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A Metaxotou-Mavromati

Observed names: A D Metaxotou-Mavromati, A. METAXOTOU‐MAVROMATI, A. Metaxotou-Mavromati, A. Metaxotou‐Mavromati, Anna D. Metaxotou-Mavromati, Anna Metaxotou-Mavromati, Anna Metaxotou‐Mavromati
Observed institutions: Babraham Institute, Siriraj Hospital, National and Kapodistrian University of Athens, University of Cambridge, John Radcliffe Hospital, University of Oxford, Children's Hospital Agia Sophia, MRC Molecular Haematology Unit
OpenAlex ID: A5014134147
The triplicated α‐globin gene locus in β‐thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies
1996 · J. Traeger‐Synodinos, E. Kanavakis, et al. · British Journal of Haematology · 95
The Corfu δβ thalassemia deletion disrupts γ-globin gene silencing and reveals post-transcriptional regulation of HbF expression
2004 · Lyubomira Chakalova, Cameron S. Osborne, et al. · Blood · 80
The triplicated α gene locus and β thalassaemia
1983 · E. Kanavakis, A. Metaxotou‐Mavromati, et al. · British Journal of Haematology · 54
The Heterogeneity of Normal Hb A2‐β Thalassaemia in Greece
1979 · C. Kattamis, A. Metaxotou‐Mavromati, et al. · British Journal of Haematology · 49
Frequency of α‐thalassemia in Greece
1986 · E. Kanavakis, S. Tzotzos, et al. · American Journal of Hematology · 36
Serum iron and unsaturated iron-binding capacity in the -thalassaemia trait: their relation to the levels of haemoglobins A, A 2 , and F.
1972 · C Kattamis, P Lagos, et al. · Journal of Medical Genetics · 35
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A Novel Deletion in the β‐Globin Gene Complex
1985 · J. S. WAINSCOAT, S. L. THEIN, et al. · Annals of the New York Academy of Sciences · 29
The interaction of α° thalassaemia with Hb Icaria: three unusual cases of haemoglobinopathy H
1996 · E. Kanavakis, J. Traeger‐Synodinos, et al. · British Journal of Haematology · 21
The molecular basis of normal HbA2 (type 2) beta-thalassemia in Greece.
1994 · M Tzetis, J Traeger-Synodinos, et al. · PubMed · 21
The clinical phenotype of ? and ?? thalassemias in Greece
1982 · C. Kattamis, A. Metaxotou-Mavromati, et al. · European Journal of Pediatrics · 21
Haemoglobin Bart's hydrops syndrome in Greece.
1980 · C Kattamis, A Metaxotou-Mavromati, et al. · BMJ · 20
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The Corfu δβ thalassaemia mutation in Greece: haematological phenotype and prevalence
1991 · Joanne Traeger‐Synodinos, Maria Tzetis, et al. · British Journal of Haematology · 19
Developmental Changes in Hemoglobin F Levels During the First Two Years of Life in Normal and Heterozygous β-Thalassemia Infants
1982 · Anna D. Metaxotou-Mavromati, Helene K. Antonopoulou, et al. · PEDIATRICS · 18
An α-Thalassemic Hemoglobinopathy: Homozygosity for the Hb Agrinio α2-Globin Chain Variant
1998 · J. Traeger-Synodinos, A. Metaxotou-Mavromati, et al. · Hemoglobin · 15
Prevalence of β0and β+Thalassemia Genes in Greek Children with Homozygous β-Thalassemia
1978 · Christos Kattamis, Katerina Karambula, et al. · Hemoglobin · 15
The Clinical and Haematological Findings in Children Inheriting Two Types of Thalassaemia: High‐A2 Type β‐Thalassaemia, and High‐F Type or δβ‐Thalassaemia
1973 · C. Kattamis, Anna Metaxotou‐Mavromati, et al. · British Journal of Haematology · 14
Molecular Characterization of Homozygous (High HbA2) β-Thalassemia Intermedia in Greece
1995 · Emmanuel Kanavakis, Joanne Traeger-Synodinos, et al. · Pediatric Hematology and Oncology · 13
Developmental changes in hemoglobin F levels during the first two years of life in normal and heterozygous beta-thalassemia infants.
1982 · A D Metaxotou-Mavromati, H K Antonopoulou, et al. · PubMed · 13
Globin gene mapping in normal Hb A2 types of β‐thalassaemia
1982 · E. Kanavakis, A. Metaxotou‐Mavromati, et al. · British Journal of Haematology · 13
Hematologic Phenotype of the Mutations Ivs1-n6 (T →. C), lVS1-n110 (C → A), AND CD39 (C → T) IN CARRIERS OF P-THALASSEMIA IN GREECE
1994 · L. Stefanis, E. Kanavakis, et al. · Pediatric Hematology and Oncology · 12
The molecular basis of HbH disease in Greece
1986 · S. Tzotzos, E. Kanavakis, et al. · British Journal of Haematology · 10
Beta-thalassaemia, G-6-PD deficiency, and atypical cholinesterase in Cyprus.
1972 · C Kattamis, S Haidas, et al. · BMJ · 10
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Clinical, haematological, and genetic studies of type 2 normal Hb A2 beta thalassaemia.
1988 · A Metaxotou-Mavromati, C Kattamis, et al. · Journal of Medical Genetics · 4
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A new ? chain variant hemoglobin A2-Corfu or ?2?2 116 Arg?Cys (G18), detected by ?-globin gene analysis in a Greek family
1991 · Georgios Loudianos, Stefania Murru, et al. · Human Genetics · 3
‘SILENT’β THALASSAEMIA AND NORMAL HbiA2β THALASSAEMIA
1980 · A. Kaltsoya‐Tassiopoulou, N.Z Oumbos, et al. · British Journal of Haematology · 3
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Works count: 34
Citation count: 632
H-index: 15
I10-index: 22
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