نتایج جستجو برای: thalassemic patients

تعداد نتایج: 2085514  

2013
Faiez N. Hattab

OBJECTIVES To provide a description of mesiodistal crown diameters (MD) and tooth-size discrepancy (TSD) of the permanent dentition in patients with thalassemia major (TM) and to compare the results with those of unaffected control group. STUDY DESIGN The sample consisted of 46 thalassemic patients, 25 males and 21 females aged 7.3 to 23.7 years (mean ± SD = 11.2 ± 3.9 years) and control grou...

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...

2014
Gissou Hatami Niloofar Motamed

BACKGROUND Beta thalassemia major has a considerable impact on quality of life. The purpose of this study was to determine the life satisfaction of beta-thalassemic children and adolescents compared to healthy controls. METHODS This research, conducted in 2009, was a controlled, cross-sectional study in which beta-thalassemic patients, who were being followed-up by the Thalassemic Center in B...

Journal: :International Journal of Contemporary Pediatrics 2023

Background: Retarded growth in thalassemic patient is complex and multi-factorial, it includes chronic hypoxia secondary to anemia when pre-transfusion haemoglobin below 9 g/dl. Development of sexual characteristics children markedly delayed as compared their non-thalassemic siblings the expected development criteria due iron overload. The main objective present study monitor these patients lon...

Journal: :Diabetes care 2001
J P Chern K H Lin M Y Lu D T Lin K S Lin J D Chen C C Fu

OBJECTIVE To study the prevalence of and risk factors for abnormal glucose tolerance in transfusion-dependent beta-thalassemic patients. RESEARCH DESIGN AND METHODS A total of 89 transfusion-dependent beta-thalassemic patients were interviewed. Diabetes was previously diagnosed in 14 of them. In the remaining 75 patients, 68 participated in an oral glucose tolerance test. Potential risk facto...

Journal: :hepatitis monthly 0
bita behnava iran hepatitis network, tehran, ir iran; baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran heidar sharafi iran hepatitis network, tehran, ir iran; baqiyatallah research center for gastroenterology and liver diseases, baqiyatallah university of medical sciences, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran; armin pathobiology laboratory, tehran, ir iran maryam keshvari iran hepatitis network, tehran, ir iran; blood transfusion research center, high institute for research and education in transfusion medicine, tehran, ir iran ali pouryasin iran hepatitis network, tehran, ir iran; armin pathobiology laboratory, tehran, ir iran; department of biology, arsanjan branch, islamic azad university, arsanjan, ir iran leila mehrnoush iran hepatitis network, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran shima salimi iran hepatitis network, tehran, ir iran; middle east liver diseases (meld) center, tehran, ir iran

patients and methods this cross - sectional study was conducted on 143 thalassemic patients with chronic hepatitis c, who were treated with a combination of peg-ifn and rbv regimen. the rs12979860 and rs8099917 polymorphisms were assessed as the most common polymorphisms near the il28b gene by the polymerase chain reaction-restriction fragment length polymorphism (pcr-rflp) method. objectives w...

Journal: :Asian Pacific journal of allergy and immunology 2007
Sontana Siritantikorn Sujittra Kaewrawang Noppadol Siritanaratkul Apiradee Theamboonlers Yong Poovorawan Wannee Kantakamalakul Chantapong Wasi

Human parvovirus B19 infection was studied in 60 thalassemic patients in Thailand. Seroprevalence, persistence of parvovirus B19 and their genotypes were identified in blood samples. Prevalence of anti-parvovirus B19 IgG and DNA found in thalassemic patients were 38% and 13%, respectively. Anti-parvovirus B19 IgM could be detected in 4% of these positive anti-parvovirus B19 IgG patients. The se...

ژورنال: Medical Laboratory Journal 2007
Ahmadi, A, Bakhshandeh-Nosrat, S, Moradi,, A, Saeedi, M, Sanee- Moghaddam, E,

Abstract Background and objectives: HTLV-1 virus belongs to the retrovirus and infection with this virus mostly is seen among people having more than one time blood transfusion. Because of requiring repeated blood transfusions, thalassemic patients are considered to be high risk subjects in this regard. Thus, this study was carried out to indicate the frequency of HTLV-1 infection among the tha...

2010
Abolfazl Mahyar Parviz Ayazi Ali-Asghar Pahlevan Hoshyar Mojabi Mohammad-Reza Sehhat Amir Javadi

OBJECTIVE There are some reports in which a condition of zinc deficiency and its associated outcomes with a change in concentration of serum copper among the thalassemic patients has been highlighted. The aim of this prospective study was to determine the serum zinc and copper levels in children with beta-thalassemia major. METHODS In this cross sectional study all children under 12 years aff...

Journal: :Al-Azhar Journal of Pediatrics 2022

β-thalassemia is one of the most common hereditary diseases in Egypt. The leading causes renal dysfunction thalassemic patients include chronic anemia, iron overload from repeated blood transfusions, and kidney-induced damage use chelators.

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