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English Journal
- A Novel α2-Globin Gene Mutation: Hb Debao [α31(B12)Arg→Trp; HBA2: c.94A>T].
 
- Lin L1, Chen B1, Yi S1, Chen Q1, Wei H1, Li G2, Zheng C1, Qiu XX1, He S1.
 
- Hemoglobin.Hemoglobin.2017 Apr 2:1-3. doi: 10.1080/03630269.2017.1289102. [Epub ahead of print]
 
- PMID 28367658
 
- [Neonatal expression of beta-thalassemia trait associated with hereditary spherocytosis in two monozygotic twins].
 
- Ben Hamouda H1, Mahjoub B2, Soua H2, Laradi S3, Miled A3, Sfar MT2.
 
- Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.Arch Pediatr.2017 Feb;24(2):126-130. doi: 10.1016/j.arcped.2016.10.024. Epub  2016 Dec 12.
 
- PMID 27979672
 
- A Mouse Model for Human Unstable Hemoglobin Santa Ana.
 
- Miyashiro SI1, Massironi SM2, Mori CM3, Cruz CC2, Hagiwara MK1, Maiorka PC2.
 
- Comparative medicine.Comp Med.2016 Dec 1;66(6):437-444.
 
- PMID 28304246
 
Japanese Journal
- 栄養介入による男子大学生長距離ランナーの貧血指標の改善
 
- An Automated Hb A_2 Analyzer, HLC-723G7, for Diagnosis of β-Thalassemia
 
- 生後早期に遺伝子解析により診断されたヘモグロビンE症の1男児例
 
Related Pictures







★リンクテーブル★
  [★]
- 英
 
- hypochromia、hypochromic
 
- 関
 
- 血色素減少、低色素血
 
  [★]
- 英
 
- hypochromia
 
- 関
 
- 血色素減少、低色素
 
  [★]
- 英
 
- hypochromia
 
- 関
 
- 低色素、低色素血
 
  [★]
- 関
 
- hypochromia