Results 151 to 160 of about 53,686 (285)
Study of Pregnancy Outcome in E-Beta Thalassaemia Mothers [PDF]
, 2009 Forty eight E-Beta thalassaemia patients were studied in NRS Medical College, Kolkata, West Bengal during the period from 2000-2006. In all patients Hb% ranged from 5.2g% - 9.6g%.
Bhattacharyaya, Maitryaee +1 more
core +1 more source
Lipid Nanoparticles for Delivery of CRISPR Gene Editing Components
Small Methods, Volume 10, Issue 2, 22 January 2026.The review presents a comprehensive overview of each component of lipid nanoparticles（LNPs）and their effects on editing efficiency. It specifically highlights strategies for achieving non‐liver delivery, aiming for broader applications in gene editing. Furthermore, this review summarizes the applications of LNPs in gene editing and offers insights for ...
Fan Wu +6 more
wiley +1 more source
Health Care Challenges of Hereditary Common Hematological Disorders in Odisha, India [PDF]
, 2012 Medical Genetics over the past few decades have emerged as an important and powerful medical specialty with increasing appreciation of its role and function in the biomedical sciences.
Balgir, RS
core +1 more source
Small Structures, Volume 7, Issue 1, January 2026.This work developed a PDC nanoplatform that orchestrated a multimodal synergistic therapy, combining active targeting, photothermal therapy, and iron nutrient deprivation. The antifungal, anti‐inflammatory efficacy and corneal repair ability of nanoplatform were demonstrated through both in vitro and in vivo evaluations.
Ruojiao Feng +13 more
wiley +1 more source
Therapeutic Value of Silymarin as Iron Chelator in Children with Beta Thalassemia with Iron Overload
Mediterranean Journal of Hematology and Infectious Diseases, 2014 Beta thalassemia is an inherited hemoglobin disorder resulting in chronic hemolytic anemia. The most common treatment for thalassemia is blood transfusion which is necessary to provide the patients with healthy red blood cells containing normal ...
adel abd elhaleim hagag
doaj
A rare case of gilberts syndrome with beta thalassemia trait in pregnancy [PDF]
Dr.Sruthi mandati, Dr.Sahitya bammidi
openalex +1 more source
Aging Cell, Volume 25, Issue 1, January 2026.Humanized mice offer new insight into immune‐hormonal changes during menopause. Traditional models lack accuracy in replicating human menopause physiology. Functional foods may ease symptoms but need testing in human‐relevant systems. Combining humanized mice with diet research can improve women's health outcomes.
Nisansala Chandimali +6 more
wiley +1 more source
Acta Obstetricia et Gynecologica Scandinavica, Volume 105, Issue 1, Page 30-49, January 2026.Rebiopsied and revitrified blastocysts may be linked to lower pregnancy and live birth rates in single euploid frozen embryo transfer cycles (very low‐quality evidence). Subgroup effects by biopsy day and morphology may hold clinical relevance and guide future study design.
Alessandra A. Vireque +4 more
wiley +1 more source
Khyber Medical University Journal, 2018 OBJECTIVE: To determine the frequency of beta thalassemia trait in pregnant anemic patients attending Khyber Teaching Hospital, Peshawar, Pakistan. METHODS: This descriptive cross sectional study was conducted in Gynecology and Obstetrics Department of ...
Maimoona Qadir, Sohail Amir
doaj
British Journal of Haematology, Volume 208, Issue 1, Page 367-372, January 2026.Opposite to the age trend in healthy children, cerebral blood flow increases with age in children with sickle cell anaemia. Early treatment with hydroxyurea (hydroxycarbamide) may help slow this abnormal trend and protect brain functions.
Ping Zou Stinnett +10 more
wiley +1 more source