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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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Prenatal and preimplantation diagnosis of hemoglobinopathies

International journal of laboratory hematology, 2018-05, Vol.40 (S1), p.74-82

2018

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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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Nablus mask‐like facial syndrome: Report of an atypical case with 8q21.3–q22.1 deletion

American journal of medical genetics. Part A, 2024-07, p.e63826

2024

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The ESHRE PGD Consortium: 10 years of data collection

Human reproduction update, 2012-05, Vol.18 (3), p.234-247

2012

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Aneuploidy in oocytes from women of advanced maternal age: analysis of the causal meiotic errors and impact on embryo development

Human reproduction (Oxford), 2023-12, Vol.38 (12), p.2526-2535

2023

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Preimplantation genetic diagnosis, an alternative to conventional prenatal diagnosis of the hemoglobinopathies

International journal of laboratory hematology, 2013-12, Vol.35 (6), p.571-579

Traeger-Synodinos, J.

2013

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ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010

Human reproduction (Oxford), 2014-05, Vol.29 (5), p.880-903

2014

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ESHRE PGD consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008

Human reproduction (Oxford), 2010-11, Vol.25 (11), p.2685-2707

2010

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ESHRE PGD Consortium data collection IX: cycles from January to December 2006 with pregnancy follow-up to October 2007

Human reproduction (Oxford), 2009-08, Vol.24 (8), p.1786-1810

2009

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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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ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006

Human reproduction (Oxford), 2008-12, Vol.23 (12), p.2629-2645

2008

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Diagnosis and molecular characterization of a novel α 0 -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

International journal of laboratory hematology, 2017-10, Vol.39 (5), p.e124

2017

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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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Preimplantation genetic diagnosis in clinical practice

Journal of medical genetics, 2002-01, Vol.39 (1), p.6-11

2002

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Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high-risk individuals

Clinical genetics, 2003-05, Vol.63 (5), p.400-409

2003

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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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Severe hypertriglyceridaemia in diabetic ketoacidosis: clinical and genetic study

Diabetic medicine, 2004-04, Vol.21 (4), p.380-382

2004

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Aneuploidy in Oocytes From Women of Advanced Maternal Age: Analysis of the Causal Meiotic Errors and Impact on Embryo Development

Obstetrical & gynecological survey, 2024-03, Vol.79 (3), p.164-165

2024

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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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An evaluation of PGD in clinical genetic services through 3 years application for prevention of β‐thalassaemia major and sickle cell thalassaemia

Molecular human reproduction, 2003-05, Vol.9 (5), p.301-307

2003

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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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PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol

Reproductive biomedicine online, 2009, Vol.19 (3), p.418-425

2009

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Pregnancies following blastocyst stage transfer in PGD cycles at risk for β-thalassaemic haemoglobinopathies

Human reproduction (Oxford), 2002-01, Vol.17 (1), p.25-31

2002

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

Prenatal and preimplantation diagnosis of hemoglobinopathies

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

Nablus mask‐like facial syndrome: Report of an atypical case with 8q21.3–q22.1 deletion

The ESHRE PGD Consortium: 10 years of data collection

Aneuploidy in oocytes from women of advanced maternal age: analysis of the causal meiotic errors and impact on embryo development

Preimplantation genetic diagnosis, an alternative to conventional prenatal diagnosis of the hemoglobinopathies

ESHRE PGD Consortium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010

ESHRE PGD consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008

ESHRE PGD Consortium data collection IX: cycles from January to December 2006 with pregnancy follow-up to October 2007

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

ESHRE PGD Consortium data collection VIII: cycles from January to December 2005 with pregnancy follow-up to October 2006

P135: THE CLINGEN HEMOGLOBINOPATHY VARIANT CURATION EXPERT PANEL

Diagnosis and molecular characterization of a novel α 0 -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

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

Preimplantation genetic diagnosis in clinical practice

Cystic fibrosis in Greece: molecular diagnosis, haplotypes, prenatal diagnosis and carrier identification amongst high-risk individuals

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

Severe hypertriglyceridaemia in diabetic ketoacidosis: clinical and genetic study

Aneuploidy in Oocytes From Women of Advanced Maternal Age: Analysis of the Causal Meiotic Errors and Impact on Embryo Development

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

An evaluation of PGD in clinical genetic services through 3 years application for prevention of β‐thalassaemia major and sickle cell thalassaemia

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

PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol

Pregnancies following blastocyst stage transfer in PGD cycles at risk for β-thalassaemic haemoglobinopathies

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