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.
3. Mild hemoglobin H-constant spring disease with β-thalassemia-a case report. Li DZ; Liao C; Zhou JY; Xie XM; Li J Ann Hematol; 2011 Jan; 90(1):123-4. PubMed ID: 20383502 [No Abstract] [Full Text] [Related]
4. Homozygous hemoglobin Tak causes symptomatic secondary polycythemia in a Thai boy. Tanphaichitr VS; Viprakasit V; Veerakul G; Sanpakit K; Tientadakul P J Pediatr Hematol Oncol; 2003 Mar; 25(3):261-5. PubMed ID: 12621249 [TBL] [Abstract][Full Text] [Related]
5. Ultra-rare Hb Regina ( Mallik N; Jamwal M; Sharma R; Singh N; Sharma P; Bansal D; Trehan A; Chhabra S; Das R J Clin Pathol; 2022 Nov; 75(11):791-792. PubMed ID: 35042755 [No Abstract] [Full Text] [Related]
6. A new form of thalassemia intermedia: Compound heterozygous beta thalassemia and hemoglobin Zurich. Yan CLS; Chan NCN; Lam GKS; Ng KY; Cheng CK; Li CK Pediatr Blood Cancer; 2019 Jun; 66(6):e27720. PubMed ID: 30900795 [No Abstract] [Full Text] [Related]
7. Molecular characterization of thalassemia intermedia with homozygous Hb Malay and Hb Malay/HbE in Thai patients. Fucharoen S; Sanchaisuriya K; Fucharoen G; Surapot S Haematologica; 2001 Jun; 86(6):657-8. PubMed ID: 11418377 [No Abstract] [Full Text] [Related]
8. Erythrocytosis in a child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AAG>AAT or AAC)] associated with a Spanish (δβ)(0)-thalassemia. Ropero P; González FA; Cela E; Beléndez C; Pérez B; Seri C; Fontanes E; Villegas A; Díaz-Mediavilla J Hemoglobin; 2013; 37(1):48-55. PubMed ID: 23215953 [TBL] [Abstract][Full Text] [Related]
9. Hemoglobin New York is not a matter in prenatal screening and diagnosis for beta-thalassemia. Li DZ Pediatr Hematol Oncol; 2008 Dec; 25(8):769-71. PubMed ID: 19065444 [No Abstract] [Full Text] [Related]
10. Hematological and molecular characterization of beta-thalassemia/Hb Tak compound heterozygote. Charoenkwan P; Thanarattanakorn P; Chaovaluksakul S; Sittipreechacharn S; Sae-Tang R; Sanguansermsri T Southeast Asian J Trop Med Public Health; 2003 Jun; 34(2):415-9. PubMed ID: 12971573 [TBL] [Abstract][Full Text] [Related]
11. Delta-Beta Thalassaemia in a Pathan Family. Ahmad SQ; Zafar SI; Malik HS; Ahmed S J Coll Physicians Surg Pak; 2017 Nov; 27(11):722-724. PubMed ID: 29132487 [TBL] [Abstract][Full Text] [Related]
12. Compound heterozygous Hb Tak/Hb E causes secondary erythrocytosis in a Thai family. Teawtrakul N; Sirijirachai C; Chansung G; Fucharoen G Hemoglobin; 2010 Jan; 34(2):165-8. PubMed ID: 20353353 [TBL] [Abstract][Full Text] [Related]
13. Symptomatic erythrocytosis associated with a compound heterozygosity for Hb Lepore-Boston-Washington (δ87-β116) and Hb Johnstown [β109(G11)Val→Leu, GTG>TTG]. Inoue S; Oliveira JL; Hoyer JD; Sharman M Hemoglobin; 2012; 36(4):362-70. PubMed ID: 22563907 [TBL] [Abstract][Full Text] [Related]
14. Thalassaemia in pregnancy. Leung TY; Lao TT Best Pract Res Clin Obstet Gynaecol; 2012 Feb; 26(1):37-51. PubMed ID: 22079388 [TBL] [Abstract][Full Text] [Related]
15. Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature. Kalotychou V; Tzanetea R; Konstantopoulos K; Papassotiriou I; Rombos I Hemoglobin; 2010; 34(4):383-8. PubMed ID: 20642336 [TBL] [Abstract][Full Text] [Related]
16. The pitfall of antenatal thalassaemia screening. Lo TK J Obstet Gynaecol; 2017 Jan; 37(1):109-110. PubMed ID: 27750457 [No Abstract] [Full Text] [Related]
17. Sickle cell thalassemia in pregnancy: a case report. Carpani G; Bozzetti P; Cetin I; Tel A; Moroni GA J Matern Fetal Med; 1996; 5(1):28-30. PubMed ID: 8796762 [TBL] [Abstract][Full Text] [Related]
18. A rare association of giant adrenal myelolipoma in a young female double heterozygous for HbD Punjab and β-thalassemia trait. Kumaresan K; Gupta K; Kalra N; Das R Indian J Pathol Microbiol; 2011; 54(3):635-7. PubMed ID: 21934247 [No Abstract] [Full Text] [Related]
19. Hb Hinwil [beta38(C4)Thr-->Asn, ACC>AAC] associated with beta0-thalassemia in a Sicilian child. Cuccia L; Saieva L; Borsellino Z; Marocco MR; Ruffo GB; Riou J; Capra M Hemoglobin; 2008; 32(6):582-7. PubMed ID: 19065336 [TBL] [Abstract][Full Text] [Related]
20. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases. Srivorakun H; Fucharoen G; Sae-Ung N; Sanchaisuriya K; Ratanasiri T; Fucharoen S Eur J Haematol; 2009 Jul; 83(1):57-65. PubMed ID: 19226360 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]