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Cell-Free Plasma DNA as a Novel Marker of Aseptic Inflammation Severity Related to Exercise Overtraining

Clinical chemistry (Baltimore, Md.), 2006-09, Vol.52 (9), p.1820-1824

2006

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Time of sampling is crucial for measurement of cell-free plasma DNA following acute aseptic inflammation induced by exercise

Clinical biochemistry, 2010-11, Vol.43 (16), p.1368-1370

2010

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Conception and pregnancy outcome in a patient with 11-bp deletion of the steroidogenic acute regulatory protein gene

Fertility and sterility, 2009-03, Vol.91 (3), p.934.e15-934.e18

2009

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Screening human genes for small alterations performing an enzymatic cleavage mismatched analysis (ECMA) protocol

Molecular biotechnology, 2007-11, Vol.37 (3), p.212-219

2007

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Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study

European journal of human genetics : EJHG, 2014-08, Vol.22 (8), p.1012-1018

2014

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Analysis of a founder mutation in the TH gene in a cohort of greek patients with Parkinson's disease

Movement disorders, 2016-11, Vol.31 (11), p.1753-1754

2016

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Single amino acid loss in the dystrophin protein associated with a mild clinical phenotype

Muscle & nerve, 2017-01, Vol.55 (1), p.46-50

2017

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Further delineation of novel 1p36 rearrangements by array-CGH analysis: Narrowing the breakpoints and clarifying the “extended” phenotype

Gene, 2012-09, Vol.506 (2), p.360-368

2012

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Chromosomal Abnormalities in Infertile Greek Men: A Single Institution’s Experience

OBM Genetics, 2023-02, Vol.7 (1), p.1-17

2023

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Wilson Disease in Children: Analysis of 57 Cases

Journal of pediatric gastroenterology and nutrition, 2009-01, Vol.48 (1), p.72-77

2009

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Impaired degradation and aberrant phagocytosis of necrotic cell debris in the peripheral blood of patients with primary Sjögren's syndrome

Journal of autoimmunity, 2015-01, Vol.56, p.12-22

2015

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Microrna expression signatures predict patient progression and disease outcome in pediatric embryonal central nervous system neoplasms

Journal of hematology and oncology, 2014-12, Vol.7 (1), p.96-96, Article 96

2014

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Investigation of FANCA mutations in Greek patients

Anticancer research, 2013-08, Vol.33 (8), p.3369-3374

2013

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Screening Human Genes for Small Alterations Performing an Enzymatic Cleavage Mismatched Analysis (ECMA) Protocol

Molecular biotechnology, 2013-09, Vol.55 (1), p.1-9

2013

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Abnormal DLK1/MEG3 imprinting correlates with decreased HERV-K methylation after assisted reproduction and preimplantation genetic diagnosis

Stress (Amsterdam, Netherlands), 2013-11, Vol.16 (6), p.689-697

2013

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Milroy's primary congenital lymphedema in a male infant and review of the literature

In vivo (Athens), 2010-05, Vol.24 (3), p.309-314

2010

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Author reply

World journal of pediatrics : WJP, 2013-02, Vol.9 (1), p.90-91

2013

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Author reply

World journal of pediatrics : WJP, 2013, Vol.9 (1), p.90-91

2013

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Psychomotor development of children born after preimplantation genetic diagnosis and parental stress evaluation

World journal of pediatrics : WJP, 2012-11, Vol.8 (4), p.309-316

2012

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Cell-free DNA levels in acute myocardial infarction patients during hospitalization

Acta Cardiologica, 2009-02, Vol.64 (1), p.51-57

2009

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SURVEYOR on the Spot: Strengths and Weaknesses in Molecular Diagnostics

The Journal of molecular diagnostics : JMD, 2010-03, Vol.12 (2), p.265-266

2010

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SURVEYOR on the Spot

The Journal of molecular diagnostics : JMD, 2010-03, Vol.12 (2), p.265-266

2010

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A study of a single variant allele (rs1426654) of the pigmentation-related gene SLC24A5 in Greek subjects

Experimental dermatology, 2009-02, Vol.18 (2), p.175-177

2009

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Cystic fibrosis conductance regulator, tumor necrosis factor, interferon alpha-10, interferon alpha-17, and interferon gamma genotyping as potential risk markers in pulmonary sarcoidosis pathogenesis in Greek patients

Genetic testing and molecular biomarkers, 2010-08, Vol.14 (4), p.577-584

2010

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Cell-Free Plasma DNA as a Novel Marker of Aseptic Inflammation Severity Related to Exercise Overtraining

Time of sampling is crucial for measurement of cell-free plasma DNA following acute aseptic inflammation induced by exercise

Conception and pregnancy outcome in a patient with 11-bp deletion of the steroidogenic acute regulatory protein gene

Screening human genes for small alterations performing an enzymatic cleavage mismatched analysis (ECMA) protocol

Evaluation of PCR-based preimplantation genetic diagnosis applied to monogenic diseases: a collaborative ESHRE PGD consortium study

Analysis of a founder mutation in the TH gene in a cohort of greek patients with Parkinson's disease

Single amino acid loss in the dystrophin protein associated with a mild clinical phenotype

Further delineation of novel 1p36 rearrangements by array-CGH analysis: Narrowing the breakpoints and clarifying the “extended” phenotype

Chromosomal Abnormalities in Infertile Greek Men: A Single Institution’s Experience

The complex SNP and CNV genetic architecture of the increased risk of congenital heart defects in Down syndrome

Wilson Disease in Children: Analysis of 57 Cases

Impaired degradation and aberrant phagocytosis of necrotic cell debris in the peripheral blood of patients with primary Sjögren's syndrome

Microrna expression signatures predict patient progression and disease outcome in pediatric embryonal central nervous system neoplasms

Investigation of FANCA mutations in Greek patients

Screening Human Genes for Small Alterations Performing an Enzymatic Cleavage Mismatched Analysis (ECMA) Protocol

Abnormal DLK1/MEG3 imprinting correlates with decreased HERV-K methylation after assisted reproduction and preimplantation genetic diagnosis

Milroy's primary congenital lymphedema in a male infant and review of the literature

Author reply

Author reply

Psychomotor development of children born after preimplantation genetic diagnosis and parental stress evaluation

Cell-free DNA levels in acute myocardial infarction patients during hospitalization

SURVEYOR on the Spot: Strengths and Weaknesses in Molecular Diagnostics

SURVEYOR on the Spot

A study of a single variant allele (rs1426654) of the pigmentation-related gene SLC24A5 in Greek subjects

Cystic fibrosis conductance regulator, tumor necrosis factor, interferon alpha-10, interferon alpha-17, and interferon gamma genotyping as potential risk markers in pulmonary sarcoidosis pathogenesis in Greek patients

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