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1

Maternal epigenetics and fetal and neonatal growth

Kitsiou-Tzeli, Sofia, Tzetis, Maria

Journal:

Current Opinion in Endocrinology Diabetes and Obesity

Year:

2016

Language:

english

File:

PDF, 181 KB

english, 2016

2

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

Sofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, Katerina Anagnostopoulou, Maria Kontodiou, Nadezda Kosyakova, Elisabeth Ewers, Anja Weise, Antonios Garas, Sandro Orru, Thomas Liehr, Aikater

Journal:

Molecular Cytogenetics

Year:

2009

Language:

english

File:

PDF, 65 KB

english, 2009

3

Compound heterozygosity of a paternal submicroscopic deletion and a maternal missense mutation in POR gene: Antley-bixler syndrome phenotype in three sibling fetuses

Tzetis, Maria, Konstantinidou, Anastasia, Sofocleous, Christalena, Kosma, Konstantina, Mitrakos, Anastasios, Tzannatos, Christina, Kitsiou-Tzeli, Sofia

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2016

Language:

english

File:

PDF, 248 KB

english, 2016

4

Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA

Tsipi, Maria, Poulou, Myrto, Fylaktou, Eirini, Kosma, Konstantina, Tsoutsou, Eirini, Pons, Maria-Roser, Kokkinou, Eleftheria, Kitsiou-Tzeli, Sofia, Fryssira, Helen, Tzetis, Maria

Journal:

Journal of the Neurological Sciences

Year:

2018

Language:

english

File:

PDF, 711 KB

english, 2018

5

Enhancing university students' privacy literacy through an educational intervention: a Greek case-study

Sideri, Maria, Kitsiou, Angeliki, Tzortzaki, Eleni, Kalloniatis, Christos, Gritzalis, Stefanos

Journal:

International Journal of Electronic Governance

Year:

2019

File:

PDF, 342 KB

2019

6

Molecular cytogenetic characterization and origin of two de novo duplication 9p cases

Tsezou, Aspasia, Kitsiou, Sofia, Galla, Angeliki, Petersen, Michael B., Karadima, Georgia, Syrrou, Maria, Sahl�n, Sigrid, Blennow, Elisabeth

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 2.01 MB

english, 2000

7

FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population

Maria Syrrou, Ioannis Georgiou, Maria Grigoriadou, Michael B. Petersen, Sofia Kitsiou, Gerassimos Pagoulatos, Philippos C. Patsalis

Journal:

Genetic Epidemiology

Year:

1998

Language:

english

File:

PDF, 25 KB

english, 1998

8

De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature

Sophia Kitsiou-Tzeli, Maria Tzetis, Christalena Sofocleous, Christina Vrettou, Athena Xaidara, Krinio Giannikou, Andreas Pampanos, Ariadne Mavrou, E. Kanavakis

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 123 KB

english, 2010

9

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

Sofia Kitsiou-Tzeli, Emmanouil Manolakos, Magdalini Lagou, Maria Kontodiou, Nadezda Kosyakova, Elisabeth Ewers, Anja Weise, Antonios Garas, Sandro Orru, Thomas Liehr, Aikaterini Metaxotou

Journal:

Molecular Cytogenetics

Year:

2009

Language:

english

File:

PDF, 641 KB

english, 2009

10

Long-term follow-up of a multifocal hepatic mesenchymal hamartoma producing a-fetoprotein

Andrew Fretzayas, Maria Moustaki, Sofia Kitsiou, