These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
184 related items for PubMed ID: 24229410
1. Newborn screening for Hb H disease by determination of Hb Bart's using the Sebia capillary electrophoresis system in southern China. Liao C, Zhou JY, Xie XM, Tang HS, Li R, Li DZ. Hemoglobin; 2014; 38(1):73-5. PubMed ID: 24229410 [Abstract] [Full Text] [Related]
3. Neonatal screening for α-thalassemia by cord hemoglobin Barts: how effective is it? Wu MY, Xie XM, Li J, Li DZ. Int J Lab Hematol; 2015 Oct; 37(5):649-53. PubMed ID: 25955662 [Abstract] [Full Text] [Related]
6. Prevention of Hb Bart's (γ4) Disease Associated with the - -(THAI) α(0)-Thalassemia Deletion in Mainland China. Li DZ, Li Y, Li J, Li SC, Li R. Hemoglobin; 2015 Oct; 39(6):412-4. PubMed ID: 26212676 [Abstract] [Full Text] [Related]
8. Neonatal screening for alpha-thalassemia in southern Taiwan. Lin TM, Eng HL, Kuo PL, Wu HL. J Formos Med Assoc; 1992 Dec; 91(12):1213-5. PubMed ID: 1363647 [Abstract] [Full Text] [Related]
9. Cord blood screening for alpha-thalassemia and hemoglobin variants by isoelectric focusing in northern Thai neonates: correlation with genotypes and hematologic parameters. Charoenkwan P, Taweephol R, Sirichotiyakul S, Tantiprabha W, Sae-Tung R, Suanta S, Sakdasirisathaporn P, Sanguansermsri T. Blood Cells Mol Dis; 2010 Jun 15; 45(1):53-7. PubMed ID: 20299254 [Abstract] [Full Text] [Related]
11. Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots. Jindatanmanusan P, Riolueang S, Glomglao W, Sukontharangsri Y, Chamnanvanakij S, Torcharus K, Viprakasit V. Ann Clin Biochem; 2014 Mar 15; 51(Pt 2):237-47. PubMed ID: 23901141 [Abstract] [Full Text] [Related]
12. Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR. Wang W, Yap CH, Loh SF, Tan AS, Lim MN, Prasath EB, Chan ML, Tan WC, Jiang B, Yeo GH, Mathew J, Ho A, Ho SS, Wong PC, Choolani MA, Chong SS. Reprod Biomed Online; 2010 Nov 15; 21(5):642-8. PubMed ID: 20864413 [Abstract] [Full Text] [Related]
14. Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): two novel alpha2 gene mutations associated with mild alpha-thalassemia found in the same family after newborn screening. Giordano PC, Cnossen MH, Joosten AM, Jansen CA, Hakvoort TE, Bakker-Verweij M, Arkesteijn SG, van Delft P, Waye JS, Bouva MJ, Harteveld CL. Hemoglobin; 2010 Nov 15; 34(4):354-65. PubMed ID: 20642333 [Abstract] [Full Text] [Related]
18. Hemoglobin Lepore EF Bart's disease: a molecular, hematological, and diagnostic aspects. Chaibunruang A, Fucharoen G, Jetsrisuparb A, Fucharoen S. Ann Hematol; 2011 Nov 15; 90(11):1337-40. PubMed ID: 21302111 [Abstract] [Full Text] [Related]
19. Four cases of Hb Q-H disease found in Southern China. Li D, Liao C, Xie X, Zhong H, Li J. Hemoglobin; 2007 Nov 15; 31(1):109-11. PubMed ID: 17365013 [Abstract] [Full Text] [Related]
20. Early onset of fetal hydrops associated with the α-thalassemia - -(THAI) deletion. Yang Y, Li DZ. Hemoglobin; 2014 Nov 15; 38(6):431-4. PubMed ID: 25370866 [Abstract] [Full Text] [Related] Page: [Next] [New Search]