Results 31 to 40 of about 565 (123)

Abstract Book for the 27th Congress of the European Hematology Association

, 2022
HemaSphere, Volume 6, Issue S3, Page 1-4130, June 2022.
wiley   +1 more source

A Possible Case of β‐Thalassemia From the Cemetery of Santa Maria Maggiore in Vercelli (Piedmont, Northern Italy,18th Century)

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, C. Tesi, A. Mazzucchi, A. Vanni, M. Licata   +4 more
wiley   +1 more source

Thalassemia: essential radiographic and clinical features of interest to dentistry [PDF]

RGO: Revista Gaúcha de Odontologia, 2008
Thalassemia is a type of hereditary anemia that predominantly affects individuals born in or descendents of countries bathed by the Mediterranean Sea, such as Italy and Greece.
Luiz Roberto Coutinho Manhães Junior, Cláudio Costa, Marcelo Eduardo Pereira Dutra, Felipe Paes Varoli, Jefferson Xavier Oliveira   +4 more
doaj  

Talassemia e hanseniase

Hansenologia Internationalis, 1983
A talassemia β foi investigada em 165 brasileiros descendentes não miscigenados de italianos, 80 dos quais eram doentes de hanseníase, da forma virchowiana, e 85 estudantes universitários (grupo controle).
Antonio Sérgio RAMALHO, Walter PINTO JÚNIOR, Luis Alberto MAGNA, Bernardo BEIGUELMAN   +3 more
doaj   +1 more source

DIAGNÓSTICO MOLECULAR DE BETA TALASSEMIA INTERMÉDIA: RELATO DE HETEROZIGOTO COMPOSTO PARA MUTAÇÃO HBB:C.118C>T (CD39) E HBB:C.-138C>T (-88C>T)

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, ACM Berti, GA Bernardino, LA Souza-Junior, IS Dias, RD Costa, MF Galera, L Gazarini, E Belini-Júnior   +8 more
doaj   +1 more source

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

A importância do diagnóstico precoce na prevenção das anemias hereditárias The importance of early diagnosis in the prevention of hereditary anemias

Revista Brasileira de Hematologia e Hemoterapia, 2006
As anemias hereditárias, que englobam as hemoglobinopatias e talassemias são doenças determinadas geneticamente. Na maioria dos casos os heterozigotos são assintomáticos e desconhecem o defeito genético do qual são portadores.
Paulo R. Melo-Reis, Luiz M. M. Araújo, Karlla G. B. Dias-Penna, Mauro M. Mesquita, Frank S. Castro, Sérgio H. N. Costa   +5 more
doaj   +1 more source

EHA2021 Virtual Congress Abstract Book

, 2021
HemaSphere, Volume 5, Issue S2, June 2021.
wiley   +1 more source

Síndrome de Plummer-Vinson: uma rara associação na talassemia Plumer-Vinson syndrome: a rare association with thalassemia

Revista Brasileira de Hematologia e Hemoterapia, 2007
A síndrome de Plummer-Vinson é caracterizada por disfagia cervical, deficiência de ferro e presença de membrana esofágica. Neste estudo, relatam-se dois casos dessa síndrome em irmãos adolescentes.
Eduardo Crema, Ana Marcela R. Fonseca, Lara Beatriz P. Ribeiro, Cecília Aparecida D. Bello, Paulo Roberto J. Martins, Alex Augusto Silva   +5 more
doaj   +1 more source

Long‐term outcomes of avascular necrosis in sickle cell disease using joint‐specific patient‐reported outcome measures: Results from a multicentre study

British Journal of Haematology, Volume 206, Issue 1, Page 310-319, January 2025.
Summary Avascular necrosis (AVN) is a prevalent and progressive complication in young patients with sickle cell disease (SCD), but no study evaluated the long‐term subjective and objective outcome measures. Oxford hip score (OHS) and Oxford shoulder scores (OSS) are validated joint‐specific patient‐reported outcome measures (PROMs). In this prospective
Maddalena Casale, Giuseppe Toro, Federica Porcelli, Alessandra Quota, Rosamaria Rosso, Vincenzo Spadola, Francesco Arcioni, Saveria Campisi, Domenico Roberti, Silverio Perrotta   +9 more
wiley   +1 more source