular function through distinct yet cooperative mechanisms: redox‐active iron and copper cycle between oxidation states to act as Fenton catalysts and electron carriers in oxidative phosphorylation (OXPHOS); redox‐inert zinc serves as a structural component of zinc‐finger proteins and a catalytic cofactor ...
Xiaofeng Dai, Jitian Li
wiley +1 more source