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51

Analysis of DNA Haplotypes Suggests a Genetic Predisposition to Trisomy 21 Associated with DNA Sequences on Chromosome 21

Stylianos E. Antonarakis, Smita D. Kittur, Caterina Metaxotou, Paul C. Watkins and Achyut S. Patel

Journal:

Proceedings of the National Academy of Sciences

Year:

1985

Language:

english

File:

PDF, 1.15 MB

english, 1985

52

Haemoglobin Bart's Hydrops Syndrome In Greece

C. Kattamis, A. Metaxotou-Mavromati, E. Tsiarta, C. Metaxatou, P. Wasi, W. G. Wood, L. Pressley, D. R. Higgs, J. B. Clegg and D. J. Weatherall

Journal:

The British Medical Journal

Year:

1980

Language:

english

File:

PDF, 994 KB

english, 1980

53

Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α + -Thalassemia Mutations

Douna, Varvara, Papassotiriou, Ioannis, Metaxotou-Mavrommati, Anna, Stamoulakatou, Alexandra, Liapi, Dimitra, Kampourakis, Dimitrios, Tsilimigaki, Amalia, Kanavakis, Emmanuel, Traeger-Synodinos, Joann

Journal:

Year:

2008

Language:

english

File:

PDF, 107 KB

english, 2008

54

A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α + -Thalassemia Deletion: Clinical Aspects in Two Cases

Douna, Varvara, Papassotiriou, Ioannis, Garoufi, Anastasia, Georgouli, Eleni, Ladis, Vassilis, Stamoulakatou, Alexandra, Metaxotou-Mavrommati, Anna, Kanavakis, Emmanuel, Traeger-Synodinos, Joanne

Journal:

Year:

2008

Language:

english

File:

PDF, 123 KB

english, 2008

55

Interaction of an α + -Thalassemia Deletion with Either a Highly Unstable α-Globin Variant (α2, Codon 59, GGC→GAC) or a Nondeletional α-Thalassemia Mutation (AATAA→AATAAG): Comparison of Phenotypes Illustrating “Dominant” α-Thalassemia

Traeger-Synodinos, J., Metaxotou-Mavrommati, A., Karagiorga, M., Vrettou, C., Papassotiriou, I., Stamoulakatou, A., Kanavakis, E.

Journal:

Year:

1999

Language:

english

File:

PDF, 740 KB

english, 1999

56

An α-Thalassemic Hemoglobinopathy: Homozygosity for the Hb Agrinio α2-Globin Chain Variant

Traeger-Synodinos, J., Metaxotou-Mavromati, A., Kanavakis, E., Vrettou, C., Papassotiriou, I., Michael, Th., Kattamis, C.

Journal:

Year:

1998

Language:

english

File:

PDF, 356 KB

english, 1998

57

Association of Mild and Severely Unstable α Chain Variants: The First Observation of a Compound Heterozygote with Hb Setif [α94(G1)Asp→Tyr (α2)] and Hb Agrinio [α29(B10)Leu→Pro (α2)] in a Greek Family

Douna, Varvara, Papassotiriou, Ioannis, Stamoulakatou, Alexandra, Metaxotou-Mavrommati, Anna, Kanavakis, Emmanuel, Traeger-Synodinos, Joanne

Journal:

Year:

2008

Language:

english

File:

PDF, 79 KB

english, 2008

58

Molecular Studies of β-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.

Journal:

Year:

2000

Language:

english

File:

PDF, 947 KB

english, 2000

59

Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F.

Kattamis, C, Lagos, P, Metaxotou-Mavromati, A, Matsaniotis, N

Journal:

Journal of Medical Genetics

Year:

1972

Language:

english

File:

PDF, 847 KB

english, 1972

60

Correspondence

Kattamis, C., Lagos, P., Metaxotou-Mavromati, A., Matsaniotis, N.

Journal:

Journal of Medical Genetics

Year:

1973

Language:

english

File:

PDF, 110 KB

english, 1973

61

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

Florentin, L, Mavrou, A, Kekou, K, Metaxotou, C

Journal:

Journal of Medical Genetics

Year:

1995

Language:

english

File:

PDF, 597 KB

english, 1995

62

Molecular Characterization of Homozygous (High HbA2) β-Thalassemia Intermedia in Greece

Kanavakis, Emmanuel, Traeger-Synodinos, Joanne, Tzetis, Maria, Metaxotou-Mavromati, Anna, Ladis, Vasilis, Kattamis, Christos

Journal:

Pediatric Hematology-Oncology

Year:

1995

Language:

english

File:

PDF, 561 KB

english, 1995

63

Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia.

