Results 191 to 200 of about 88,496 (299)

New RHCE*cE allele with c.872C>G and variable RH3 and RH4 phenotypes, predicted to encode p.Pro291Arg

Transfusion, EarlyView.
Evelyne Heng, Gabriel Neto Braga, Marine Branger, Mylene Flammang, Christophe Tournamille, Aline Floch   +5 more
wiley   +1 more source

Rethinking Sickle Cell Disease as a Systemic Vasculopathy. [PDF]

Cells
DuPont M, Galadanci NA, Patel RV, Lebensburger J, Kanter J.   +4 more
europepmc   +1 more source

FIVE FACTS YOU SHOULD KNOW ABOUT SICKLE CELL DISEASE

A child gets sickle cell disease (SCD) when he or she receives two sickle cell genes\u2014one from each parent.SCD can be cured for certain patients.A child who inherits only one sickle cell gene has sickle cell trait (SCT).

core  

India's digital-first approach to sickle cell disease elimination. [PDF]

Arch Public Health
Nair AR.
europepmc   +1 more source

A Novel Plasma Heme Assay Reveals Disease Severity in Beta‐Thalassemia and Sickle Cell Anemia

American Journal of Hematology, Volume 101, Issue 7, Page 1706-1716, July 2026.
ABSTRACT Anemia results from imbalanced hemoglobin or red blood cell production and clearance. Hemolytic anemia, caused by premature red blood cell removal, can be intravascular (in blood) or extravascular (erythrophagocytosis). Hemolysis is common in Sickle Cell Disease (SCD) and Beta‐Thalassemia anemia (β‐thalassemia), the most prevalent inherited ...
Laurent Kiger, Nicolas Hebert, Laura Bencheikh, Vincent Malcor Deydier de Pierrefeu, Anne‐Laure Pham Hung d’Alexandry d’Orengiani, Sandia Adypagavane, Meghan Perkins, Laura Matabishi‐Bibi, France Pirenne, Claire Berquet, Stephane Moutereau, Serge Pissard, Frédéric Galactéros, Michael C. Marden, Pablo Bartolucci   +14 more
wiley   +1 more source

Sustainment of Hydroxyurea Adherence in Patients With Sickle Cell Disease.

JAMA Netw Open
Heitzer AM, Wooten Z, Luo G, Treadwell M, King AA, Gordeuk VR, Shah N, Abrams CM, McCuskee S, Gollan S, Longoria J, Hankins JS, Sickle Cell Disease Implementation Consortium.   +12 more
europepmc   +1 more source

The Role of Implicit Bias in Shaping Medication Prescribing Practices: A Scoping Review

JACCP: JOURNAL OF THE AMERICAN COLLEGE OF CLINICAL PHARMACY, Volume 9, Issue 7, July 2026.
ABSTRACT Background The most significant risk of implicit bias is that it is often unrecognized and unaddressed. Unidentified implicit bias in health care can hinder the appropriate prescribing of medications in underserved groups. This requires the strategic measurement of implicit bias to assess its impact, using methods such as the implicit ...
Angel M. Edwards, Olubukola A. Tikare, Noelia Dulo, Antoinette B. Coe, Steven R. Erickson, Michael P. Dorsch   +5 more
wiley   +1 more source

Co‐occurring opioid and stimulant use disorder and the relationship to severe maternal morbidity

Pregnancy, Volume 2, Issue 4, July 2026.
Abstract Introduction To evaluate the impact of the use of opioids, stimulants, or both on the rates of various severe maternal morbidity (SMM) events during inpatient delivery‐related hospitalizations among patients with substance use disorder (SUD).
Tucker E. Doiron, Noor Al‐Hammadi, Alexandra R. Schroeder, Niraj R. Chavan   +3 more
wiley   +1 more source

Eye problems and sickle cell trait : learn how you can help protect your vision [Spanish]

Eye problems and sickle cell trait : learn how you can help protect your vision [Spanish]FS_Glaucoma_LAY-es-508 ...

core  

Severe maternal morbidity according to sickle cell disease genotype

Pregnancy, Volume 2, Issue 4, July 2026.
Abstract Background Sickle cell disease (SCD) is a genetic hemoglobinopathy that disproportionately affects individuals of African descent and is associated with elevated risks of maternal complications. However, the contribution of specific SCD genotypes to severe maternal morbidity (SMM) and postpartum readmission remains poorly characterized at the ...
Tetsuya Kawakita, Natsume Furukawa, Sora A. Jones, Salimah Navaz Gangji   +3 more
wiley   +1 more source