- 関
- Mediterranean anemia、thalassaemia、thalassaemic、thalassemia
WordNet
- an inherited form of anemia caused by faulty synthesis of hemoglobin (同)thalassaemia, Mediterranean_anemia, Mediterranean anaemia
UpToDate Contents
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English Journal
- Tandem measurements of iron and creatinine by cross injection analysis with application to urine from thalassemic patients.
- Choengchan N1, Mantim T2, Inpota P3, Nacapricha D2, Wilairat P2, Jittangprasert P4, Waiyawat W2, Fucharoen S5, Sirankpracha P5, Morales NP6.
- Talanta.Talanta.2015 Feb;133:52-8. doi: 10.1016/j.talanta.2014.04.090. Epub 2014 Jul 7.
- This work presents development of a method for the dual determination of Fe(III) and creatinine using cross injection analysis (CIA). Two CIA platforms connected in series accommodated sample and reagents plugs aspirated via y-direction channels while water was pumped through the x-direction channel
- PMID 25435226
- Alpha thalassemia allelic frequency in Lebanon.
- Farra C1, Badra R, Fares F, Muwakkit S, Dbaibo G, Dabbous I, Ashkar H, Mounsef C, Abboud MR.
- Pediatric blood & cancer.Pediatr Blood Cancer.2015 Jan;62(1):120-2. doi: 10.1002/pbc.25242. Epub 2014 Oct 4.
- BACKGROUND: Hemoglobinopathies are the most common reported monogenic disorders worldwide. It is well established that Mediterranean and Arab countries are high risk areas for thalassemia in general, and for alpha thalassemia in particular. Reports of alpha thalassemia gene mutations from the Lebane
- PMID 25284125
- A genetic score for the prediction of beta-thalassemia severity.
- Danjou F1, Francavilla M2, Anni F2, Satta S3, Demartis FR2, Perseu L3, Manca M3, Sollaino MC3, Manunza L2, Mereu E2, Marceddu G2, Pissard S4, Joly P5, Thuret I6, Origa R2, Borg J7, Forni GL8, Piga A9, Lai ME3, Badens C10, Moi P2, Galanello R2.
- Haematologica.Haematologica.2014 Dec 5. pii: haematol.2014.113886. [Epub ahead of print]
- Clinical and hematological characteristics of beta-thalassemia are determined by several factors resulting in a wide spectrum of severity. Phenotype modulators are: HBB mutations, HBA defects and fetal hemoglobin production modulators (HBG2:g.-158C>T polymorphism, HBS1L-MYB intergenic region and
- PMID 25480500
Japanese Journal
- The profile of free amino acids in latent fingerprint of healthy and beta-thalassemic volunteers
- KHEDR Alaa
- Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 878(19), 1576-1582, 2010-06-01
- NAID 10028037402
- Hepatitis B virus reactivation during combined therapy with deferiprone and desferioxamine in a hepatitis B surface antigen thalassemic carrier
- RICCHI Paolo,CINQUE Patrizia,GALEOTA Alfonso Lanza,DI MATOLA Tiziana,AMMIRABILE Massimiliano,PROSSOMARITI Luciano
- International journal of hematology 89(2), 135-138, 2009-03-15
- NAID 10025159985
- Management of Spinal Cord Compression Caused by Extramedullary Hematopoiesis in Beta-thalassemia
- Moncef Berhouma,Hafedh Jemel
- Internal Medicine 47(12), 1125-1128, 2008
- … We present a case of EMH in a thalassemic adolescent boy presenting with a T12 level of compression, treated successfully with blood transfusion, surgical decompression and radiotherapy. …
- NAID 130000078862
Related Links
- Definition of THALASSEMIA: any of a group of inherited disorders of hemoglobin synthesis affecting the globin chain that are characterized usually by mild to severe hemolytic anemia, are caused by a series of allelic genes, and tend ...
- thal·as·se·mi·a (thăl′ə-sē′mē-ə) n. An inherited form of anemia occurring chiefly among people of Mediterranean descent, caused by faulty synthesis ... Chairman Ansar Burney Trust, Ansar Burney Advocate and thalassemic children ...
Related Pictures
★リンクテーブル★
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地中海貧血症、Mediterranean貧血症
- 関
- beta-thalassemia、Cooley's anemia、thalassaemia、thalassaemic、thalassemia、thalassemia major、thalassemia minor、thalassemic
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- 関
- Mediterranean anemia、thalassaemia、thalassemia、thalassemic