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Molecular, haematological and clinical studies of the −101 C → T substitution of the β‐globin gene promoter in 25 β‐thalassaemia intermedia patients and 45 heterozygotes

British journal of haematology, 1999-12, Vol.107 (4), p.699-706

1999

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Prenatal diagnosis of the thalassaemia syndromes by rapid DNA analytical methods

Molecular human reproduction, 1997-06, Vol.3 (6), p.523-528

1997

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The triplicated α‐globin gene locus in β‐thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies

British journal of haematology, 1996-12, Vol.95 (3), p.467-471

1996

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Molecular, haematological and clinical studies of a silent β‐gene C → G mutation at 6 bp 3′ to the termination codon (+1480 C → G) in twelve Greek families

British journal of haematology, 1998-10, Vol.103 (1), p.45-51

1998

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GILBERT SYNDROME ASSOCIATED WITH β-THALASSEMIA

Pediatric hematology and oncology, 2001, Vol.18 (8), p.477-484

2001

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Molecular Studies of β-Thalassemia Heterozygotes with Raised Hb F Levels

Hemoglobin, 2000-01, Vol.24 (3), p.203-220

2000

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Rare β-Thalassemia Alleles In the Greek and Greek Cypriot Populations

Hemoglobin, 1998, Vol.22 (1), p.89-94

1998

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Molecular, haematological and clinical studies of the -- 101 C (right arrow) T substitution of the (beta -globin) gene promoter in 25 (beta -thalassaemia) intermedia patients and 45

British journal of haematology, 1999-12, Vol.107 (4), p.699

1999

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Molecular, haematological and clinical studies of a silent (beta-gene) C - G mutation at 6bp 3' to the termination codon (+1481 C - G) in twelve Greek families

British journal of haematology, 1998-10, Vol.103 (1), p.45

1998

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CLINICAL AND HEMATOLOGICAL PHENOTYPE IN 9 FAMILIES WITH THE RARE β-GENE C>G MUTATION AT nt POSITION 6 3′ TO THE TERMINATION CODON. 119

Pediatric research, 1997-05, Vol.41 (5), p.768-768

1997

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ASSESSMENT OF THE HEMATOLOGICAL PHENOTYPE IN 34 CARRIERS OF THEβ-THALASSEMIA-101 C>T (SILENT?) MUTATION 111

Pediatric research, 1997-05, Vol.41 (5), p.766-766

1997

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On the properties of H i shells in the Small Magellanic Cloud

Monthly notices of the Royal Astronomical Society, 2005-07, Vol.360 (3), p.1171-1184

2005

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P-086: Total colectomy in pediatric ulcerative colitis: a cohort study from a tertiary center in Greece

Journal of Crohn's and colitis, 2014-09, Vol.8, p.S425-S425

2014

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The recent structural evolution of the SMC

Astronomy and astrophysics (Berlin), 2001-12, Vol.379 (3), p.864-869

2001

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Star-burst regions in the LMC

Astronomy and astrophysics (Berlin), 2006-05, Vol.451 (2), p.431-434

2006

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On the properties of H i shells in the Small Magellanic Cloud

Monthly notices of the Royal Astronomical Society, 2005-07, Vol.360 (3), p.1171-1184

2005

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Automatic Extraction and Classification of Low-Dispersion Objective-Prism Stellar Spectra

Baltic astronomy, 2000, Vol.9 (4), p.541-544

2000

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Chelmos (Aroania): a New European Telescope Site for the 2.3-m Telescope of the National Observatory of Athens

Symposium - International Astronomical Union, 2001, Vol.196, p.160-162

2001

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The Stellar Complexes in the Large Magellanic Cloud

Symposium - International Astronomical Union, 1999, Vol.190, p.452-453

1999

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Detection and structure of stellar complexes in the large magellanic cloud

Astronomical and astrophysical transactions, 1999-12, Vol.18 (3), p.487-492

1999

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Anemias. Hemoglobinopathies
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Molecular, haematological and clinical studies of the −101 C → T substitution of the β‐globin gene promoter in 25 β‐thalassaemia intermedia patients and 45 heterozygotes

Prenatal diagnosis of the thalassaemia syndromes by rapid DNA analytical methods

The triplicated α‐globin gene locus in β‐thalassaemia heterozygotes: clinical, haematological, biosynthetic and molecular studies

Molecular, haematological and clinical studies of a silent β‐gene C → G mutation at 6 bp 3′ to the termination codon (+1480 C → G) in twelve Greek families

GILBERT SYNDROME ASSOCIATED WITH β-THALASSEMIA

Molecular Studies of β-Thalassemia Heterozygotes with Raised Hb F Levels

Rare β-Thalassemia Alleles In the Greek and Greek Cypriot Populations

Molecular, haematological and clinical studies of the -- 101 C (right arrow) T substitution of the (beta -globin) gene promoter in 25 (beta -thalassaemia) intermedia patients and 45

Molecular, haematological and clinical studies of a silent (beta-gene) C - G mutation at 6bp 3' to the termination codon (+1481 C - G) in twelve Greek families

CLINICAL AND HEMATOLOGICAL PHENOTYPE IN 9 FAMILIES WITH THE RARE β-GENE C>G MUTATION AT nt POSITION 6 3′ TO THE TERMINATION CODON. 119

ASSESSMENT OF THE HEMATOLOGICAL PHENOTYPE IN 34 CARRIERS OF THEβ-THALASSEMIA-101 C>T (SILENT?) MUTATION 111

On the properties of H i shells in the Small Magellanic Cloud

P-086: Total colectomy in pediatric ulcerative colitis: a cohort study from a tertiary center in Greece

The recent structural evolution of the SMC

Star-burst regions in the LMC

On the properties of H i shells in the Small Magellanic Cloud

Automatic Extraction and Classification of Low-Dispersion Objective-Prism Stellar Spectra

Chelmos (Aroania): a New European Telescope Site for the 2.3-m Telescope of the National Observatory of Athens

The Stellar Complexes in the Large Magellanic Cloud

Detection and structure of stellar complexes in the large magellanic cloud

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