Karagiorga M - Search Results

1

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. Among authors: karagiorga m. Hemoglobin. 1999 Nov;23(4):325-37. doi: 10.3109/03630269909090748. Hemoglobin. 1999. PMID: 10569721

2

Erythroid marrow activity and hemoglobin H levels in hemoglobin H disease.

Papassotiriou I, Traeger-Synodinos J, Kanavakis E, Karagiorga M, Stamoulakatou A, Kattamis C. Papassotiriou I, et al. Among authors: karagiorga m. J Pediatr Hematol Oncol. 1998 Nov-Dec;20(6):539-44. J Pediatr Hematol Oncol. 1998. PMID: 9856674

3

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. Among authors: karagiorga m. Hemoglobin. 1999 Aug;23(3):203-11. doi: 10.3109/03630269909005700. Hemoglobin. 1999. PMID: 10490132

4

Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience.

Kanavakis E, Papassotiriou I, Karagiorga M, Vrettou C, Metaxotou-Mavrommati A, Stamoulakatou A, Kattamis C, Traeger-Synodinos J. Kanavakis E, et al. Among authors: karagiorga m. Br J Haematol. 2000 Dec;111(3):915-23. Br J Haematol. 2000. PMID: 11122156 Free article.

5

Unusual phenotypic observations associated with a rare HbH disease genotype (- -Med/alphaTSaudialpha): implications for clinical management.

Traeger-Synodinos J, Papassotiriou I, Karagiorga M, Premetis E, Kanavakis E, Stamoulakatou A. Traeger-Synodinos J, et al. Among authors: karagiorga m. Br J Haematol. 2002 Oct;119(1):265-7. doi: 10.1046/j.1365-2141.2002.03777.x. Br J Haematol. 2002. PMID: 12358934 Free article.

6

A novel α(0) -thalassemia deletion in a Greek patient with HbH disease and β-thalassemia trait.

Phylipsen M, Traeger-Synodinos J, van der Kraan M, van Delft P, Bakker G, Geerts M, Kanavakis E, Stamoulakatou A, Karagiorga M, Giordano PC, Harteveld CL. Phylipsen M, et al. Among authors: karagiorga m. Eur J Haematol. 2012 Apr;88(4):356-62. doi: 10.1111/j.1600-0609.2012.01748.x. Epub 2012 Feb 11. Eur J Haematol. 2012. PMID: 22324317

7

Iron overload, cardiac and other factors affecting pregnancy in thalassemia major.

Tsironi M, Karagiorga M, Aessopos A. Tsironi M, et al. Among authors: karagiorga m. Hemoglobin. 2010 Jun;34(3):240-50. doi: 10.3109/03630269.2010.485004. Hemoglobin. 2010. PMID: 20524814

8

Elevated plasma chemokine CCL18/PARC in beta-thalassemia.

Dimitriou E, Verhoek M, Altun S, Karabatsos F, Moraitou M, Youssef J, Boot R, Sarafidou J, Karagiorga M, Aerts H, Michelakakis H. Dimitriou E, et al. Among authors: karagiorga m. Blood Cells Mol Dis. 2005 Nov-Dec;35(3):328-31. doi: 10.1016/j.bcmd.2005.07.006. Epub 2005 Aug 31. Blood Cells Mol Dis. 2005. PMID: 16137900

9

Angioid streaks in homozygous beta thalassemia.

Aessopos A, Stamatelos G, Savvides P, Kavouklis E, Gabriel L, Rombos I, Karagiorga M, Kaklamanis P. Aessopos A, et al. Among authors: karagiorga m. Am J Ophthalmol. 1989 Oct 15;108(4):356-9. doi: 10.1016/s0002-9394(14)73300-8. Am J Ophthalmol. 1989. PMID: 2801854

10

Neutrophil elastase in patients with homozygous beta-thalassemia and pseudoxanthoma elasticum-like syndrome.

Samarkos M, Aessopos A, Fragodimitri C, Karagiorga M, Kalotychou V, Voskaridou E, Kavouklis E, Loukopoulos D. Samarkos M, et al. Among authors: karagiorga m. Am J Hematol. 2000 Feb;63(2):63-7. doi: 10.1002/(sici)1096-8652(200002)63:2<63::aid-ajh1>3.0.co;2-4. Am J Hematol. 2000. PMID: 10629570 Free article. Clinical Trial.

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