نتایج جستجو برای: iron overload

تعداد نتایج: 159833  

Journal: :Blood 2009
Steven Bair Emily Spaulding Jaakko Parkkinen Howard M Shulman Vladimir Lesnikov Mary Beauchamp François Canonne-Hergaux Kris V Kowdley H Joachim Deeg

Iron overload is common in patients undergoing allogeneic hematopoietic cell transplantation (HCT), but the mechanisms leading to overload are unknown. Here, we determined iron levels and the expression of iron regulatory proteins in the liver and gut of nonobese diabetic-severe combined immunodeficient (NOD/SCID) mice that underwent transplantation with syngeneic (histocompatible) or allogenei...

2016
Guy Rostoker Nosratola D. Vaziri Steven Fishbane

Iron overload used to be considered rare in hemodialysis patients but its clinical frequency is now increasingly realized. The liver is the main site of iron storage and the liver iron concentration (LIC) is closely correlated with total iron stores in patients with secondary hemosideroses and genetic hemochromatosis. Magnetic resonance imaging is now the gold standard method for LIC estimation...

Journal: :The Journal of clinical investigation 1991
B M Myers F G Prendergast R Holman S M Kuntz N F LaRusso

While hemochromatosis is characterized by sequestration of iron-protein complexes in hepatocyte lysosomes, little is known about the effects of excess iron on these organelles. Therefore, we studied the effects of experimental iron overload on hepatocyte lysosomal structure, physicochemical properties, and function in rats fed carbonyl iron. A sixfold increase (P less than 0.0001) in hepatic ir...

Journal: :Blood 2012
Emilio Ramos Piotr Ruchala Julia B Goodnough Léon Kautz Gloria C Preza Elizabeta Nemeth Tomas Ganz

The deficiency of hepcidin, the hormone that controls iron absorption and its tissue distribution, is the cause of iron overload in nearly all forms of hereditary hemochromatosis and in untransfused iron-loading anemias. In a recent study, we reported the development of minihepcidins, small drug-like hepcidin agonists. Here we explore the feasibility of using minihepcidins for the prevention an...

Journal: :Nihon Naika Gakkai Zasshi 2011

2017
Nripendranath Mandal Bibhabasu Hazra Rhitajit Sarkar

Excess iron deposition in the liver catalyses the production of Reactive Oxygen Species (ROS) which in turn initiate oxidative damage of protein and nucleic acids leading to several human diseases. The fruits of Terminalia Belerica Roxb. (TB) has been most commonly used not only in stimulating gastrointestinal health, but also in treatment of various hepatic disorders. The present study was aim...

2011
Shinya Toyokuni

Persistent oxidative stress has been associated with carcinogenesis. Iron overload is considered one such condition that causes oxidative stress. Epidemiological studies support a close link between iron overload and carcinogenesis. Reportedly, regular semiannual phlebotomies reduced cancer risk in an otherwise normal population. More specifically, genetic hemochromatosis, chronic viral hepatit...

2013
Reijâne Alves de Assis Carolina Kassab Fernanda Salles Seguro Fernando Ferreira Costa Paulo Augusto Achucarro Silveira John Wood Nelson Hamerschlak

To report a case of iron overload secondary to xerocytosis, a rare disease in a teenager, diagnosed, by T2* magnetic resonance imaging. We report the case of a symptomatic patient with xerocytosis, a ferritin level of 350ng/mL and a significant cardiac iron overload. She was diagnosed by T2* magnetic resonance imaging and received chelation therapy Ektacytometric analysis confirmed the diagnosi...

2017
Mürüvvet Seda Aydın Süreyya Bozkurt Gürsel Güneş Ümit Yavuz Malkan Tuncay Aslan Sezgin Etgül Yahya Büyükaşık İbrahim Celalettin Haznedaroğlu Nilgün Sayınalp Hakan Göker Haluk Demiroğlu Osman İlhami Özcebe Salih Aksu

Thank you very much for your valuable comments and sharing your experience. We agree for your contribution. In thalassemia patients, several transplantation centers categorised risk factors prior to allogenic hematopoietic stem cell transplantation. Pesaro classification assigned patients to three arms according to the absence or presence of one, two or three risk factors: hepatomegaly > 2 cm, ...

2014
Maja Vujić

Iron-overload disorders owing to genetic misregulation of iron acquisition are referred to as hereditary hemochromatosis (HH). The most prevalent genetic iron overload disorder in Caucasians is caused by mutations in the HFE gene, an atypical MHC class I molecule. Recent studies classified HFE/Hfe-HH as a liver disease with the primarily failure in the production of the liver iron hormone hepci...

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