نتایج جستجو برای: b thalassemia

تعداد نتایج: 917848  

Journal: :Haematologica 2001
J Traeger-Synodinos I Papassotiriou C Vrettou C Skarmoutsou A Stamoulakatou E Kanavakis

BACKGROUND AND OBJECTIVES The degree of globin chain imbalance and tissue hypoxia are important determinants of clinical severity in thalassemia syndromes. Thus phenotypic expression may be modified by interaction of alpha- and beta-thalassemia defects, level and type of hemoglobin synthesized and oxygen release to the tissues. We evaluated hematology, erythroid marrow activity and functional a...

M. Zeinali S. Delmaghani S. Zeinali Z. Azizi, Z. Moghaddam

Background: It is estimated that about 3,000 pregnancies in Iran are at risk for b-thalassemia each year. Objective: To evaluate the diagnostic accuracy of combination of ARMS/PCR and  RFLP/PCR techniques in prenatal diagnosis of b-thalassemia.Methods: Sixty-seven b-thalassemia carrier families were enrolled in this study. To analyze b-globin gene, amplification refractory mutation system (ARMS...

2015
Umar Saeed Yasir Waheed Muhammad Ashraf Usman Waheed Sadia Anjum Muhammad Sohail Afzal

Hepatitis B and C are serious public health problems worldwide. Thalassemia patients are dependent on blood transfusions throughout their life and are at high risk of viral infections. The aim of this study was to estimate the prevalence of hepatitis B/C infections and different clinical parameters in multitransfused thalassemia population. In this study, 262 multitransfused β-thalassemia patie...

Journal: :Pakistan Armed Forces Medical Journal 2022

Objectives: To assess the immunogenicity of Hepatitis B Vaccine in children with thalassemia.
 Study Design: Prospective longitudinal study.
 Place and Duration Study: Pak Emirates Military Hospital, Rawalpindi Pakistan from Aug 2018 to Jan 2019.
 Methodology: After ethical approval informed consent, 150 diagnosed patients thalassemia were selected Thalassemia centre at Hospital ...

2011
Antonio Cao Paolo Moi Renzo Galanello

β-thalassemias are heterogeneous hereditary anemias characterized by a reduced output of β-globin chains. The disease is most frequent in the temperate regions of the world, where it represents an important health problem. In the last decades, several programs, aimed at controlling the birth rate of thalassemia newborns by screening and prenatal diagnosis of populations with high risk of β-thal...

Journal: :Blood 2010
Vito Di Marco Marcello Capra Emanuele Angelucci Caterina Borgna-Pignatti Paul Telfer Paul Harmatz Antonis Kattamis Luciano Prossamariti Aldo Filosa Deborah Rund Maria Rita Gamberini Paolo Cianciulli Marianne De Montalembert Francesco Gagliardotto Graham Foster Jean Didier Grangè Filippo Cassarà Angela Iacono Maria Domenica Cappellini Gary M Brittenham Daniele Prati Antonello Pietrangelo Antonio Craxì Aurelio Maggio

Chelation therapy with new drugs prevents cardiac damage and improves the survival of thalassemia patients. Liver diseases have emerged as a critical clinical issue. Chronic liver diseases play an important role in the prognosis of thalassemia patients because of the high frequency of viral infections and important role of the liver in regulating iron metabolism. Accurate assessment of liver ir...

2010
Spyridon Gorezis Ioannis Asproudis Nikolaos Chalasios Aikaterini Karali Elena Tsanou Dimitrios Peschos Aikaterini Christodoulou Miltiadis Aspiotis

PURPOSE Evaluation of contrast sensitivity in patients with beta-thalassemia major and sickle cell disease which undergo regular transfusions and chelation therapy with desferrioxamine (DFX). MATERIALS AND METHODS We studied contrast sensitivity in 48 eyes (24 patients) with beta-thalassemia major (group A) and in 42 eyes (21 patients) with sickle cell disease (group B), compared to 60 eyes o...

2014
N Honar S Kamali M Karimi

BACKGROUND We aimed to investigate the frequency of celiac disease in children with β-thalassemia major (B-TM) in Shiraz, southern Iran. MATERIALS AND METHODS In this study, the prevalence of celiac disease in children with B-TM was evaluated. Children with B-TM were screened for celiac disease by ant-tissue transglutaminase (anti-tTG) IgA antibody, IgA level and anti-tTG IgG. A total of 1500...

Journal: :Clinical chemistry 2005
Srinivas B Narayan Richard L Boriack Bette Messmer Michael J Bennett

References 1. Weatherall DJ. The thalassemias. In: Stamatoyannopoulos G, Majerus PW, Perlmutter RM, Varmus H, eds. The molecular basis of blood diseases, Vol. 3. Philadelphia: WB Saunders, 2001:183–226. 2. Chui DH, Fucharoen S, Chan V. Hemoglobin H disease: not necessarily a benign disorder. Blood 2003;101:791–800. 3. Lemmens-Zygulska M, Eigel A, Helbig B, Sanguansermsri T, Horst J, Flatz G. Pr...

Journal: :The Southeast Asian journal of tropical medicine and public health 2012
Siriyupa Sananreangsak Punyarat Lapvongwatanal Kamonmarn Virutsetazin Paranee Vatanasomboon Nan Gaylord

Children with thalassemia can thrive with quality care by their families. The purpose of this study was to examine predictors of family care behavior by family caregivers of children with thalassemia. Eighty-eight family caregivers for children with thalassemia aged 1-16 years were recruited by purposive sampling from in-patient and out-patient clinics in an eastern regional hospital in Thailan...

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