نتایج جستجو برای: deferasirox

تعداد نتایج: 613  

Journal: :Mediterranean Journal of Hematology and Infectious Diseases 2018

Journal: :Blood 2006
Ellis J Neufeld

For nearly 30 years, patients with transfusional iron overload have depended on nightly deferoxamine infusions for iron chelation. Despite dramatic gains in life expectancy in the deferoxamine era for patients with transfusion-dependent anemias, the leading cause of death for young adults with thalassemia major and related disorders has been cardiac disease from myocardial iron deposition. Stra...

2014
Tim G St Pierre Amal El-Beshlawy Mohsen Elalfy Abdullah Al Jefri Kusai Al Zir Shahina Daar Dany Habr Ulrike Kriemler-Krahn Ali Taher

PURPOSE Magnetic resonance imaging (MRI)-based techniques for assessing liver iron concentration (LIC) have been limited by single scanner calibration against biopsy. Here, the calibration of spin-density projection-assisted (SDPA) R2-MRI (FerriScan®) in iron-overloaded β-thalassemia patients treated with the iron chelator, deferasirox, for 12 months is validated. METHODS SDPA R2-MRI measurem...

2012
Russell E. Ware Ronald W. Helms

Stroke is a devastating complication of sickle cell anemia (SCA) with high recurrence if untreated. Chronic transfusions reduce recurrent strokes but have associated morbidities including iron overload. Stroke With Transfusions Changing to Hydroxyurea (SWiTCH) was a multicenter phase 3 randomized trial comparing standard treatment (transfusions/chelation) to alternative treatment (hydroxyurea/p...

Journal: :Molecular pharmacology 2015
Viktoryia Sidarovich Valentina Adami Pamela Gatto Valentina Greco Toma Tebaldi Gian Paolo Tonini Alessandro Quattrone

Iron is an essential cellular nutrient, being a critical cofactor of several proteins involved in cell growth and replication. Compared with normal cells, neoplastic cells have been shown to require a greater amount of iron, thus laying the basis for the promising anticancer activity of iron chelators. In this work, we evaluated the effects of molecules with iron chelation activity on neuroblas...

Journal: :The Southeast Asian journal of tropical medicine and public health 2011
Kitti Torcharus Tidarat Pankaew

Thalassemia is a chronic hereditary disease in which patients with severe disease present with anemia during their first year of life. In Thailand, stem cell transplantation is not an option for most patients. Supportive treatments, such as blood transfusions and iron chelation are used. Little data exists regarding the Health Related Quality of Life (HRQoL) of these patients. We conducted a st...

Journal: :Computational biology and chemistry 2016
Samie Salehi Amir Shokooh Saljooghi Mohammad Izadyar

Elemental iron is essential for cellular growth and homeostasis but it is potentially toxic to the cells and tissues. Excess iron can contribute in tumor initiation and tumor growth. Obviously, in iron overload issues using an iron chelator in order to reduce iron concentration seems to be vital. This study presents the density functional theory calculations of the electronic structure and equi...

Journal: :Blood 2010
Jong Wook Lee Sung-Soo Yoon Zhi Xiang Shen Arnold Ganser Hui-Chi Hsu Dany Habr Gabor Domokos Bernard Roubert John B Porter

The prospective 1-year Evaluation of Patients' Iron Chelation with Exjade (EPIC) study enrolled a large cohort of 116 patients with aplastic anemia; the present analyses evaluated the efficacy and safety of deferasirox in this patient population. After 1 year, median serum ferritin decreased significantly from 3254 ng/mL at baseline to 1854 ng/mL (P < .001). Decreases occurred in chelation-naiv...

2015
Muzamil Shabana Ejaz Shagufta Baloch Fehmina Arif

OBJECTIVE To determine the efficacy and adverse effects of oral chelation therapy (deferasirox) in multi-transfused β-thalassemia major patients visiting pediatric thalassemia clinic in Civil Hospital Karachi. METHODS This prospective study was conducted at pediatric thalassemia clinic of Civil Hospital Karachi. Hundred multi-transfused β-thalassemia patients registered in the clinic for oral...

2012
Ayumi Numata Masatsugu Tanaka Takayoshi Tachibana Kenji Matsumoto Atsuo Maruta Yoshiaki Ishigatsubo

A 41 ― year-old Japanese man with Philadelphia chromosome-positive acute lymphoblastic leukemia received allogeneic hematopoietic stem cell transplantation (allo-HSCT) from a human leukocyte antigen (HLA)-matched unrelated donor at molecular complete remission. Although bone marrow engraftment was successful, he required frequent red blood cell transfusions due to pure red cell aplasia followin...

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