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hMSH2 is the most commonly mutated MMR gene in a cohort of Greek HNPCC patients

British journal of cancer, 2005-01, Vol.92 (2), p.396-404

2005

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Abstract P3-03-03: Analysis of hereditary cancer syndromes by use of a panel of genes: More answers than questions

Cancer research (Chicago, Ill.), 2018-02, Vol.78 (4_Supplement), p.P3-P3-03-03

2018

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Abstract P4-03-07: Analysis of hereditary cancer syndromes by using a panel of genes: Novel and multiple pathogenic mutations

Cancer research (Chicago, Ill.), 2019-02, Vol.79 (4_Supplement), p.P4-P4-03-07

2019

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Clinicopathological characteristics and BRCA1/2 mutation rate in male breast cancer: a retrospective case series by the Hellenic Society of Medical Oncology

Annals of oncology, 2016-10, Vol.27, p.vi50-vi50

2016

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Pregnancy following preimplantation genetic diagnosis for Crouzon syndrome

Molecular human reproduction, 2002-03, Vol.8 (3), p.304-309

2002

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First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2)

Prenatal diagnosis, 2002-06, Vol.22 (6), p.519-524

2002

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Genetic alterations of the APC gene in familial adenomatous polyposis patients of the hellenic group for the study of colorectal cancer

Anticancer research, 2003-05, Vol.23 (3A), p.2191

2003

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Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis

Genetics in medicine, 2007-12, Vol.9 (12), p.836-841

2007

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Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer

BMC cancer, 2004-09, Vol.4 (1), p.61-61

2004

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Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR

Prenatal diagnosis, 2002-05, Vol.22 (5), p.360-365

2002

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Ethical Issues Related to Genetic Testing of Families with Hereditary Non-Polyposis Colorectal Cancer and Familial Adenomatosis Polyposis Syndrome

Endoscopy, 2006, Vol.38 (10)

2006

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Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients

BMC cancer, 2005-04, Vol.5 (1), p.40-40, Article 40

2005

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Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders

Prenatal diagnosis, 2002-06, Vol.22 (6), p.525-533

2002

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Elucidation of the Transmission of a Novel Mutation in BRCA1 (1125delCT) in a Family with Multiple Cases of Breast Cancer

Cancer genomics & proteomics, 2009-07, Vol.6 (4), p.215-218

2009

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Different intrafamilial clinical presentation of FMF mutation carriers

Genetic testing, 2008-03, Vol.12 (1), p.125-127

2008

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Evaluation of dHPLC in mutation screening of the APC gene in a Greek FAP cohort

Anticancer research, 2003-05, Vol.23 (3B), p.2691

2003

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O-15. PGD of five single-gene disorders

Reproductive biomedicine online, 2002, Vol.4, p.16-16

2002

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First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2) : Preimplantation Genetics and Diagnosis

Prenatal diagnosis, 2002, Vol.22 (6), p.519-524

2002

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Effect of periodontal therapy on COPD outcomes: a systematic review

BMC pulmonary medicine, 2021-03, Vol.21 (1), p.92-92, Article 92

2021

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Investigation of the relationship between sleep disorders and xerostomia

Clinical oral investigations, 2020-05, Vol.24 (5), p.1709-1716

2020

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Effect of Third Molar Surgery on Sleep Health Parameters of Young Adults: An Observational Study

Medicina (Kaunas, Lithuania), 2024-06, Vol.60 (6), p.858

2024

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Is COPD the Determinant Factor for Myocardial Injury and Cardiac Wall Stress in OSA Patients?

Medicina (Kaunas, Lithuania), 2023-10, Vol.59 (10), p.1759

2023

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Fusion of a maxillary third molar with a supernumerary fourth molar: A case report

Clinical case reports, 2024-02, Vol.12 (2), p.e8484-n/a

2024

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THE EFFECT OF THE SURGICAL EXTRACTION OF MANDIBULAR WISDOM TOOTH IN SLEEP PARAMETERS

Archeia Hellēnikēs stomatikēs & gnathoprosōpikēs cheirourgikēs, 2023-12, Vol.24 (3)

2023

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hMSH2 is the most commonly mutated MMR gene in a cohort of Greek HNPCC patients

Abstract P3-03-03: Analysis of hereditary cancer syndromes by use of a panel of genes: More answers than questions

Abstract P4-03-07: Analysis of hereditary cancer syndromes by using a panel of genes: Novel and multiple pathogenic mutations

Clinicopathological characteristics and BRCA1/2 mutation rate in male breast cancer: a retrospective case series by the Hellenic Society of Medical Oncology

Pregnancy following preimplantation genetic diagnosis for Crouzon syndrome

First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2)

Genetic alterations of the APC gene in familial adenomatous polyposis patients of the hellenic group for the study of colorectal cancer

Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis

Characterization of a novel large deletion and single point mutations in the BRCA1 gene in a Greek cohort of families with suspected hereditary breast cancer

Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR

Ethical Issues Related to Genetic Testing of Families with Hereditary Non-Polyposis Colorectal Cancer and Familial Adenomatosis Polyposis Syndrome

Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients

Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders

Elucidation of the Transmission of a Novel Mutation in BRCA1 (1125delCT) in a Family with Multiple Cases of Breast Cancer

Different intrafamilial clinical presentation of FMF mutation carriers

Evaluation of dHPLC in mutation screening of the APC gene in a Greek FAP cohort

O-15. PGD of five single-gene disorders

First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2) : Preimplantation Genetics and Diagnosis

Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations

Effect of periodontal therapy on COPD outcomes: a systematic review

Investigation of the relationship between sleep disorders and xerostomia

Effect of Third Molar Surgery on Sleep Health Parameters of Young Adults: An Observational Study

Is COPD the Determinant Factor for Myocardial Injury and Cardiac Wall Stress in OSA Patients?

Fusion of a maxillary third molar with a supernumerary fourth molar: A case report

THE EFFECT OF THE SURGICAL EXTRACTION OF MANDIBULAR WISDOM TOOTH IN SLEEP PARAMETERS

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