Traeger-Synodinos J - Search Results

1

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. Wajcman H, et al. Hemoglobin. 2008;32(4):327-49. doi: 10.1080/03630260802173833. Hemoglobin. 2008. PMID: 18654884 Review.

2

Hb Aghia Sophia [alpha62(E11)Val-->0 (alpha1)], an "in-frame" deletion causing alpha-thalassemia.

Traeger-Synodinos J, Harteveld CL, Kanavakis E, Giordano PC, Kattamis C, Bernini LF. Traeger-Synodinos J, et al. Hemoglobin. 1999 Nov;23(4):317-24. doi: 10.3109/03630269909090747. Hemoglobin. 1999. PMID: 10569720

3

Hb Mont Saint Aignan [beta128(H6)Ala-->Pro]: a new unstable variant leading to chronic microcytic anemia.

Wajcman H, Lahary A, Promé D, Kister J, Riou J, Godart C, Préhu C, Traeger-Synodinos J, Papassotiriou I, Galactéros F. Wajcman H, et al. Hemoglobin. 2001 Feb;25(1):57-65. doi: 10.1081/hem-100103070. Hemoglobin. 2001. PMID: 11300350

4

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. Kattamis A, et al. Hemoglobin. 2015;39(1):55-7. doi: 10.3109/03630269.2014.981827. Epub 2014 Dec 5. Hemoglobin. 2015. PMID: 25476779

5

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. Traeger-Synodinos J, et al. Hemoglobin. 1998 May;22(3):209-15. doi: 10.3109/03630269809113135. Hemoglobin. 1998. PMID: 9629496

6

Rapid and accurate quantitation of Hb Bart's and Hb H using weak cation exchange high performance liquid chromatography: correlation with the alpha-thalassemia genotype.

Papassotiriou I, Traeger-Synodinos J, Vlachou C, Karagiorga M, Metaxotou A, Kanavakis E, Stamoulakatou A. Papassotiriou I, et al. Hemoglobin. 1999 Aug;23(3):203-11. doi: 10.3109/03630269909005700. Hemoglobin. 1999. PMID: 10490132

7

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. Traeger-Synodinos J, et al. Hemoglobin. 1999 Nov;23(4):325-37. doi: 10.3109/03630269909090748. Hemoglobin. 1999. PMID: 10569721

8

Molecular studies of beta-thalassemia heterozygotes with raised Hb F levels.

Vrettou C, Kanavakis E, Traeger-Synodinos J, Metaxotou-Mavrommati A, Basiakos I, Maragoudaki E, Stamoulakatou A, Papassotiriou I, Kattamis C. Vrettou C, et al. Hemoglobin. 2000 Aug;24(3):203-20. doi: 10.3109/03630260008997528. Hemoglobin. 2000. PMID: 10975440

9

Hb Sitia [beta128(H6)Ala-->Val]: an unstable variant with a substitution in the alpha1beta1 interface.

Papassotiriou I, Traeger-Synodinos J, Promé D, Kister J, Vrettou C, Xaidara A, Marden M, Stamoulakatou A, Wajcman H, Kanavakis E. Papassotiriou I, et al. Hemoglobin. 2001 Feb;25(1):45-56. doi: 10.1081/hem-100103069. Hemoglobin. 2001. PMID: 11300349

10

Two new beta-thalassemia deletions compromising prenatal diagnosis in an Italian and a Turkish couple seeking prevention.

Phylipsen M, Amato A, Cappabianca MP, Traeger-Synodinos J, Kanavakis E, Basak N, Galanello R, Tuveri T, Ivaldi G, Harteveld CL, Giordano PC. Phylipsen M, et al. Haematologica. 2009 Sep;94(9):1289-92. doi: 10.3324/haematol.2009.007989. Haematologica. 2009. PMID: 19734421 Free PMC article.

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