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.
114 related articles for article (PubMed ID: 20854117)
1. Hb St. Truiden [α68(E17)Asn→His] and Hb Westeinde [α125(H8)Leu→Gln]: two new abnormalities of the α2-globin gene. Kaufmann JO; Phylipsen M; Neven C; Huisman W; van Delft P; Bakker-Verweij M; Arkesteijn SG; Harteveld CL; Giordano PC Hemoglobin; 2010; 34(5):439-44. PubMed ID: 20854117 [TBL] [Abstract][Full Text] [Related]
2. A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chain. Garçon L; Iolascon A; Pissard S; Esposito MR; Russo R; Fenneteau O; Fénéant-Thibault M; Heimpel H; Delaunay J Hemoglobin; 2010; 34(6):576-81. PubMed ID: 21077766 [TBL] [Abstract][Full Text] [Related]
3. A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2). Martin G; Villegas A; González FA; Ropero P; Hojas R; Polo M; Mateo M; Salvador M; Benavente C Hemoglobin; 2005; 29(2):113-7. PubMed ID: 15921163 [TBL] [Abstract][Full Text] [Related]
4. Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype. Harteveld CL; Steen G; Vlasveld LT; van Delft P; Giordano PC Haematologica; 2006 Apr; 91(4):570-1. PubMed ID: 16533721 [TBL] [Abstract][Full Text] [Related]
5. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype. Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225 [TBL] [Abstract][Full Text] [Related]
6. Association of mild and severely unstable alpha chain variants: the first observation of a compound heterozygote with Hb Setif [alpha94(G1)Asp-->Tyr (alpha2)] and Hb Agrinio [alpha29(B10)Leu-->Pro (alpha2)] in a Greek family. Douna V; Papassotiriou I; Stamoulakatou A; Metaxotou-Mavrommati A; Kanavakis E; Traeger-Synodinos J Hemoglobin; 2008; 32(6):592-5. PubMed ID: 19065338 [TBL] [Abstract][Full Text] [Related]
7. Hb Plasencia [α125(H8)Leu→Arg (α2)] is a frequent cause of α+-thalassemia in the Portuguese population. Cunha E; Bento C; Oliveira A; Relvas L; Neves J; Gameiro M; Barros C; Araújo A; Macedo A; Rocha P; Costa R; Maia T; Ribeiro ML Hemoglobin; 2013; 37(2):183-7. PubMed ID: 23368878 [TBL] [Abstract][Full Text] [Related]
8. A new α1-globin mutation, Hb Brugg [α20(B1)His→Gln]. Rizzi M; Zurbriggen K; Schmid M; Goede JS; Nardi MA; Schmugge M; Speer O Hemoglobin; 2011; 35(4):417-22. PubMed ID: 21797708 [TBL] [Abstract][Full Text] [Related]
9. Description of two new alpha variants: Hb Canuts [alpha85(F6)Asp-->His (alpha1)] and Hb Ambroise Pare [alpha117(GH5)Phe-->Ile (alpha2)]; two new beta variants: Hb Beaujolais [beta84(EF8)Thr-->Asn] and Hb Monplaisir [beta147 (Tyr-Lys-Leu-Ala-Phe-Phe-Leu-Leu-Ser-Asn-Phe-Tyr-158-COOH)] and one new delta variant: Hb (A2)North Africa [delta59(E3)Lys-->Met]. Joly P; Lacan P; Bererd M; Garcia C; Zanella-Cleon I; Becchi M; Aubry M; Couprie N; Francina A Hemoglobin; 2009; 33(3):196-205. PubMed ID: 19657833 [TBL] [Abstract][Full Text] [Related]
10. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia. Srivorakun H; Fucharoen G; Puangplruk R; Kheawon N; Fucharoen S Eur J Haematol; 2011 Jul; 87(1):68-72. PubMed ID: 21447006 [TBL] [Abstract][Full Text] [Related]
11. 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; 34(4):354-65. PubMed ID: 20642333 [TBL] [Abstract][Full Text] [Related]
12. Hb Charlieu [alpha106(G13)Leu-->Pro (alpha1)]: a new phenotypically silent hemoglobin variant associated with a mild alpha-thalassemia phenotype. Joly P; Szymanowicz A; Neyron MJ; Zine A; Wajcman H; Francina A Hemoglobin; 2010; 34(4):366-73. PubMed ID: 20642334 [TBL] [Abstract][Full Text] [Related]
13. A new alpha-globin variant with increased oxygen affinity in a Swiss family: Hb Frauenfeld [alpha 138(H21)Ser-->Phe, TCC>TTC (alpha 2)]. Hochuli M; Zurbriggen K; Schmid M; Speer O; Rochat P; Frauchiger B; Kleinert P; Schmugge M; Troxler H Hemoglobin; 2009; 33(1):54-8. PubMed ID: 19205974 [TBL] [Abstract][Full Text] [Related]
14. Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies. Traeger-Synodinos J; Papassotiriou I; Metaxotou-Mavrommati A; Vrettou C; Stamoulakatou A; Kanavakis E Blood Cells Mol Dis; 2000 Aug; 26(4):276-84. PubMed ID: 11042028 [TBL] [Abstract][Full Text] [Related]
15. Complex interaction of Hb E [beta26(B8)Glu-->Lys], Hb Korle-Bu [beta73(E17)Asp-->Asn] and a deletional alpha-thalassemia-1 in pregnancy. Siriratmanawong N; Chansri W; Singsanan S; Fucharoen G; Fucharoen S Hemoglobin; 2009; 33(6):507-14. PubMed ID: 19958198 [TBL] [Abstract][Full Text] [Related]
16. Hb St. Jozef, A Val-->Leu N-terminal mutation leading to retention of the methionine, and partial acetylation found in the globin gene in Cis with a -alpha3.7 thalassemia deletion. Harteveld CL; Versteegh FG; van Leer EH; Starreveld JS; Kok PJ; van Rooijen-Nijdam I; van Delft P; Zanella-Cleon I; Becchi M; Wajcman H; Giordano PC Hemoglobin; 2007; 31(3):313-23. PubMed ID: 17654068 [TBL] [Abstract][Full Text] [Related]
17. Phenotypic variability in a chinese family with nondeletional Hb H-Hb Quong Sze disease. Li J; Liao C; Zhou JY; Xie XM; Li R; Chen LH; Li DZ Hemoglobin; 2011; 35(4):430-3. PubMed ID: 21797711 [TBL] [Abstract][Full Text] [Related]
18. Alpha-thalassemia phenotype induced by the new IVS-II-2 (T --> A) splice donor site mutation on the alpha2-globin gene. Harteveld CL; Jebbink MC; van der Lely N; van Delft P; Akkermans N; Arkesteyn S; Giordano PC Hemoglobin; 2006; 30(1):3-7. PubMed ID: 16540408 [TBL] [Abstract][Full Text] [Related]
20. Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a new α-thalassemic hemoglobin variant found in the Iberian Peninsula: report of six cases. Bento C; Oliveira AC; Neves J; Gameiro M; Cunha E; Coucelo M; Costa RM; Barbot J; Costa E; Fernández-Lago C; Ribeiro ML Hemoglobin; 2012; 36(6):517-25. PubMed ID: 23181747 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]