Results 41 to 50 of about 3,173 (204)
International Journal of Osteoarchaeology, Volume 35, Issue 5, Page 341-350, September/October 2025.ABSTRACT In Italy's Piedmont region, the city of Vercelli has a history of malaria transmission due to favorable conditions for Anopheles mosquitoes, which may have influenced the genetic prevalence of thalassemia. This study investigates the skeletal remains of a nonadult individual from the Church of Santa Maria Maggiore in Vercelli, dating to the ...
R. Fusco +4 more
wiley +1 more source
Microcytic anemia factor no estudo das anemias microcíticas [PDF]
, 2010 A anemia ferropénica e a β-Talassemia menor são as anemias microcíticas mais frequentes na prática laboratorial, sendo o seu diagnóstico de extrema importância clínica.
Barros, Clara, Teixeira, Joana
core
Determinação da sobrecarga de ferro na talassemia pela IRM hepática e ferritina [PDF]
, 2008 Accumulation of iron in thalassemia causes organ damage and reduces patient survival due to heart lesions in the second decade of life. Iron deposits are monitored by direct (biopsy) and indirect methods (ferritin) with sequential data being better than ...
ANGULO, Ivan L. +5 more
core +2 more sources
Abstract Book for the 2nd Sickle Cell & Thalassaemia Virtual Conference
, 2022 HemaSphere, Volume 6, Issue S1, Page 1-43, January 2022.
wiley +1 more source
Hematology, Transfusion and Cell TherapyObjetivo: Desenvolver modelo preditivo, usando a concentração da Hb S, como ferramenta de diagnóstico de alfa talassemia em portadores de traço falciforme. Metodologia: Foram analisados 241 indivíduos adultos com traço falciforme.
JPS Jaschke +5 more
doaj +1 more source
Hematology, Transfusion and Cell Therapy, 2023 Objetivo: Demonstrar a relevância do diagnóstico molecular na identificação de heterozigoto composto para beta talassemias HBB:c.118C>T (CD39) e HBB:c.-138C>T (-88C>T) em recém-nascido da triagem neonatal.
VS Ramos +8 more
doaj +1 more source
Le Basi biochimiche e molecolari delle talassemie e la diagnosi dell'Alfa-talassemia eterozigote [PDF]
, 1982 Recent aspects of molecular and biochemical basis of thalassemic syndromes are described together with laboratory methods suitable for diagnosis and screening of heterozygous α ...
Masala, Bruno Lucio
core
EHA2021 Virtual Congress Abstract Book
, 2021 HemaSphere, Volume 5, Issue S2, June 2021.
wiley +1 more source
HemaSphere, Volume 3, Issue S1, Page 23-24, June 2019., 2019 Background: While the efficacy and safety of deferiprone (DFP) in adult patients with transfusion‐dependent hemoglobinopathies (TDH) has been extensively studied, data in children are sparse. Aims: We report results of DEferiprone Evaluation in Pediatrics‐2 (DEEP‐2), (EudraCT Number 2012‐000353‐31), a Phase III multicentre, randomized, open label study
A. Kattamis +23 more
wiley +1 more source
Clinical and laboratorial diversity in the bantu haplotype of sickle cell anemia [PDF]
, 2006 Several factors have been identified as possibly being responsible for the diversity of sickle cell anemia patients symptoms, including gender, age, haplotypes and hemoglobin F levels.
Cipolotti, Rosana +3 more
core +3 more sources