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A novel de novo paracentric inversion [inv(20)(q13.1q13.3)] accompanied by an 11q14.3-q21 microdeletion in a pediatric patient with an intellectual disability

Balkan journal of medical genetics, 2018-12, Vol.21 (2), p.63-67

2018

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Effect of Infant Formula Containing a Low Dose of the Probiotic Bifidobacterium lactis CNCM I-3446 on Immune and Gut Functions in C-Section Delivered Babies: A Pilot Study

Clinical Medicine Insights: Pediatrics, 2016-01, Vol.2016 (2016), p.11-19

2016

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Oral L-arginine supplementation and faecal calprotectin levels in very low birth weight neonates

Journal of perinatology, 2013-02, Vol.33 (2), p.141-146

2013

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C024 Association of NQO1 C609T polymorphism with chromosomes 5 and/or 7 abnormalities in patients with MDS/AML

Leukemia research, 2009-05, Vol.33, p.S45-S46

2009

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A Rare Familial Paracentric Inversion in the Long Arm of Chromosome 8: Case Report and Review of the Literature

Journal of Genetic Disorders & Genetic Reports, 2017, Vol.6 (2)

2017

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Comparison of Bacterial Community Composition of Primary and Persistent Endodontic Infections Using Pyrosequencing

Journal of endodontics, 2015-08, Vol.41 (8), p.1226-1233

2015

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Cohesin RAD21 Gene Promoter Methylation in Patients with Acute Myeloid Leukemia

Life (Basel, Switzerland), 2024-10, Vol.14 (10), p.1311

2024

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The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems

Cytogenetic and genome research, 2023, Vol.163 (5-6), p.274-278

2023

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A new highly sensitive and specific overnight combined screening and diagnostic test for primary aldosteronism

European journal of endocrinology, 2016-07, Vol.175 (1), p.21-28

2016

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I-131 Postablation SPECT/CT Predicts Relapse of Papillary Thyroid Carcinoma more Accurately than Whole Body Scan

In vivo (Athens), 2019-11, Vol.33 (6), p.2255-2263

2019

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Female Reproductive Ageing and Chromosomal Abnormalities in a Large Series of Women Undergoing IVF

Cytogenetic and genome research, 2021, Vol.161 (12), p.551-555

2021

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A 46,XX karyotype in men with infertility: Two new cases and review of the literature

Journal of human reproductive sciences, 2022-07, Vol.15 (3), p.307-317

2022

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Cytogenetic findings of ectopic endometriotic tissue in women with endometriosis and review of the literature

European journal of obstetrics & gynecology and reproductive biology, 2021-09, Vol.264, p.212-218

2021

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Detection of a novel unbalanced X;21 translocation in a girl with Turner syndrome phenotype

Gynecological endocrinology, 2021-04, Vol.37 (4), p.377-381

2021

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Cohesin RAD21 Gene Promoter Methylation in Patients with Chronic Lymphocytic Leukemia

Cytogenetic and genome research, 2018, Vol.154 (3), p.126-131

2018

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Paraoxonase 1 (PON1) Q192R and L55M Polymorphisms as Potential Predisposition Factors for Chronic Lymphocytic Leukemia

Anticancer research, 2019-06, Vol.39 (6), p.2861-2869

2019

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Perinatal lipocalin-2 profile at the extremes of fetal growth

The journal of maternal-fetal & neonatal medicine, 2021-07, Vol.34 (13), p.2166-2172

2021

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Prognostic Significance of VEGF Expression Evaluated by Quantitative Immunohistochemical Analysis in Colorectal Cancer

The Journal of surgical research, 2008-06, Vol.147 (1), p.99-107

2008

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Low-level X Chromosome Mosaicism: A Common Finding in Women Undergoing IVF

In vivo (Athens), 2020-05, Vol.34 (3), p.1433-1437

2020

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Enteral L-Arginine Supplementation for Prevention of Necrotizing Enterocolitis in Very Low Birth Weight Neonates: A Double-Blind Randomized Pilot Study of Efficacy and Safety

