地中海贫血患者的血清铁调素水平与中风 - Suppr

Serum hepcidin levels and stroke in thalassemia patients.

作者信息

Petrova Julia, Manolov Victor, Dimitrov Georgi, Tarnovska-Kadreva Rumiana, Yaneva-Sirakova Theodora, Velizarova Milena, Vasilev Vasil, Atanasova Bisera, Tzatchev Kamen, Marinov Borislav, Emilova Radoslava, Genchev Gencho

机构信息

Department of Neurology, Medical University, Sofia, Bulgaria.

Department of Medical Genetics, Medical University, Sofia, Bulgaria

出版信息

Int J Stroke. 2016 Jun;11(4):NP50-1. doi: 10.1177/1747493015623557. Epub 2016 Jan 5.

DOI:10.1177/1747493015623557

PMID:26763924

Abstract

摘要

相似文献

Serum hepcidin levels and stroke in thalassemia patients.

Int J Stroke. 2016 Jun;11(4):NP50-1. doi: 10.1177/1747493015623557. Epub 2016 Jan 5.

Serum Hepcidin as a Diagnostic Marker of Severe Iron Overload in Beta-thalassemia Major.

Indian J Pediatr. 2017 Oct;84(10):745-750. doi: 10.1007/s12098-017-2375-4. Epub 2017 Jun 10.

Serum Hepcidin Levels in Children with Beta Thalassemia Major.

Indian Pediatr. 2018 Oct 15;55(10):911-912. Epub 2018 Jun 13.

Evaluation of Erythroferrone, Hepcidin, and Iron Overload Status in Iraqi Transfusion-Dependent β-Thalassemia Major Patients.

Hemoglobin. 2020 Jul;44(4):272-277. doi: 10.1080/03630269.2020.1794888. Epub 2020 Jul 27.

Correlation of hepcidin level with insulin resistance and endocrine glands function in major thalassemia.

Adv Clin Exp Med. 2015 Jan-Feb;24(1):69-78. doi: 10.17219/acem/38158.

Peripheral expression of hepcidin gene in Egyptian β-thalassemia major.

Gene. 2015 Jun 15;564(2):206-9. doi: 10.1016/j.gene.2015.03.048. Epub 2015 Mar 25.

Genetic modifiers of secondary iron overload in beta thalassemia major.

Blood Cells Mol Dis. 2015 Mar;54(3):242-3. doi: 10.1016/j.bcmd.2014.12.006. Epub 2015 Jan 8.

Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia.

Haematologica. 2015 May;100(5):e169-71. doi: 10.3324/haematol.2014.115733. Epub 2015 Jan 16.

Hepcidin levels and iron status in beta-thalassemia major patients with hepatitis C virus infection.

Egypt J Immunol. 2010;17(2):33-44.

Erythroferrone, the new iron regulator: evaluation of its levels in Egyptian patients with beta thalassemia.

Ann Hematol. 2020 Jan;99(1):31-39. doi: 10.1007/s00277-019-03882-w. Epub 2019 Dec 13.

引用本文的文献

Glutamate, Glutamine, GABA and Oxidative Products in the Pons Following Cortical Injury and Their Role in Motor Functional Recovery.

Neurochem Res. 2021 Dec;46(12):3179-3189. doi: 10.1007/s11064-021-03417-8. Epub 2021 Aug 13.

Hepcidin: A Promising Therapeutic Target for Iron Disorders: A Systematic Review.

Medicine (Baltimore). 2016 Apr;95(14):e3150. doi: 10.1097/MD.0000000000003150.

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Serum hepcidin levels and stroke in thalassemia patients.

作者信息

机构信息

Department of Neurology, Medical University, Sofia, Bulgaria.

Department of Medical Genetics, Medical University, Sofia, Bulgaria

出版信息

Int J Stroke. 2016 Jun;11(4):NP50-1. doi: 10.1177/1747493015623557. Epub 2016 Jan 5.

DOI:10.1177/1747493015623557

PMID:26763924

Abstract

摘要

相似文献

Serum hepcidin levels and stroke in thalassemia patients.

Int J Stroke. 2016 Jun;11(4):NP50-1. doi: 10.1177/1747493015623557. Epub 2016 Jan 5.

Serum Hepcidin as a Diagnostic Marker of Severe Iron Overload in Beta-thalassemia Major.

Indian J Pediatr. 2017 Oct;84(10):745-750. doi: 10.1007/s12098-017-2375-4. Epub 2017 Jun 10.

Serum Hepcidin Levels in Children with Beta Thalassemia Major.

Indian Pediatr. 2018 Oct 15;55(10):911-912. Epub 2018 Jun 13.

Evaluation of Erythroferrone, Hepcidin, and Iron Overload Status in Iraqi Transfusion-Dependent β-Thalassemia Major Patients.

Hemoglobin. 2020 Jul;44(4):272-277. doi: 10.1080/03630269.2020.1794888. Epub 2020 Jul 27.

Correlation of hepcidin level with insulin resistance and endocrine glands function in major thalassemia.

Adv Clin Exp Med. 2015 Jan-Feb;24(1):69-78. doi: 10.17219/acem/38158.

Peripheral expression of hepcidin gene in Egyptian β-thalassemia major.

Gene. 2015 Jun 15;564(2):206-9. doi: 10.1016/j.gene.2015.03.048. Epub 2015 Mar 25.

Genetic modifiers of secondary iron overload in beta thalassemia major.

Blood Cells Mol Dis. 2015 Mar;54(3):242-3. doi: 10.1016/j.bcmd.2014.12.006. Epub 2015 Jan 8.

Differences in the erythropoiesis-hepcidin-iron store axis between hemoglobin H disease and β-thalassemia intermedia.

Haematologica. 2015 May;100(5):e169-71. doi: 10.3324/haematol.2014.115733. Epub 2015 Jan 16.

Hepcidin levels and iron status in beta-thalassemia major patients with hepatitis C virus infection.

Egypt J Immunol. 2010;17(2):33-44.

Erythroferrone, the new iron regulator: evaluation of its levels in Egyptian patients with beta thalassemia.

Ann Hematol. 2020 Jan;99(1):31-39. doi: 10.1007/s00277-019-03882-w. Epub 2019 Dec 13.

引用本文的文献

Glutamate, Glutamine, GABA and Oxidative Products in the Pons Following Cortical Injury and Their Role in Motor Functional Recovery.

Neurochem Res. 2021 Dec;46(12):3179-3189. doi: 10.1007/s11064-021-03417-8. Epub 2021 Aug 13.

Hepcidin: A Promising Therapeutic Target for Iron Disorders: A Systematic Review.

Medicine (Baltimore). 2016 Apr;95(14):e3150. doi: 10.1097/MD.0000000000003150.

Serum hepcidin levels and stroke in thalassemia patients.

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Serum hepcidin levels and stroke in thalassemia patients.

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