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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/01/20 13:52:12」(JST)

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  • Rapid detection of non-deletional mutations causing α-thalassemia by multicolor melting curve analysis.
  • Huang Q, Wang X, Tang N, Zhu C, Yan T, Chen P, Li Q.
  • Clinical chemistry and laboratory medicine.Clin Chem Lab Med.2016 Mar 1;54(3):397-402. doi: 10.1515/cclm-2015-0173.
  • BACKGROUND: α-Thalassemia, caused by mutations in the α-globin genes, is one of the most common monogenic inherited disorders in the world. However, non-deletional α-thalassemia mutations remain undetected in routine clinical testing due to the lack of a suitable method. In this study, a closed-
  • PMID 26351923
  • The Effect of Hydroxyurea Therapy in Bahraini Sickle Cell Disease Patients.
  • Shome DK1, Al Ajmi A2, Radhi AA3, Mansoor EJ3, Majed KS3.
  • Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.Indian J Hematol Blood Transfus.2016 Mar;32(1):104-9. doi: 10.1007/s12288-015-0529-y. Epub 2015 Mar 18.
  • Hydroxyurea (HU) is used as a disease-modifying agent in sickle cell disease (SCD). Its beneficial effects have been ascribed to inhibition of the sickling process through increase of fetal hemoglobin (HbF) levels and influence on multiple factors affecting adhesion of erythrocytes to vascular endot
  • PMID 26855516
  • Evaluation of α-Globin Gene Mutations Among Different Ethnic Groups in Khuzestan Province, Southwest Iran.
  • Khosravi A1, Jalali-Far M2, Saki N2, Hosseini H2, Galehdari H2, Kiani-Ghalesardi O2, Paridar M3, Azarkeivan A4, Magaji-Hamid K5,6.
  • Hemoglobin.Hemoglobin.2016 Feb 15:1-5. [Epub ahead of print]
  • α-Thalassemia (α-thal) is one of the most common inherited hemoglobin (Hb) disorders in the world. In addition to large deletions, over 50 different α-thal point mutations were detected around the world, thus, patients showed different phenotypes with regard to genotype. This study evaluated the
  • PMID 26878087


  • αサラセミアによる胎児水腫を呈したベトナム人妊婦の一例
  • 嶋田 亜公子,矢木 さやか,京谷 琢治,高木 剛,丸山 憲一
  • 日本周産期・新生児医学会雑誌 = Journal of Japan Society of Perinatal and Neonatal Medicine 48(3), 734-738, 2012-08-30
  • NAID 10031048871
  • Aortic Valve Replacement in a Patient with Alpha-Thalassemia
  • OMOTO Tadashi,TEDORIYA Takeo,KONDO Yasuyuki,IZUKA Hirofumi,OI Masaya,NAGANO Naoko,MIYAUCHI Tadamasa,ISHIKAWA Noboru,KASEGAWA Hitoshi
  • Annals of thoracic and cardiovascular surgery 16(5), 365-366, 2010-10-01
  • NAID 10029685909
  • 心拡大と胎児水腫を呈した胎児αサラセミアの一例
  • 久須美 真紀,加藤 有美,高橋 宏典,三浦 裕美子,林 聡,大石 芳久,高橋 重裕,中村 知夫,伊藤 裕司,山口 晃史,松岡 健太郎,服部 幸夫,山城 安啓,左合 治彦,北川 道弘
  • 日本周産期・新生児医学会雑誌 = Journal of Japan Society of Perinatal and Neonatal Medicine 44(4), 1241-1245, 2008-12-25
  • NAID 10025167361


Alpha-thalassemia (α-thalassemia) is a form of thalassemia involving the genes HBA1 and HBA2. Alpha-thalassemia is due to impaired production of 1,2,3, or 4 alpha globin chains, leading to a relative excess of beta globin chains.
Alpha thalassemia is a blood disorder that reduces the production of hemoglobin. Hemoglobin is the protein in red blood cells that carries oxygen to cells throughout the body. In people with the characteristic features of alpha thalassemia, ...






alpha thalassemia, alpha-thalassemia, α thalassemia, α-thalassemia. alpha-thalassaemia
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











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「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"」

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「the 1st letter of the Greek alphabet」

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「the beginning of a series or sequence; "the Alpha and Omega, the first and the last, the beginning and the end"--Revelations」

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「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)」

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「early testing stage of a software or hardware product; "alpha version"」


  [★] サラセミア

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「an inherited form of anemia caused by faulty synthesis of hemoglobin」
thalassaemia, Mediterranean anemia, Mediterranean anaemia



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「any high mountain」

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