183 related articles for article (PubMed ID: 14757425)
1. Rare thalassemic syndrome caused by interaction of Hb Questembert (alpha1 codon 131, TCT>CCT, Ser>Pro) with an alpha-thalassemia-2 deletion: implications for diagnosis and management.
Stamoulakatou A; Athanasiou-Metaxa M; Traeger-Synodinos J; Lazaropoulou C; Harteveld K; Premetis E; Tsantali H; Zorai A; Giordano P; Papassotiriou I; Kanavakis E
Blood Cells Mol Dis; 2004; 32(1):118-23. PubMed ID: 14757425
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Interaction of an alpha(+)-thalassemia deletion with either a highly unstable alpha-globin variant (alpha2, codon 59, GGC-->GAC) or a nondeletional alpha-thalassemia mutation (AATAAA-->AATAAG): comparison of phenotypes illustrating "dominant" alpha-thalassemia.
Traeger-Synodinos J; Metaxotou-Mavrommati A; Karagiorga M; Vrettou C; Papassotiriou I; Stamoulakatou A; Kanavakis E
Hemoglobin; 1999 Nov; 23(4):325-37. PubMed ID: 10569721
[TBL] [Abstract][Full Text] [Related]
4. First description in Tunisia of a point mutation at codon 119 (CCT-->TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletion.
Siala H; Ouali F; Messaoud T; Sfar R; Fattoum S
Hemoglobin; 2005; 29(4):263-8. PubMed ID: 16370486
[TBL] [Abstract][Full Text] [Related]
5. α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (
Panyasai S; Phasit A
Hemoglobin; 2020 Jul; 44(4):264-271. PubMed ID: 32727229
[TBL] [Abstract][Full Text] [Related]
6. A rare thalassemic syndrome caused by interaction of Hb Adana [alpha59(E8)Gly-->Asp] with an alpha+-thalassemia deletion: clinical aspects in two cases.
Douna V; Papassotiriou I; Garoufi A; Georgouli E; Ladis V; Stamoulakatou A; Metaxotou-Mavrommati A; Kanavakis E; Traeger-Synodinos J
Hemoglobin; 2008; 32(4):361-9. PubMed ID: 18654886
[TBL] [Abstract][Full Text] [Related]
7. Novel interactions of two α-Hb variants with SEA deletion α
Srivorakun H; Singha K; Fucharoen G; Fucharoen S
Hematology; 2018 Apr; 23(3):187-191. PubMed ID: 28945175
[TBL] [Abstract][Full Text] [Related]
8. Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia.
Wajcman H; Traeger-Synodinos J; Papassotiriou I; Giordano PC; Harteveld CL; Baudin-Creuza V; Old J
Hemoglobin; 2008; 32(4):327-49. PubMed ID: 18654884
[TBL] [Abstract][Full Text] [Related]
9. An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant.
Traeger-Synodinos J; Metaxotou-Mavromati A; Kanavakis E; Vrettou C; Papassotiriou I; Michael T; Kattamis C
Hemoglobin; 1998 May; 22(3):209-15. PubMed ID: 9629496
[TBL] [Abstract][Full Text] [Related]
10. Hb Souli, a 6 bp in-frame deletion on the HBA2 gene (HBA2: c.[41-46delCCTGGG]) leads to α-thalassemia intermedia, when in trans to a single α-globin gene deletion.
Kattamis A; Delaporta P; Fylaktou I; Vrettou C; Kyriakopoulou D; Stamoulakatou A; Papassotiriou I; Kanavakis E; Traeger-Synodinos J
Hemoglobin; 2015; 39(1):55-7. PubMed ID: 25476779
[TBL] [Abstract][Full Text] [Related]
11. Further identification of the hyperunstable alpha-globin chain variant Hb Heraklion [codons 36/37 (-CCC); Pro-->0 (alpha1)] in Greek cases with co-inherited alpha+-thalassemia mutations.
Douna V; Papassotiriou I; Metaxotou-Mavrommati A; Stamoulakatou A; Liapi D; Kampourakis D; Tsilimigaki A; Kanavakis E; Traeger-Synodinos J
Hemoglobin; 2008; 32(4):379-85. PubMed ID: 18654888
[TBL] [Abstract][Full Text] [Related]
12. Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease.
Viprakasit V; Tanphaichitr VS; Veerakul G; Chinchang W; Petrarat S; Pung-Amritt P; Higgs DR
Am J Hematol; 2004 Mar; 75(3):157-63. PubMed ID: 14978697
[TBL] [Abstract][Full Text] [Related]
13. Compound Heterozygosity for an Unstable Novel Hemoglobin Variant, Hb Dongguan [α52(E1)Ser→Cys (T
Chen WD; Ren YX; Wang YJ; Xie WJ; Li J; Xu AP; Ji L
Hemoglobin; 2019; 43(4-5):286-288. PubMed ID: 31650882
[TBL] [Abstract][Full Text] [Related]
14. Hb Questembert is due to a base substitution (T-->C) in codon 131 of the alpha 2-globin gene and has an alpha-thalassemia biosynthetic ratio.
Rochette J; Barnetson R; Thein SL; Varet B; Valensi F
Am J Hematol; 1995 Apr; 48(4):289-90. PubMed ID: 7717382
[No Abstract] [Full Text] [Related]
15. [Analysis of clinical phenotype and genotype of unstable Hemoglobin Rush].
Ge S; Yang B; Yi W; Huang K; Liu H; Huang X; Chu J; Yang Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):15-20. PubMed ID: 28186586
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Complex interaction of Hb Hekinan [alpha27(B8) Glu-Asp] and Hb E [beta26(B8) Glu-Lys] with a deletional alpha-thalassemia 1 in a Thai family.
Fucharoen S; Changtrakun Y; Ratanasiri T; Fucharoen G; Sanchaisuriya K
Eur J Haematol; 2003 May; 70(5):304-9. PubMed ID: 12694166
[TBL] [Abstract][Full Text] [Related]
19. The molecular basis of alpha-thalassemia in Thailand.
Winichagoon P; Fucharoen S; Wasi P
Southeast Asian J Trop Med Public Health; 1992; 23 Suppl 2():7-13. PubMed ID: 1298997
[TBL] [Abstract][Full Text] [Related]
20. Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathies.
Ho PJ; Rochette J; Rees DC; Fisher CA; Huehns ER; Will AM; Thein SL
Hemoglobin; 1996 May; 20(2):103-12. PubMed ID: 8811313
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
