WordNet
- first in order of importance; "the alpha male in the group of chimpanzees"; "the alpha star in a constellation is the brightest or main star"
- the 1st letter of the Greek alphabet
- the beginning of a series or sequence; "the Alpha and Omega, the first and the last, the beginning and the end"--Revelations
- early testing stage of a software or hardware product; "alpha version"
- any high mountain
PrepTutorEJDIC
- アルファ(ギリシア語アルファベットの第1字A,α;英語のA,aに相当) / アルファ星(星座の主星)
- 高山,高峰
UpToDate Contents
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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. αサラセミアの病態生理 pathophysiology of alpha thalassemia
- 3. サラセミア症候群の分子病理 molecular pathology of the thalassemic syndromes
- 4. 異型鎌状赤血球症候群 variant sickle cell syndromes
- 5. 鎌状細胞貧血における臨床的ばらつき clinical variability in sickle cell anemia
English Journal
- Deferiprone versus deferoxamine in thalassemia intermedia: Results from a 5-year long-term Italian multicenter randomized clinical trial.
- Calvaruso G1, Vitrano A1, Di Maggio R1, Lai E2, Colletta G3, Quota A4, Gerardi C5, Rigoli LC6, Sacco M1, Pitrolo L1, Maggio A1.
- American journal of hematology.Am J Hematol.2015 Jul;90(7):634-8. doi: 10.1002/ajh.24024. Epub 2015 May 3.
- In patients with thalassemia intermedia (TI), such as beta-TI, alpha-thalassemia (mainly HbH disease and mild/moderate forms of HbE/beta-thalassemia), iron overload is an important challenge in terms of diagnosis, monitoring, and treatment. Moreover, to date, the only possible chelators available ar
- PMID 25809173
- Hb Cervantes, Hb Marañón, Hb La Mancha and Hb Goya: Description of 4 new haemoglobinopathies.
- de la Fuente-Gonzalo F1, Nieto JM2, Ricard P3, Anguita J4, Martínez R5, Cervera A6, Villegas A2, González FA2, Ropero P2.
- Clinical biochemistry.Clin Biochem.2015 Jul;48(10-11):662-7. doi: 10.1016/j.clinbiochem.2015.04.020. Epub 2015 May 2.
- OBJECTIVES: α-thalassemias are caused by a deficiency in or absence of synthesis of the α-chain of haemoglobin (Hb). In contrast, structural haemoglobinopathies are due to mutations that change the amino acid sequence of the protein chain. We report 4 newly identified α-chain Hb variants. Two var
- PMID 25943047
- Incidence of hemoglobinopathies and thalassemias in Northern Alberta. Establishment of reference intervals for HbF and HbA2.
- Rodriguez-Capote K1, Higgins TN2.
- Clinical biochemistry.Clin Biochem.2015 Jul;48(10-11):698-702. doi: 10.1016/j.clinbiochem.2015.04.001. Epub 2015 Apr 11.
- OBJECTIVES: The aims of this study were to identify the incidence of hemoglobinopathies and thalassemias in Northern Alberta and calculate the reference intervals (RI) for hemoglobin (Hb) HbF and HbA2.METHODS: A retrospective ad-hoc analysis of the structural Hb variants and thalassemias identified
- PMID 25869492
Japanese Journal
- Localization of the Chromatin Remodelling Protein, ATRX in the Adult Testis
- Journal of Reproduction and Development 57(3), 317-321, 2011
- NAID 130000130590
- Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism
- Journal of human genetics 53(6), 524-528, 2008-06-01
- NAID 10021249288
- Complementation of alpha-thalassaemia in alpha-globin knockout mice with a 191 kb transgene containing the human alpha-globin locus
- Transgenic Res. 13, 235-243, 2004
- NAID 30012892775
Related Links
- Alpha thalassemia occurs when some or all of the 4 genes that make hemoglobin (the alpha-globin genes) are missing or damaged. There are 4 types of alpha thalassemia: Alpha thalassemia silent carrier. One gene is missing or damaged, and the other 3 are normal.
- Couples who are members of populations at risk for α-thalassemia trait with a two-gene deletion in cis (--/αα) can be identified prior to pregnancy as being at risk of conceiving a fetus with Hb Bart syndrome.
- Alpha-thalassemia is a blood disorder that reduces the body's production of hemoglobin. Affected people have anemia , which can cause pale skin, weakness, fatigue, and more serious complications. Two types of alpha-thalassemia can cause health problems: the more severe type is known as Hb Bart syndrome ; the milder form is called HbH disease.
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★リンクテーブル★
| リンク元 | 「αサラセミア」 |
| 関連記事 | 「alpha」 |
「αサラセミア」
- 英
- alpha thalassemia, alpha-thalassemia, α thalassemia, α-thalassemia. alpha-thalassaemia
- 関
- アルファサラセミア、α地中海貧血症、ヘモグロビンH症、α-サラセミア、サラセミア、hemoglobin H disease HbH病
- ヘモグロビンα鎖グロビンの合成障害による先天性貧血
「alpha」
- 関
- alfa