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Results: 1 to 20 of 99

1.

Haemoglobin Noah Mehmet Oeztuerk (alpha(2) delta(2)143 (H21)His-->Tyr: A novel delta-chain variant in the 2,3-DPG binding site.

Bissé E, Schaeffer C, Hovasse A, Preisler-Adams S, Epting T, Baumstark M, Van Dorsselaer A, Horst J, Wieland H.

J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Aug 1;871(1):55-9. doi: 10.1016/j.jchromb.2008.06.055. Epub 2008 Jul 9.

PMID:
18644751
[PubMed - indexed for MEDLINE]
2.

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. doi: 10.1080/03630260802625733.

PMID:
19205974
[PubMed - indexed for MEDLINE]
3.

Hb Rancho Mirage [beta 143(H21)His----Asp]; a variant in the 2,3-DPG binding site showing normal oxygen affinity at physiological pH.

Moo-Penn WF, Hine TK, Johnson MH, Jue DL, Holland S, George S, Pierce AM, Michalski LA, McDonald MJ.

Hemoglobin. 1992;16(1-2):35-44.

PMID:
1634360
[PubMed - indexed for MEDLINE]
4.

Unstable haemoglobin causing haemolytic anaemia: de novo mutation in Sweden identified by PCR.

Landin B, Astrom M.

J Intern Med. 1993 Mar;233(3):299-302.

PMID:
8450301
[PubMed - indexed for MEDLINE]
5.

Hemoglobin Windsor or beta 11 (A8)Val----Asp: a new unstable beta-chain hemoglobin variant producing a hemolytic anemia.

Gilbert AT, Fleming PJ, Sumner DR, Hughes WG, Holland RA, Tibben EA.

Hemoglobin. 1989;13(5):437-53.

PMID:
2599880
[PubMed - indexed for MEDLINE]
6.

Hb Cambridge-MA [β144(HC1)-β146(HC3)Lys-Tyr-His→0 (HBB c.433 A>T)]: a new high oxygen affinity variant.

Oliveira JL, Swanson K, Wendt P, Caughey TD, Hoyer JD.

Hemoglobin. 2010;34(6):565-71. doi: 10.3109/03630269.2010.526921.

PMID:
21077764
[PubMed - indexed for MEDLINE]
7.

Characterization of hemoglobin bassett (alpha94Asp-->Ala), a variant with very low oxygen affinity.

Abdulmalik O, Safo MK, Lerner NB, Ochotorena J, Daikhin E, Lakka V, Santacroce R, Abraham DJ, Asakura T.

Am J Hematol. 2004 Nov;77(3):268-76.

PMID:
15495251
[PubMed - indexed for MEDLINE]
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. doi: 10.3109/03630269.2011.594138.

PMID:
21797708
[PubMed - indexed for MEDLINE]
9.

Hb Grove City [β38(C4)Thr→Ser, ACC>AGC; HBB: c.116C>G]: a new low oxygen affinity β chain variant.

Taliercio RM, Ashton RW, Horwitz L, Swanson KC, Wendt PC, Hoyer JD, Oliveira JL.

Hemoglobin. 2013;37(4):396-403. doi: 10.3109/03630269.2013.789794. Epub 2013 May 7.

PMID:
23651408
[PubMed - indexed for MEDLINE]
10.

A spurious haemoglobin A(1c) result associated with double heterozygote for haemoglobin Raleigh (β1[NA1]Val → Ala) and α(+)-thalassaemia.

Singha K, Fucharoen G, Chaibunruang A, Netnee P, Fucharoen S.

Ann Clin Biochem. 2012 Sep;49(Pt 5):445-9. doi: 10.1258/acb.2012.011234. Epub 2012 Jul 24.

PMID:
22829696
[PubMed - indexed for MEDLINE]
11.

The presurgical management with erythrocytapheresis of a patient with a high-oxygen-affinity, unstable Hb variant (Hb Bryn Mawr).

Larson PJ, Friedman DF, Reilly MP, Kattamis AC, Asakura T, Fortina P, Cohen AR, Kim HC, Manno CS.

Transfusion. 1997 Jul;37(7):703-7.

PMID:
9225933
[PubMed - indexed for MEDLINE]
12.

[A variant hemoglobin found by dissociation of blood glucose from HbA1c on routine physical examination].

Ogawa K, Bando T, Ogawa M, Miyazaki A, Nakanishi T, Shimizu A.

Rinsho Byori. 2003 Jun;51(6):508-15. Japanese.

PMID:
12884736
[PubMed - indexed for MEDLINE]
13.

Two new alpha chain variants: Hb Boghé [alpha58(E7)His-->Gln, alpha2], a variant on the distal histidine, and Hb CHarolles [alpha103(G10)His-Tyr, alpha1].

Lacan P, Francina A, Souillet G, Aubry M, Couprie N, Dementhon L, Becchi M.

Hemoglobin. 1999 Nov;23(4):345-52.

PMID:
10569723
[PubMed - indexed for MEDLINE]
14.

Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr].

Zanella-Cleon I, Préhu C, Joly P, Riou J, Becchi M, Wajcman H, Francina A.

Hemoglobin. 2009;33(3):177-87. doi: 10.1080/03630260903061184.

PMID:
19657831
[PubMed - indexed for MEDLINE]
15.

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
[PubMed - indexed for MEDLINE]
17.

Hb A2-Monreale [delta146(HC3)His-->Arg], a novel delta chain variant detected in west Sicily.

De Angioletti M, Di Girgenti C, Messineo R, Capra M, Carestia C.

Hemoglobin. 2002 Feb;26(1):1-5.

PMID:
11939506
[PubMed - indexed for MEDLINE]
18.

Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype.

Lacerra G, Testa R, De Angioletti M, Schilirò G, Carestia C.

Hemoglobin. 2003 Aug;27(3):149-59.

PMID:
12908799
[PubMed - indexed for MEDLINE]
19.

Hb Sinai-Baltimore or alpha 2 beta (2)18(A15)Val->Gly, a silent, mildly unstable beta chain variant detected by isoelectrofocusing and high performance liquid chromatography.

Pobedimskaya DD, Molchanova TP, Amernick R, Druskin MS, Webber BB, Wilson JB, Huisman TH.

Hemoglobin. 1993 Dec;17(6):505-12.

PMID:
8144351
[PubMed - indexed for MEDLINE]
20.

Hemoglobin Sendagi (beta 42 Phe----Val): a new unstable hemoglobin variant having an amino acid substitution at CD1 of the beta-chain.

Ogata K, Ito T, Okazaki T, Dan K, Nomura T, Nozawa Y, Kajita A.

Hemoglobin. 1986;10(5):469-81.

PMID:
3781864
[PubMed - indexed for MEDLINE]

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