Metaxotou-Mavromati, A, Kattamis, C, Matathia, L, Tzetis, M, Kanavakis, E

Journal:

Journal of Medical Genetics

Year:

1988

Language:

english

File:

PDF, 716 KB

english, 1988

64

Identification of Fetal Nucleated Red Blood Cells in the Maternal Circulation during Pregnancy Using Anti-Hemoglobin-&epsi; Antibody

Mavrou, A., Kolialexi, A., Antsaklis, A., Korantzis, A., Metaxotou, C.

Journal:

Fetal Diagnosis and Therapy

Year:

2003

Language:

english

File:

PDF, 95 KB

english, 2003

65

Clinical Response and Adverse Events in Young Patients with Sickle Cell Disease Treated with Hydroxyurea

Kattamis, Antonis, Lagona, Evangelia, Orfanou, Irini, Psichou, Fotini, Ladis, Vasilis, Kanavakis, Emmanuel, Metaxotou-Mavrommati, Anna, Kattamis, Christos

Journal:

Pediatric Hematology-Oncology

Year:

2004

Language:

english

File:

PDF, 304 KB

english, 2004

66

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome

Warren, A., Chakravarti, A, Wong, C, Slaugenhaupt, S., Halloran, S., Watkins, P., Metaxotou, C, Antonarakis, S.

Journal:

Year:

1987

Language:

english

File:

PDF, 766 KB

english, 1987

67

Prevalence of β 0 and β + Thalassemia Genes in Greek Children with Homozygous β-Thalassemia

Kattamis, Christos, Karambula, Katerina, Metaxotou-Mavromati, Anna, Ladis, Vasilios, Constantopoulos, Andreas

Journal:

Year:

1978

Language:

english

File:

PDF, 661 KB

english, 1978

68

Analysis of DNA haplotypes suggests a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21.

Antonarakis, S. E., Kittur, S. D., Metaxotou, C., Watkins, P. C., Patel, A. S.

Journal:

Proceedings of the National Academy of Sciences

Year:

1985

Language:

english

File:

PDF, 961 KB

english, 1985

69

Globin chain synthesis and clinical and hematologic findings in double heterozygotes for the silent and classical ß-thalassemia genes, and their parents

Kattamis, C, Metaxotou-Mavromati, Anna, Wood, W G, Weatherall, D

Journal:

Pediatric Research

Year:

1979

Language:

english

File:

PDF, 151 KB

english, 1979

70

DETECTION OF DONOR'S LYMPHOCYTES IN THE PERIPHERAL BLOOD OF NEONATES FOLLOWING EXCHANGE-TRANSFUSION

Xanthou, M, Mandyla, H, Berietou, M, Metaxotou, C

Journal:

Pediatric Research

Year:

1984

Language:

english

File:

PDF, 151 KB

english, 1984

71

800 ANAIXSIS OF DNA HAPLOTYPES SUGGESTS A GENETIC PREDISPOSITION TO TRISOMY 21 ASSOCIATED WITH DNA SEQUENCES ON CHROMOSOME 21

Antonarakis, S E, Kittur, S D, Metaxotou, C, Patel, A S, Watkins, P E, Kazazian, H H

Journal:

Pediatric Research

Year:

1985

Language:

english

File:

PDF, 173 KB

english, 1985

72

Detection of Nucleated Erythrocytes (NRBC) In Chorionic Villus Sample Supernatant Fluid Using an anti-ε Monoclonal Antibody

Mavrou, A, Kolialexi, A, Kanavakis, E, Vretou, Ch, Metaxotou, C, Bianchi, D W

Journal:

Pediatric Research

Year:

1999

File:

PDF, 70 KB

1999

73

22q11 microdeletion syndrome

Kolialexi, A, Fryssira, H, Mavrou, A, Tziropoulou, M, Metaxotou, C

Journal:

Pediatric Research

Year:

1999

File:

PDF, 70 KB

1999

74

Improved Specificity of NRBC Detection in Chorionic Villus Sample Supernatant Fluids Using Anti-Zeta and Anti-Epsilon Monoclonal Antibodies

Mavrou, Ariadni, Kolialexi, Angeliki, Zheng, Yun-Ling, Metaxotou, Catherine, Bianchi, Diana W.

Journal:

Fetal Diagnosis and Therapy

Year:

1999

Language:

english

File:

PDF, 298 KB

english, 1999

75

Haemoglobin Bart's hydrops syndrome in Greece.

Kattamis, C, Metaxotou-Mavromati, A, Tsiarta, E, Metaxatou, C, Wasi, P, Wood, W G, Pressley, L, Higgs, D R, Clegg, J B, Weatherall, D J

Journal:

Year:

1980

Language:

english

File:

PDF, 964 KB

english, 1980

76

Beta-thalassaemia, G-6-PD deficiency, and atypical cholinesterase in Cyprus.

Kattamis, C, Haidas, S, Metaxotou-Mavromati, A, Matsaniotis, N

Journal:

Year:

1972

Language:

english

File:

PDF, 669 KB

english, 1972