220 related articles for article (PubMed ID: 22428534)
1. First detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in an Italian child.
Paglietti ME; Sollaino MC; Loi D; Barella S; Desogus MF; Galanello R
Hemoglobin; 2012; 36(3):299-304. PubMed ID: 22428534
[TBL] [Abstract][Full Text] [Related]
2. Hb TAYBE: clinical and morphological findings IN 43 patients.
Koren A; Levin C; Zalman L; Palmor H; Filon D; Chubar E; Resnitzky P; Bennett M
Eur J Haematol; 2016 Aug; 97(2):137-44. PubMed ID: 26519868
[TBL] [Abstract][Full Text] [Related]
3. Thrombosis in Hb Taybe [codons 38/39 (-ACC) (α1)].
Juul MB; Vestergaard H; Petersen J; Frederiksen H
Hemoglobin; 2012; 36(6):600-4. PubMed ID: 23181750
[TBL] [Abstract][Full Text] [Related]
4. First observation of Hb Taybe [Codons 38/39 (-Acc) Thr-->0 (alpha1)] in Greece: clinical and hematological findings in patients with co-inherited alpha+-thalassemia mutations.
Douna V; Liapi D; Kampourakis D; Repapinou Z; Papassotiriou I; Stamoulakatou A; Poziopoulos C; Kanavakis E; Traeger-Synodinos J
Hemoglobin; 2008; 32(4):371-8. PubMed ID: 18654887
[TBL] [Abstract][Full Text] [Related]
5. Hb Taybe (alpha 38 or 39 THR deleted): an alpha-globin defect, silent in the heterozygous state and producing severe hemolytic anemia in the homozygous.
Galacteros F; Girodon E; M'Rad A; Martin J; Goossens M; Jaber L; Cohen IJ; Tamary H; Goshen Y; Zaizov R
C R Acad Sci III; 1994 May; 317(5):437-44. PubMed ID: 7994622
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb Sallanches.
Warang P; Nair S; Nadkarni A; Ghosh K; Colah RB
Hemoglobin; 2010; 34(1):45-8. PubMed ID: 20113287
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A combination of two novel alpha globin variants Hb Bridlington (HBA1) and Hb Taybe (HBA2) resulting in severe hemolysis, pulmonary hypertension, and death.
Hill QA; Farrar L; Lordan J; Gallienne A; Henderson S
Hematology; 2015 Jan; 20(1):50-2. PubMed ID: 24716903
[TBL] [Abstract][Full Text] [Related]
11. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
Viprakasit V; Ekwattanakit S; Chalaow N; Riolueang S; Wijit S; Tanyut P; Chat-Uthai N; Tachavanich K
Acta Haematol; 2014; 131(2):88-94. PubMed ID: 24081251
[TBL] [Abstract][Full Text] [Related]
12. Dominantly Inherited beta-Thalassemia.
Efremov GD
Hemoglobin; 2007; 31(2):193-207. PubMed ID: 17486503
[TBL] [Abstract][Full Text] [Related]
13. Hb Gerland [alpha 55(E4)Val-->Ala]: a mutation found on the alpha1-globin gene.
Moradkhani K; Riou J; Francina A; Wajcman H; Prehu C
Hemoglobin; 2008; 32(5):478-84. PubMed ID: 18932073
[TBL] [Abstract][Full Text] [Related]
14. Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia.
Pobedimskaya DD; Molchanova TP; Streichman S; Huisman TH
Am J Hematol; 1994 Nov; 47(3):198-202. PubMed ID: 7942784
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α(0)-thalassemia: molecular and hematological features and differential diagnosis.
Singha K; Srivorakun H; Fucharoen G; Changtrakul Y; Komwilaisak P; Jetsrisuparb A; Puangplruk R; Fucharoen S
Hemoglobin; 2013; 37(1):37-47. PubMed ID: 23215800
[TBL] [Abstract][Full Text] [Related]
20. A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease.
Farashi S; Faramarzi Garous N; Zeinali F; Vakili S; Ashki M; Imanian H; Najmabadi H; Azarkeivan A; Tamaddoni A
Hemoglobin; 2015; 39(3):196-200. PubMed ID: 25976776
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
