Results 141 to 150 of about 18,864 (254)

Decoding thalassemia and sickle cell disease: advances in molecular technologies for comprehensive variant detection. [PDF]

Front Genet
Foord E, Sairafi D, Berg M, Westerling S, Adigun T, Uzunel M, Papasavva T, Uhlin M.   +7 more
europepmc   +1 more source

Plenary Abstracts Session & Oral Presentations

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Comprehensive Review of Genetic and Epigenetic Regulation of Fetal Hemoglobin in β-Hemoglobinopathies: From Molecular Mechanisms to Clinical Applications. [PDF]

Mediterr J Hematol Infect Dis
Abu Za'ror YSM, Suleiman JB, Delmani FA, Alhmoud JF, Ayasreh AM, Al-Wendawi SI, AlRamadneh TN, Azlan M.   +7 more
europepmc   +1 more source

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +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

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Beyond Iron Deficiency: An Atypical Peripheral Smear Revealing Hemoglobin C in an Adolescent. [PDF]

Cureus
Hamidine M, Awati M, Mehdi A.
europepmc   +1 more source

Health literacy and prenatal screening acceptability for hemoglobinopathies in Tunisia: a pilot mediation study. [PDF]

J Community Genet
Maaoui F, Saad NB, Zarrouk E, Mahjoub S, Menif S, Moumni I.   +5 more
europepmc   +1 more source

Clinical Trial Landscape of Gene-Edited Autologous Hematopoietic Stem Cells for Hemoglobinopathies and Immunodeficiencies. [PDF]

Int J Mol Sci
O'Hanlon Cohrt K, O'Dea S.
europepmc   +1 more source

Coinheritance of non‐deletional hemoglobin H disease with sickle cell trait

eJHaem
Veroniki Komninaka, Evangelia‐Eleni Ntelaki   +1 more
doaj   +1 more source