نتایج جستجو برای: intermedia β

تعداد نتایج: 180489  

2002
Corina Hartman Hannah Tamary Carina Levine Raanan Shamir

Low plasma levels of total cholesterol (TC) with or without hypertriglyceridemia have been frequently described in a variety of hematologic disorders in which anemia is a prominent feature.2,3 It is well established that β-thalassemia is associated with changes in plasma lipids and lipoproteins. In β-thalassemia major, low cholesterol levels caused by a significant reduction of both low-density...

Journal: :iranian journal of pediatric hematology and oncology 0
n valizadeh assistant professor of hematology/medical oncology, urmia university of medical sciences, urmia, iran f farrokhi medical student, urmia university of medical sciences, urmia, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ارومیه (urmia university of medical sciences) v alinejad msc. of biostatistics, patient safety research center, urmia university of medical sciences, urmia, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ارومیه (urmia university of medical sciences) sm said mardani assistant professor of rheumatology, urmia university of medical sciences, urmia, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ارومیه (urmia university of medical sciences) n valizadeh assistant professor of endocrinology and metabolism, urmia university of medical sciences, urmia, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی ارومیه (urmia university of medical sciences) s hejazi assistant professor of pediatric hematology/medical oncology, department of pediatric hematology, motahari hospital, urmسازمان اصلی تایید شده: دانشگاه علوم پزشکی ارومیه (urmia university of medical sciences)

background patients with thalassemia major and intermedia are susceptible to osteopenia and osteoporosis. the mechanism of osteoporosis in these patients is multifactorial. transfusion related iron overload in endocrine organs leads to impaired growth hormone secretion, diabetes mellitus, hypothyroidism, hypoparathyroidism, lack of sex steroids and vitamin d deficiency that contribute to impair...

F Farrokhi, M Noroozi, N Valizadeh, S Hejazi, SM Said Mardani, V Alinejad,

Background Patients with thalassemia major and intermedia are susceptible to osteopenia and osteoporosis. The mechanism of osteoporosis in these patients is multifactorial. Transfusion related iron overload in endocrine organs leads to impaired growth hormone secretion, diabetes mellitus, hypothyroidism, hypoparathyroidism, lack of sex steroids and vitamin D deficiency that contribute t...

2017
João Guardado Correia Nídia Moreira Carlos Eduardo Costa Almeida Luís Simões Reis

Introduction Thalassemia is a common disease which treatment is often based on splenectomy. The risks associated with total splenectomy stimulated partial splenectomy as a potentially alternative therapy. Case presentation A 45 year-old female patient with long term follow-up for β thalassemia intermedia started to develop signs of hypersplenism and iron overload. A partial splenectomy was pe...

2014
N Valizadeh F Farrokhi V Alinejad SM Said Mardani N Valizadeh S Hejazi M Noroozi

BACKGROUND Patients with thalassemia major and intermedia are susceptible to osteopenia and osteoporosis. The mechanism of osteoporosis in these patients is multifactorial. Transfusion related iron overload in endocrine organs leads to impaired growth hormone secretion, diabetes mellitus, hypothyroidism, hypoparathyroidism, lack of sex steroids and vitamin D deficiency that contribute to impair...

Aliakbar Modarres, Khadijeh Arjmandi Rafsanjani, Leila Zahedi-Shoolami, Maryam Razzaghy-Azar, Nima Taheri, Parvaneh Vossough,

Background: Expansion of bone marrow cavity and decreased cortical and trabecular bone tissues and osteoporosis are resulted from beta-thalassemia. The aim of this study was to assess bone mineral density (BMD) in patients with β thalassemia major and intermedia, and to determine their biochemical and hormonal profiles that may affect BMD. Materials and Methods: In a cross sectional study from ...

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