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Items: 1 to 20 of 116

1.

Hb Papanui [α99(G8)Lys→Arg; HBA2: c.299A>G]: a novel silent substitution interfering in Hb A1c determination.

Brennan SO, Chan T.

Hemoglobin. 2013;37(6):589-92. doi: 10.3109/03630269.2013.809734. Epub 2013 Jun 28.

PMID:
23806116
3.

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. doi: 10.3109/03630269.2012.742911.

PMID:
23181747
4.

A novel hemoglobin variant found on the α1 chain: Hb KSVGH (HBA1: p.Lys57_Gly58insSerHisGlySerAlaGlnValLys).

Wang MC, Tsai KW, Chu CH, Yu MS, Lam HC.

Hemoglobin. 2015;39(2):81-7. doi: 10.3109/03630269.2015.1005312. Epub 2015 Feb 11.

PMID:
25669128
5.
6.

Hb G-Waimanalo [A1] [α64(E13)Asp→Asn; HBA1: c.193 G > A] with Decreased Oxygen Affinity.

Karow A, Eekels JJ, Zurbriggen K, Schmid M, Schmugge M, Speer O.

Hemoglobin. 2015;39(6):432-4. doi: 10.3109/03630269.2015.1068798. Epub 2015 Aug 6.

PMID:
26291968
7.

Hb G-Waimanalo [A1] or α64(E13)Asp→Asn (α1) (HBA1: c.193G>A) Observed in a Bulgarian Family.

Petkov G, Dimishkovska M, Tsoneva Ivanova V, Yordanov G, Zdraveski A, Plaseska-Karanfilska D.

Hemoglobin. 2015;39(6):430-1. doi: 10.3109/03630269.2015.1066685. Epub 2015 Jul 27.

PMID:
26212674
8.

Molecular and hematological characteristics of a novel form of α-globin gene triplication: the hemoglobin St.Luke's-Thailand [α95(G2)Pro→Arg] or Hb St. Luke's [A2] HBA2.

Singha K, Fucharoen G, Jetsrisuparb A, Fucharoen S.

Clin Biochem. 2013 May;46(7-8):675-80. doi: 10.1016/j.clinbiochem.2013.01.022. Epub 2013 Feb 5.

PMID:
23395770
9.

A Novel Heme Pocket Hemoglobin Variant Associated with Normal Hematology: Hb Zara or α91(FG3)Leu→Ile (α2) (HBA2: c.274C > A).

Trova S, Mereu P, Decandia L, Cocco E, Masala B, Manca L, Pirastru M.

Hemoglobin. 2015;39(6):427-9. doi: 10.3109/03630269.2015.1071270. Epub 2015 Aug 13.

PMID:
26291971
10.

[Hb Burgos (α1 CD64(E13)(Asp→Asn)): a new hemoglobin variant detected during follow-up of diabetic patients].

de la Fuente-Gonzalo F, Martínez Nieto J, Torrejón MJ, Mayor LA, Velasco D, González Fernández FA, Ropero Gradilla P.

Med Clin (Barc). 2015 Jan 6;144(1):26-9. doi: 10.1016/j.medcli.2014.07.035. Epub 2014 Nov 12. Spanish.

PMID:
25458507
11.

Two new hemoglobin variants: Hb Tallahassee [α3(A1)Ser→Tyr; HBA2: c.11C>A] and Hb madison-NC [β119(GH2)Gly→Ser; HBB: c.358G>A].

Kutlar F, Unguru Y, Dixon N, Patel N, Bailey L, Zhuang L, Carmichael H, Kutlar A.

Hemoglobin. 2014;38(3):207-10. doi: 10.3109/03630269.2014.881371. Epub 2014 Jan 29.

PMID:
24471829
12.

Hb Stanleyville II [alpha 78(EF7) Asn→Lys] occurrence in combination with Hb Constant Spring.

Lin M, Huang Y, Yang LY, Wang Q, Zheng L.

Blood Cells Mol Dis. 2011 Feb 15;46(2):145-6. doi: 10.1016/j.bcmd.2010.10.004. Epub 2010 Nov 18. No abstract available.

PMID:
21093326
13.

Hb Lake Tapawingo [α46(CE4)Phe→Ser; HBA2:c.140T>C]: a new unstable α chain hemoglobin variant associated with low systemic arterial saturation.

Guest EM, Neville KA, Hoyer JD, Safo MK, Garg U, Saunders CJ, Abdulmalik O, Zwick DL.

Hemoglobin. 2011;35(4):411-6. doi: 10.3109/03630269.2011.598986.

14.

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. doi: 10.3109/03630269.2013.763822. Epub 2013 Jan 31.

PMID:
23368878
15.

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. doi: 10.3109/03630269.2010.526922.

PMID:
21077766
16.

Hb taradale [beta82(EF6)Lys-->Arg]: a novel mutation at a 2,3-diphosphoglycerate binding site.

Brennan SO, Sheen C, Chan T, George PM.

Hemoglobin. 2005;29(4):281-4.

PMID:
16370489
17.

Hemoglobin Raleigh as the cause of a falsely increased hemoglobin A1C in an automated ion-exchange HPLC method.

Chen D, Crimmins DL, Hsu FF, Lindberg FP, Scott MG.

Clin Chem. 1998 Jun;44(6 Pt 1):1296-301.

18.

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. doi: 10.1111/j.1600-0609.2011.01616.x.

PMID:
21447006
20.

Hb Ullevaal [β78(EF2)Leu→Val; HBB: c.235C>G], a new hemoglobin variant interfering with Hb A1c measurement using a cation exchange high performance liquid chromatography method.

Grimholt RM, Sudmann ÅA, Piehler AP, Urdal P, Klingenberg O.

Hemoglobin. 2014;38(2):130-2. doi: 10.3109/03630269.2013.858640. Epub 2013 Nov 25.

PMID:
24274186
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