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An economic analysis of preimplantation genetic testing for aneuploidy by polar body biopsy in advanced maternal age

BJOG : an international journal of obstetrics and gynaecology, 2020-05, Vol.127 (6), p.710-718

2020

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ESHRE PGD Consortium data collection XIII: cycles from January to December 2010 with pregnancy follow-up to October 2011

Human reproduction (Oxford), 2015-08, Vol.30 (8), p.1763-1789

2015

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Blastocyst biopsy versus cleavage stage biopsy and blastocyst transfer for preimplantation genetic diagnosis of β-thalassaemia: a pilot study

Human reproduction (Oxford), 2007-05, Vol.22 (5), p.1443-1449

2007

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The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study

Human reproduction (Oxford), 2018-03, Vol.33 (3), p.520-530

2018

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What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee

Human reproduction (Oxford), 2010-04, Vol.25 (4), p.821-823

2010

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Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD)

Journal of cystic fibrosis, 2016-03, Vol.15 (2), p.163-170

2016

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Scanning of β‐globin gene for identification of β‐thalassemia mutation in Romanian population

Journal of cellular and molecular medicine, 2004-04, Vol.8 (2), p.232-240

2004

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

British journal of haematology, 2000-12, Vol.111 (3), p.915-923

2000

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Rapid and Accurate Quantitation of Hb Bart's and Hb H Using Weak Cation Exchange High Performance Liquid Chromatography: Correlation with the α-Thalassemia Genotype

Hemoglobin, 1999, Vol.23 (3), p.203-211

1999

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Hb MONT SAINT AIGNAN [β128(H6)Ala → Pro]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA

Hemoglobin, 2001-01, Vol.25 (1), p.57-65

2001

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Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome

Genetic testing and molecular biomarkers, 2009-04, Vol.13 (2), p.249-256

2009

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Erythroid bone marrow activity and red cell hemoglobinization in iron sufficient beta-thalassemia heterozygotes as reflected by soluble transferrin receptor and reticulocyte hemoglobin in content. Correlation with genotypes and Hb A(2) levels

Haematologica (Roma), 2003-06, Vol.88 (6), p.631

2003

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The homozygous state for Hb Crete [β129 (H7) Ala→Pro] is associated with a complex phenotype including erythrocytosis and functional anemia

Blood cells, molecules, & diseases, 2005-05, Vol.34 (3), p.229-234

2005

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Birth of a healthy infant following trophectoderm biopsy from blastocysts for PGD of beta-thalassaemia major

Human reproduction (Oxford), 2005-07, Vol.20 (7), p.1855-1859

2005

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Distinct Phenotypic Expression Associated with a New Hyperunstable Alpha Globin Variant (Hb Heraklion, α1cd37(C2)Pro>0): Comparison to Other α-Thalassemic Hemoglobinopathies

Blood cells, molecules, & diseases, 2000-08, Vol.26 (4), p.276-284

2000

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Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene

Haematologica (Roma), 2001-04, Vol.86 (4), p.363

2001

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Correlation of clinical phenotype to genotype in haemoglobin H disease

The Lancet (British edition), 1988-02, Vol.1 (8583), p.442-444

1988

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Mild cystic fibrosis phenotype in patients with the 3272-26A > G mutation

Journal of medical genetics, 1995-05, Vol.32 (5), p.406-407

1995

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Hb Sitia [beta128(H6)Ala-->Val]: an unstable variant with a substitution in the alpha1beta1 interface

Hemoglobin, 2001-02, Vol.25 (1), p.45-56

2001

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Identification of two novel mutations (296 + 1G − C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patients

Molecular and cellular probes, 1995-08, Vol.9 (4), p.283-285

1995

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

British journal of haematology, 1993-11, Vol.85 (3), p.546-552

1993

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Paleopathological findings in radiographs of ancient and modern Greek skulls

Skeletal radiology, 2012-12, Vol.41 (12), p.1605-1611

2012

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An economic analysis of preimplantation genetic testing for aneuploidy by polar body biopsy in advanced maternal age

ESHRE PGD Consortium data collection XIII: cycles from January to December 2010 with pregnancy follow-up to October 2011

Blastocyst biopsy versus cleavage stage biopsy and blastocyst transfer for preimplantation genetic diagnosis of β-thalassaemia: a pilot study

The clinical utility of PGD with HLA matching: a collaborative multi-centre ESHRE study

What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committee

Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD)

Scanning of β‐globin gene for identification of β‐thalassemia mutation in Romanian population

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

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

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

Rapid and Accurate Quantitation of Hb Bart's and Hb H Using Weak Cation Exchange High Performance Liquid Chromatography: Correlation with the α-Thalassemia Genotype

Hb MONT SAINT AIGNAN [β128(H6)Ala → Pro]: A NEW UNSTABLE VARIANT LEADING TO CHRONIC MICROCYTIC ANEMIA

Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome

Erythroid bone marrow activity and red cell hemoglobinization in iron sufficient beta-thalassemia heterozygotes as reflected by soluble transferrin receptor and reticulocyte hemoglobin in content. Correlation with genotypes and Hb A(2) levels

The homozygous state for Hb Crete [β129 (H7) Ala→Pro] is associated with a complex phenotype including erythrocytosis and functional anemia

Birth of a healthy infant following trophectoderm biopsy from blastocysts for PGD of beta-thalassaemia major

Distinct Phenotypic Expression Associated with a New Hyperunstable Alpha Globin Variant (Hb Heraklion, α1cd37(C2)Pro>0): Comparison to Other α-Thalassemic Hemoglobinopathies

Erythroid marrow activity and functional anemia in patients with the rare interaction of a single functional a-globin and beta-globin gene

Correlation of clinical phenotype to genotype in haemoglobin H disease

Mild cystic fibrosis phenotype in patients with the 3272-26A > G mutation

Hb Sitia [beta128(H6)Ala-->Val]: an unstable variant with a substitution in the alpha1beta1 interface

Identification of two novel mutations (296 + 1G − C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patients

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

Paleopathological findings in radiographs of ancient and modern Greek skulls

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