Results 91 to 100 of about 5,241 (198)
MicrobiologyOpen, Volume 15, Issue 5, October 2026.Green‐synthesized silver nanoparticles from Nepeta pogonosperma and Astrodaucus persicus significantly inhibit biofilm formation and downregulate bap gene expression in multidrug‐resistant clinical isolates of Acinetobacter baumannii. This eco‐friendly approach offers a promising strategy to combat antimicrobial resistance.
Maedeh Kakavan +6 more
wiley +1 more source
Heart failure in haemoglobinopathies: pathophysiology, clinical phenotypes, and management
, 2017 Hereditary haemoglobinopathies, mainly beta-thalassemia and sickle cell disease, constitute the most common monogenic disorders in humans, and although once geographically confined, they are currently globally distributed.
Parissis, J. +3 more
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3rd Pan-European Conference on Haemoglobinopathies and Rare Anaemias, 24-26 October 2012, Limassol - Cyprus [PDF]
, 2012 This abstract book contains all abstracts presented to the 3rd Pan-European Conference on Haemoglobinopathies and Rare Anaemias, 24-26 October 2012, Limassol ...
Christos Kattamis +4 more
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Acta Paediatrica, Volume 115, Issue 10, Page 2332-2340, October 2026.ABSTRACT Aim Childhood ischemic stroke is rare but causes substantial long‐term morbidity, and its heterogeneous aetiology complicates timely diagnosis and management. Methods We conducted a retrospective population‐based observational study using hospital data and chart review to describe diagnostics, treatment and outcomes of ischemic stroke in ...
Jussi V. Leinonen +8 more
wiley +1 more source
European Journal of Haematology, Volume 117, Issue 4, Page 943-952, October 2026.ABSTRACT Third allogeneic hematopoietic stem cell transplantation (HSCT3) is rarely performed in pediatric patients and is associated with high toxicity and mortality. Data on outcomes in this setting remain scarce. We conducted a retrospective multicenter study within the Spanish GETH‐TC Pediatric group including 29 children and adolescents who ...
Luisa Sisinni +17 more
wiley +1 more source
FREQUENCY OF BETA THALASSEMIA TRAIT AMONG THE HEALTHY INDIVIDUALS - A SINGLE CENTRE STUDY
Pakistan Armed Forces Medical Journal, 2018 Objective: To determine the frequency of beta thalassemia trait among the asymptomatic healthy individuals. Study Design: Cross sectional study. Place and Duration of Study: This was carried out at Pakistan Air Force (PAF) Hospital Lahore from ...
Muhammad Arif Sadiq +3 more
doaj
European Journal of Haematology, Volume 117, Issue 4, Page 1052-1060, October 2026.ABSTRACT Background Sickle cell disease (SCD) is a chronic and life‐limiting hemoglobin and systemic vascular disease. While over 1000 people have undergone hematopoietic cell transplantation (HCT) over the last 40 years, long‐term disease‐specific and health‐related quality of life data are lacking.
Gregory M. T. Guilcher +20 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 9, September 2026.ABSTRACT A 67‐year‐old man with decades of untreated sickle cell disease developed septic shock with multiorgan failure, splenic infarction, and marrow fibrosis; his genotype could not be confirmed. He recovered with intensive supportive care, with hydroxyurea initiated for long‐term disease modification, illustrating catastrophic infection‐triggered ...
Sara Shahidi, Gisha Mohan
wiley +1 more source
SKELETAL CHANGES IN THE HAEMOGLOBINOPATHIES
, 1966 1. Bone changes in the haemoglobinopathies are caused by either (a) chronic haemolysis with marrow hyperplasia, or (b) infarction, when Hb S is present in the red cells in amounts sufficient to allow sickling (and therefore vascular occlusion) in vivo.
A. B. Raper, J. H. Middlemiss
core +1 more source