Traeger-Synodinos J - Search Results

1

A minimal set of SNPs for the noninvasive prenatal diagnosis of β-thalassaemia.

Papasavva TE, Lederer CW, Traeger-Synodinos J, Mavrou A, Kanavakis E, Ioannou C, Makariou C, Kleanthous M. Papasavva TE, et al. Ann Hum Genet. 2013 Mar;77(2):115-24. doi: 10.1111/ahg.12004. Epub 2013 Jan 31. Ann Hum Genet. 2013. PMID: 23362932

2

The Corfu delta beta thalassaemia mutation in Greece: haematological phenotype and prevalence.

Traeger-Synodinos J, Tzetis M, Kanavakis E, Metaxotou-Mavromati A, Kattamis C. Traeger-Synodinos J, et al. Br J Haematol. 1991 Oct;79(2):302-5. doi: 10.1111/j.1365-2141.1991.tb04537.x. Br J Haematol. 1991. PMID: 1720325

3

Hematologic phenotype of the mutations IVS1-n6 (T-->C), IVS1-n110 (G-->A), and CD39 (C-->T) in carriers of beta-thalassemia in Greece.

Stefanis L, Kanavakis E, Traeger-Synodinos J, Tzetis M, Metaxotou-Mavromati A, Kattamis C. Stefanis L, et al. Pediatr Hematol Oncol. 1994 Sep-Oct;11(5):509-17. doi: 10.3109/08880019409141689. Pediatr Hematol Oncol. 1994. PMID: 7530030

4

Mutation analysis of ten exons of the CFTR gene in Greek cystic fibrosis patients: characterization of 74.5% of CF alleles including one novel mutation.

Kanavakis E, Tzetis M, Antoniadi T, Traeger-Synodinos J, Doudounakis S, Adam G, Matsaniotis N, Kattamis C. Kanavakis E, et al. Hum Genet. 1995 Sep;96(3):364-6. doi: 10.1007/BF00210426. Hum Genet. 1995. PMID: 7544320

5

Molecular characterization of homozygous (high HbA2) beta-thalassemia intermedia in Greece.

Kanavakis E, Traeger-Synodinos J, Tzetis M, Metaxotou-Mavromati A, Ladis V, Kattamis C. Kanavakis E, et al. Pediatr Hematol Oncol. 1995 Jan-Feb;12(1):37-45. doi: 10.3109/08880019509029526. Pediatr Hematol Oncol. 1995. PMID: 7703040

6

Preliminary mutation analysis in the phenylalanine hydroxylase gene in Greek PKU and HPA patients.

Traeger-Synodinos J, Kanavakis E, Kalogerakou M, Soulpi K, Missiou-Tsangaraki S, Kattamis C. Traeger-Synodinos J, et al. Hum Genet. 1994 Nov;94(5):573-5. doi: 10.1007/BF00211031. Hum Genet. 1994. PMID: 7959699

7

The molecular basis of normal HbA2 (type 2) beta-thalassemia in Greece.

Tzetis M, Traeger-Synodinos J, Kanavakis E, Metaxotou-Mavromati A, Kattamis C. Tzetis M, et al. Hematol Pathol. 1994;8(1-2):25-34. Hematol Pathol. 1994. PMID: 8034555

8

A base substitution (T-->C) in codon 29 of the alpha 2-globin gene causes alpha thalassaemia.

Hall GW, Thein SL, Newland AC, Chisholm M, Traeger-Synodinos J, Kanavakis E, Kattamis C, Higgs DR. Hall GW, et al. Br J Haematol. 1993 Nov;85(3):546-52. doi: 10.1111/j.1365-2141.1993.tb03346.x. Br J Haematol. 1993. PMID: 8136277

9

The triplicated alpha-globin gene locus in beta-thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies.

Traeger-Synodinos J, Kanavakis E, Vrettou C, Maragoudaki E, Michael T, Metaxotou-Mavromati A, Kattamis C. Traeger-Synodinos J, et al. Br J Haematol. 1996 Dec;95(3):467-71. doi: 10.1046/j.1365-2141.1996.d01-1939.x. Br J Haematol. 1996. PMID: 8943886

10

A high incidence of mutations in exon 6 of the low-density lipoprotein receptor gene in Greek familial hypercholesterolemia patients, including a novel mutation.

Mavroidis N, Traeger-Synodinos J, Kanavakis E, Drogari E, Matsaniotis N, Humphries SE, Day IN, Kattamis C. Mavroidis N, et al. Hum Mutat. 1997;9(3):274-6. doi: 10.1002/(SICI)1098-1004(1997)9:3<274::AID-HUMU10>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9090532 No abstract available.

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