WordNet

an inherited form of anemia caused by faulty synthesis of hemoglobin (同)thalassaemia, Mediterranean_anemia, Mediterranean anaemia

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1. サラセミアの臨床症状および診断 clinical manifestations and diagnosis of the thalassemias
2. βサラセミアの治療 treatment of beta thalassemia
3. αサラセミアの病態生理 pathophysiology of alpha thalassemia
4. βサラセミアの病態生理 pathophysiology of beta thalassemia
5. サラセミアおよびその他の鉄過剰状態に対するキレート療法 chelation therapy for thalassemia and other iron overload states

English Journal

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

Aboul-Enein A1, El-Beshlawy A2, Hamdy M2, Shaheen I1, El-Saadany Z1, Samir A3, El-Samie HA1.
Gene.Gene.2015 Jun 15;564(2):206-9. doi: 10.1016/j.gene.2015.03.048. Epub 2015 Mar 25.
Iron overload is the major cause of morbidity and mortality in transfusion dependent β-thalassemia major patients. There is a sophisticated balance of body iron metabolism of storage and transport which is regulated by several factors including the peptide hepcidin. Hepcidin is the main iron regula
PMID 25816754

Endothelial nitric oxide synthase gene intron 4 variable number tandem repeat polymorphism in β-thalassemia major: relation to cardiovascular complications.

Tantawy AA1, Adly AA, Ismail EA, Aly SH.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.Blood Coagul Fibrinolysis.2015 Jun;26(4):419-25. doi: 10.1097/MBC.0000000000000277.
Endothelial nitric oxide synthase (eNOS), an enzyme that generates nitric oxide, is a major determinant of endothelial function. Several eNOS gene polymorphisms have been reported as 'susceptibility genes' in various human diseases states, including cardiovascular, pulmonary and renal diseases. We s
PMID 25699607

Implementation of newborn screening for hemoglobin h disease in mainland china.

Xie XM1, Zhou JY1, Li J1, Li R1, Liao C1, Li DZ1.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.Indian J Hematol Blood Transfus.2015 Jun;31(2):242-6. doi: 10.1007/s12288-014-0432-y. Epub 2014 Jul 20.
Hemoglobin H disease is the most severe non-fatal form of α-thalassemia syndrome characterized by pronounced microcytic hypochromic hemolytic anemia. It is predominantly seen in Southeast Asia, the Middle East and the Mediterranean. Studies suggest that hemoglobin H disease is not as benign a disor
PMID 25825565

Japanese Journal

High prevalence of hepatitis C in patients with thalassemia and patients with liver diseases in Myanmar (Burma).

Okada Shigeru,Taketa Kazuhisa,Ishikawa Takatoshi,Koji Takehiko,Swe Than,Win Ne,Win Khin Maung,Mra Rai,Myint Thein Thein
Acta Medica Okayama 54(3), 2000-06-00
… <p>We conducted Myanmar-Japan cooperation studies on hepatitis B and hepatitis C virus markers in patients with thalassemias and those with liver diseases. …
NAID 120002311466

The β-thalassemias

OLIVIERI NF
N Engl J Med 341, 99-109, 1999
NAID 30022553883

Molecular Analysis of Common Types ofﾎｱ-Thalassemia Associated with(ﾎｲ-Thalassemia in Northern Thailand

Kudeken Mika,Asato Tsuyoshi,Tsuda Satoshi,Nakashima Yasutsugu,Takei Hiroshi,Buasaengchan Suwanna,Makonkawkeyoon Luksana
Acta medica Nagasakiensia 43(1-2), 33-37, 1998-06-00
… whereas the (ﾎｲ-thalassemias withﾎｱ-globin gene defects in both alleles showed less severe anemia. …
NAID 110000013819

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