JPEN. Journal of parenteral and enteral nutrition, 2013-09, Vol.37 (5), p.617-622

2013

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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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GSTP1 and CYP2B6 Genetic Polymorphisms and the Risk of Bronchopulmonary Dysplasia in Preterm Neonates

American journal of perinatology, 2017-07, Vol.34 (8), p.729-734

2017

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Possible Implication of GSTP1 and NQO1 Polymorphisms on Natalizumab Response in Multiple Sclerosis

Annals of clinical and laboratory science, 2016-12, Vol.46 (6), p.586-591

2016

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Inducible nitric oxide synthase expression and its prognostic significance in colorectal cancer

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 2010-02, Vol.118 (2), p.115-124

2010

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The G⁵¹⁶T CYP2B6 germline polymorphism affects the risk of acute myeloid leukemia and is associated with specific chromosomal abnormalities

PloS one, 2014, Vol.9 (2), p.e88879-e88879

2014

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A novel de novo paracentric inversion [inv(20)(q13.1q13.3)] accompanied by an 11q14.3-q21 microdeletion in a pediatric patient with an intellectual disability

Effect of Infant Formula Containing a Low Dose of the Probiotic Bifidobacterium lactis CNCM I-3446 on Immune and Gut Functions in C-Section Delivered Babies: A Pilot Study

Oral L-arginine supplementation and faecal calprotectin levels in very low birth weight neonates

C024 Association of NQO1 C609T polymorphism with chromosomes 5 and/or 7 abnormalities in patients with MDS/AML

A Rare Familial Paracentric Inversion in the Long Arm of Chromosome 8: Case Report and Review of the Literature

Comparison of Bacterial Community Composition of Primary and Persistent Endodontic Infections Using Pyrosequencing

Cohesin RAD21 Gene Promoter Methylation in Patients with Acute Myeloid Leukemia

The Types and Frequencies of X Chromosome Abnormalities in Women with Reproductive Problems

A new highly sensitive and specific overnight combined screening and diagnostic test for primary aldosteronism

I-131 Postablation SPECT/CT Predicts Relapse of Papillary Thyroid Carcinoma more Accurately than Whole Body Scan

Female Reproductive Ageing and Chromosomal Abnormalities in a Large Series of Women Undergoing IVF

A 46,XX karyotype in men with infertility: Two new cases and review of the literature

Cytogenetic findings of ectopic endometriotic tissue in women with endometriosis and review of the literature

Detection of a novel unbalanced X;21 translocation in a girl with Turner syndrome phenotype

Cohesin RAD21 Gene Promoter Methylation in Patients with Chronic Lymphocytic Leukemia

Paraoxonase 1 (PON1) Q192R and L55M Polymorphisms as Potential Predisposition Factors for Chronic Lymphocytic Leukemia

Perinatal lipocalin-2 profile at the extremes of fetal growth

Prognostic Significance of VEGF Expression Evaluated by Quantitative Immunohistochemical Analysis in Colorectal Cancer

Low-level X Chromosome Mosaicism: A Common Finding in Women Undergoing IVF

Enteral L-Arginine Supplementation for Prevention of Necrotizing Enterocolitis in Very Low Birth Weight Neonates: A Double-Blind Randomized Pilot Study of Efficacy and Safety

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

GSTP1 and CYP2B6 Genetic Polymorphisms and the Risk of Bronchopulmonary Dysplasia in Preterm Neonates

Possible Implication of GSTP1 and NQO1 Polymorphisms on Natalizumab Response in Multiple Sclerosis

Inducible nitric oxide synthase expression and its prognostic significance in colorectal cancer

The G⁵¹⁶T CYP2B6 germline polymorphism affects the risk of acute myeloid leukemia and is associated with specific chromosomal abnormalities

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