Results 111 to 120 of about 1,157,565 (202)

Evaluation of Discrimination Indices Validity for Screening of β-Thalassemia Trait

open access: yesMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, 2009
Background and Objectives: β-thalassemia trait (β-TT) and iron deficiency anemia (IDA) are the most common forms of microcytic anemia. Screening of β-thalassemia trait is important for medical counseling before marriage and preventing ...
A Ahmadi   +4 more
doaj  

The Post-Storage Performance of RBCs from Beta-Thalassemia Trait Donors Is Related to Their Storability Profile. [PDF]

open access: yesInt J Mol Sci, 2021
Anastasiadi AT   +13 more
europepmc   +1 more source

Evaluation of soluble transferring receptor levels in children with iron deficiency and beta thalassemia trait, and in newborns and their mothers

open access: yesThe Turkish Journal of Pediatrics, 2002
In this study we first aimed to investigate the value of soluble transferrin receptor levels (sTfR) in healthy, iron deficient and beta thalassemia trait children and to determine whether sTfR is a useful indicator of iron deficiency. Secondly, we
Aziz Polat   +3 more
doaj  

BETA-THALASSEMIA DUE TO A T-]A MUTATION WITHIN THE ATA BOX

open access: yes, 1988
Sequence analyses of amplified DNA from a Yugoslavian patient with Hb Lepore-.beta.-thalassemia and from his father with a simple .beta.-thalassemia trait have revealed a T .fwdarw.
STOMING, TA   +8 more
core   +1 more source

Recent trends in the gene therapy of β-thalassemia

open access: yes, 2015
Alessia Finotti,1–3 Laura Breda,4 Carsten W Lederer,6,7 Nicoletta Bianchi,1–3 Cristina Zuccato,1–3 Marina Kleanthous,6,7 Stefano Rivella,4,5 Roberto Gambari1–3 1Laboratory for the Development of Gene and Pharmacogenomic Therapy of
Gambari R   +7 more
core  

Frequency of beta-thalassemia trait in families of thalassemia major patients, Lahore.

open access: yesJournal of Ayub Medical College, Abbottabad : JAMC, 2014
Thalassemia major is one of the most common genetic disorders in Pakistan and over five thousand new patients are added in the pool annually. This familial disease has both medical and social implications, and therefore there is a need to assess the magnitude of beta-Thalassemia trait amongst family members of Thalassemia major patients.This cross ...
Tazeen, Majeed   +4 more
openaire   +1 more source

Beta thalassemia IVS-I-5(G-->C) heterozygosity masked by the presence of HbJ-Meerut in a Dutch-Indian patient

open access: yesHaematologica, 2006
We describe the genotype/phenotype correlation in a 35 year old anemic female referred to our laboratory because a fast eluting minor fraction on HPLC, mild hemolysis and hematological parameters suggesting a Thalassemia trait, eventually in combination ...
PC Giordano   +4 more
doaj  

Evaluation of physical growth of Patient WithThalassemia Major Based on NCHS criteria [PDF]

open access: yes
Background: Beta thalassemia major, including the conditions in which the natural growth due to complications from those diseases can be disrupted. Despite the recent advances in treating these patients, growth retardation in a significant percentage of ...
آریش, گیتی   +4 more
core  

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