Results 71 to 80 of about 21,024 (196)
Armaghane Danesh Bimonthly Journal, 2022 Background & aim: Beta thalassemia is one of the most common hereditary diseases in Iran. The birth of a child with thalassemia causes many social and economic problems for parents and the health care system.
E Shams +3 more
doaj
Health Screening and Post‐Arrival Services for Refugee Children From Afghanistan
Journal of Paediatrics and Child Health, EarlyView.ABSTRACT Aim To examine refugee health screening and services for Afghan children in the unique context of emergency expedited humanitarian resettlement in Melbourne, Australia. Methods Retrospective audit of Afghan children who attended a specialist child refugee health service between August 2021–April 2024. Results Participants included 218 children
Amy Williamson +5 more
wiley +1 more source
Arthritis in beta‐thalassemia minor [PDF]
Arthritis & Rheumatism, 1983 L, Górriz +3 more
openaire +2 more sources
Transfusion Medicine, EarlyView.Abstract Objective This study aimed to analyse the distribution and demand patterns of antigen‐negative red blood cells (RBCs) in Shandong Province, China (2022–2024), with a focus on ABO blood groups and clinically significant antigens. The research was designed to provide rigorous data for advancing precision transfusion protocols and to establish a ...
Aiping Zhao +7 more
wiley +1 more source
A global survey of blood transfusion practices for patients with sickle cell disease
Transfusion, EarlyView.Abstract Background Sickle cell disease (SCD) affects over 7 million people globally, with blood transfusion remaining a cornerstone of management. However, contemporary transfusion practices across diverse settings remain poorly characterized. We evaluated global transfusion practices for patients with SCD to identify gaps and inform resource ...
Jeremy W. Jacobs +18 more
wiley +1 more source
Renal tubular dysfunction with nephrocalcinosis in a patient with beta thalassemia minor
Saudi Journal of Kidney Diseases and Transplantation, 2008 Thalassemia is a hereditary anemia resulting from defect in hemoglobin production. Beta thalassemia is due to impaired production of beta globin chains, leading to a relative excess of alpha globin chains.
Prabahar Murugesan +4 more
doaj
Causes of New Cases of Major Thalassemia in Sistan and Balouchistan Province in South-East of Iran
Iranian Journal of Public Health, 2012 Background: Thalassemia is the most common monogenic disease in South-East of Iran. Despite the 70% reduction in Iranian thalassemia cases after thalassemia control comprehensive program, 601 affected babies were born in Sistan and Balouchistan Province,
S Izadi +3 more
doaj +2 more sources
Bioscientific Review, 2023 Objective The objective of this study was to study relation of ß-thalassemia and its types (major, minor, intermedia) with ABO and Rh blood groups in Lahore, Pakistan.
Kainat Waheed +2 more
doaj
American Journal of Hematology, Volume 101, Issue 9, Page 2297-2310, September 2026.ABSTRACT Hydroxyurea (HU) is the most widely prescribed disease‐modifying treatment in sickle cell disease (SCD), though treatment responses vary due to metabolism and adherence. We examined HU blood levels and treatment response in patients with homozygous sickle cell disease (HbSS).
Sigrid van der Veen +26 more
wiley +1 more source
Molecular Oncology, Volume 20, Issue 8, Page 1933-1962, August 2026.Glioma cells mainly express the endothelin receptor EDNRB, while EDNRA is restricted to a perivascular tumor subpopulation. Endothelin signaling reduces glioma cell proliferation while promoting migration and a proneural‐to‐mesenchymal transition associated with poor prognosis. This pathway activates Ca2+, K+, ERK, and STAT3 signalings and is regulated
Donovan Pineau +36 more
wiley +1 more source