Výsledky vyhledávání - "Marzieh Bardestani"

Relationship Between Serum Hepcidin and Ferritin Levels in Patients With Thalassemia Major and Intermedia in Southern Iran

Autor: Javad Dehbozorgian, Sanaz Safaei, Maryam Abdollahi, Narges Rezaei, Sezaneh Haghpanah, Marzieh Bardestani, Fatemeh Hassani, Naser Honar, Mehran Karimi, Masoomeh Esmaeilzadeh

Publikováno v: Iranian Red Crescent Medical Journal

Background: Hepcidin is a key regulator of iron absorption in humans. It is mainly affected by hypoxia and iron stores. Objectives: The current study aimed to determine the correlation between serum hepcidin and ferritin levels in patients with Thala

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c4c637631b79dff8ad2181d477f565a
https://doi.org/10.5812/ircmj.17(5)2015.28343

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Serum Ferritin Levels Correlation With Heart and Liver MRI and LIC in Patients With Transfusion-Dependent Thalassemia

Autor: Sezaneh Haghpanah, Gholamhossein Ajami, Sara Matin, Zahra Majd, Marzieh Bardestani, Mehran Karimi, Hamid Namazi

Publikováno v: Iranian Red Crescent Medical Journal

Background: Iron-loaded cardiac complication is the essential cause of mortality in patients with thalassemia. Early detection and treatment of cardiac over-load can reduce mortality. Objectives: The current study aimed to evaluate the relationship b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6ac974cdb5d4574dd3810acf445eb06
https://doi.org/10.5812/ircmj.17(4)2015.24959

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Comparative Study of Radiographic and Laboratory Findings Between Beta Thalassemia Major and Beta Thalassemia Intermedia Patients With and Without Treatment by Hydroxyurea

Autor: Amin Abolhasani Foroughi, Masoume Nazeri, Mehran Karimi, Sezaneh Haghpanah, Roghieh Ghaffari, Marzieh Bardestani, Hosein Ghaffari

Publikováno v: Iranian Red Crescent Medical Journal

Background: In patients with thalassemia, chronic anemia causes bone marrow expansion and consequently skeletal manifestation in spine, skull, face and rib bones. Objectives: We aimed to compare chest radiographic findings and facial bone deformity i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::872b55f61199b38933d669fa565ced9e
https://doi.org/10.5812/ircmj.23607

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Frequency of Cholelithiasis in Patients With Beta-Thalassemia Intermedia With and Without Hydroxyurea

Autor: Sezaneh Haghpanah, Azin Hamidi, Mehran Karimi, Marzieh Bardestani, Maryam Khavari, Mohammad Hadi Bagheri, Razieh Hantooshzadeh

Publikováno v: Iranian Red Crescent Medical Journal

Background: Recent studies regarding the effect of hydroxyurea (HU) in thalassemia have revealed favorable effects on the reduction of ineffective erythropoiesis. Objectives: The aim of the current study was to evaluate whether or not HU can have an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9256fa74364510b2ea18057bf3fdb867
http://europepmc.org/articles/PMC4166105

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Hydroxyurea Treatment in Transfusion-Dependent β-Thalassemia Patients

Autor: Roza Kamfiroozi, Samir Silavizadeh, Marzieh Bardestani, Mohammadreza Bordbar, Sezaneh Haghpanah, Mehran Karimi

Publikováno v: Iranian Red Crescent Medical Journal

Background: β-Thalassemia is an inherited hemoglobin disorder caused by defective synthesis of s-globin chains. Hemoglobin (Hb) F induction is a possible therapeutic approach which can partially compensate for α and non-α globin chains imbalance.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf32e6da0075b6b55fc80aa2f283dd41
http://europepmc.org/articles/PMC4102988

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