Results 21 to 30 of about 1,548 (194)
TALASSEMIA: REVISÃO DE LITERATURA E AVANÇOS NO TRATAMENTO DA BETA TALASSEMIA
E.Y.K. Ueda +7 more
doaj +2 more sources
JORNADA DO PACIENTE COM TALASSEMIA BETA NO BRASIL: PERCEPÇÕES DO TRATAMENTO
Introdução/Objetivos: A talassemia é um tipo de anemia hereditária que faz parte de um grupo de doenças do sangue chamadas hemoglobinopatias. A jornada do paciente envolve diversas etapas e mapear sua experiência é fundamental para encontrar formas de ...
ABM Almeida +5 more
doaj +1 more source
5613417 CO-TREATMENT OF ERYTHROID CELLS ISOLATED FROM Β039-THALASSEMIA PATIENTS WITH CRISPR-CAS9 GENE EDITING AND FETAL HEMOGLOBIN INDUCTION [PDF]
HemaSphere, Volume 7, Issue S1, Page 41-41, April 2023.
M.L.P. Lipucci di Paola +5 more
europepmc +2 more sources
5613423 TREATMENT OF ERYTHROID PRECURSOR CELLS FROM β-THALASSEMIC PATIENTS WITH ISOXAZOLE DERIVATIVES: POTENT INDUCTION OF FETAL HEMOGLOBIN [PDF]
HemaSphere, Volume 7, Issue S1, Page 17-17, April 2023.
C.Z. Cristina Zuccato +9 more
europepmc +2 more sources
Abstract Although numerous patient‐specific co‐factors have been shown to be associated with worse outcomes in COVID‐19, the prognostic value of thalassaemic syndromes in COVID‐19 patients remains poorly understood. We studied the outcomes of 137 COVID‐19 patients with a history of transfusion‐dependent thalassaemia (TDT) and transfusion independent ...
Ibrahim El‐Battrawy +49 more
wiley +1 more source
Il racconto della talassemia: Nelle mie vene e Paura di guarire
Il presente studio intende analizzare il racconto della talassemia in due testi contemporanei: Paura di guarire, di Ivano Argiolas (2021), e Nelle mie vene, di Flavio Soriga (2019).
Ramona Onnis
doaj +1 more source
PROTOCOLOS CLÍNICOS EM BETA-TALASSEMIA
Objetivos: Este trabalho tem como objetivo realizar um levantamento estatístico sobre os principais protocolos de pesquisa clínica, utilizando o banco de dados do Clinical Trials, envolvendo terapia gênica em pacientes com beta-talassemia. Pacientes portadores de talassemias, principalmente com o quadro de beta-talassemia major, sofrem de uma ...
LAB Faria, FM Lima, JVDS Bianchi
openaire +2 more sources
Abstract Background The average hemoglobin content of red cell concentrates (RCC) varies depending on the method of preparation. Surprisingly less data are available concerning the clinical impact of those differences. Study Design and Methods The effects of two types of RCC (RCC‐A, RCC‐B) on transfusion regime were compared in a non‐blinded ...
Maria Rita Gamberini +15 more
wiley +1 more source
P129: NARRATING SICKLE CELL DISEASE: THE EXPERIENCES OF PATIENTS AND CARGIVERS [PDF]
HemaSphere, Volume 6, Issue S1, Page 32-32, January 2022.
De Franceschi L +13 more
europepmc +2 more sources
Selecting β‐thalassemia Patients for Gene Therapy: A Decision‐making Algorithm
This expert opinion originally developed by a panel of the Italian Society of Thalassemias and Hemoglobinopathies (SITE), reviewed and adopted by the European Hematology Association (EHA) through the EHA Scientific Working Group on Red Cells and Iron, has been developed as priority decision‐making algorithm on evidence and consensus with the aim to ...
Donatella Baronciani +13 more
wiley +1 more source

