نتایج جستجو برای: beta thalassemia

تعداد نتایج: 193529  

2017
Sandra Stella Lazarte María Eugenia Mónaco Magdalena María Terán Ana Cecilia Haro Miryam Emilse Ledesma Achem Blanca Alicia Issé

BACKGROUND Oxidative stress may aggravate symptoms of hemolytic anemias such as beta-thalassemia. FoxO3 activation results in resistance to oxidative stress in fibroblasts and neuronal cell cultures. OBJECTIVE The purpose of this research was to study FoxO3 gene expression and oxidative status in beta-thalassemia minor individuals. METHODS Sixty-three subjects (42 apparently healthy individ...

  Background :Highserum level of cancer antigen 15.3 (CA15.3) has been reported in some malignant and nonmalignant conditions including thalassemia major which could have been resulted from ineffective erythropoiesis. We aimed to evaluate the serum level of CA15.3 in carriers of beta-thalassemia by comparing them with cancer patients and healthy individuals.   Methods : This cross-sectional stu...

Journal: :Blood 1983
R Galanello R Ruggeri E Paglietti M Addis M A Melis A Cao

In this article we report a Sardinian family, in which a beta-thalassemia gene and a triple alpha-globin loci, counterpart of the rightward deletion type alpha-thalassemia-2, were segregating. The analysis of the genotype-phenotype correlations in the different family members allowed us to give an outline of the manifestations associated with different genotype combinations. The heterozygote fo...

2017
Afzal Shamsi Fardin Amiri Abbas Ebadi Musab Ghaderi

BACKGROUND Thalassemia major has become a public health problem worldwide, particularly in developing and poor countries, while the role of educating the family and community has not been considered enough in patients' care. OBJECTIVES This study examines the impact of partnership care model on mental health of patients with beta-thalassemia major. MATERIALS AND METHODS This experimental st...

Journal: :international journal of hematology-oncology and stem cell research 0
hamid choobineh department of medical laboratory sciences, faculty of para- medicine, tehran university of medical sciences sj dehghani department of medical laboratory sciences, faculty of para- medicine, tehran university of medical sciences shaban alizadeh department of hematology and blood banking, faculty of para- medicine, tehran university of medical sciences v ghobadi dana department of pediatrics, faculty of medicine, tehran university of medical sciences n saiepour department of biochemistry, faculty of medicine, tehran university of medical sciences r meshkani department of epidemiology and biostatistics, school of public health, tehran university of medical sciences

introduction: leptin is an adipocyte-derived hormone. exogenous leptin allows the recovery of the reproductive function. in humans, leptin correlates positively with the body mass index (bmi). the aim of this study was to investigate the association of leptin with the toxic effects of iron overload. methods: 219 major beta thalassemic patients (119 men, 100 women) and 137 non thalassemic indivi...

Journal: :iranian journal of pediatric hematology and oncology 0
i shahramian department of pediatric, zabol university of medical sciences, zabol, iran nm noori department of pediatric, children and adolescents health research center, zahedan university of medical sciences, zahedسازمان اصلی تایید شده: دانشگاه علوم پزشکی زابل (zabol university of medical sciences) a teimouri ahedan, iran 3. m.phil, phd in demography, children and adolescents health research center, zahedan university of medicaسازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) e akhlaghi general physician, faculty of medicine, zabol university of medical sciences, zabol, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی زاهدان (zahedan university of medical sciences) e sharafi resident of ophthalmology, zahedan university of medical sciences, zahedan, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی زابل (zabol university of medical sciences)

background polypeptide hormone leptin suppresses inflammation in the heart muscle and protects heart from diseases. the purpose of this study is to evaluate the relationship between leptin and troponin serum levels with cardiac involvement in patients with major beta thalassemia. materials and methods in this cross-sectional study, 70 children with major thalassemia were selected. two ml blood ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
Manuela Uda Renzo Galanello Serena Sanna Guillaume Lettre Vijay G Sankaran Weimin Chen Gianluca Usala Fabio Busonero Andrea Maschio Giuseppe Albai Maria Grazia Piras Natascia Sestu Sandra Lai Mariano Dei Antonella Mulas Laura Crisponi Silvia Naitza Isadora Asunis Manila Deiana Ramaiah Nagaraja Lucia Perseu Stefania Satta Maria Dolores Cipollina Carla Sollaino Paolo Moi Joel N Hirschhorn Stuart H Orkin Gonçalo R Abecasis David Schlessinger Antonio Cao

beta-Thalassemia and sickle cell disease both display a great deal of phenotypic heterogeneity, despite being generally thought of as simple Mendelian diseases. The reasons for this are not well understood, although the level of fetal hemoglobin (HbF) is one well characterized ameliorating factor in both of these conditions. To better understand the genetic basis of this heterogeneity, we carri...

2011
Isabela Sandrin Chinelato Gisele Cristine de Souza Carrocini Claudia Regina Bonini-Domingos

DOI: 10.5581/1516-8484.20110128 Thalassemias are common monogenic disorders caused by partial or complete reduction synthesis of one or more globin chains.(1) The normal concentrations of fetal hemoglobin (Hb F) in adults without Hb alterations range from 0% to 1%.(2) It is known that stimulation of Hb F production is beneficial to homozygous beta-thalassemia individuals(3) and that the XmnI po...

Journal: :Blood 1988
J M Gonzalez-Redondo T A Stoming K D Lanclos Y C Gu A Kutlar F Kutlar T Nakatsuji B Deng I S Han V C McKie

The presence of various substitutions and deletions resulting in beta-thalassemia was studied in 19 black patients with homozygous beta-thalassemia and in numerous relatives; all patients were from Georgia, South Carolina, and Alabama. Methodology included gene mapping, amplification of genomic DNA with Taq polymerase, identification of known nucleotide substitutions or a single nucleotide dele...

Journal: :Acta haematologica 2016
Taiwo R Kotila

BACKGROUND Sickle cell trait (SCT) is the heterozygous form of sickle cell disease and expectedly should be a benign state with no complications ascribed to it. There are numerous reports challenging its being a benign condition, though this is controversial. METHODS AND RESULTS A review of the results of the accompanying investigations done on some of the patients show that beta thalassemia ...

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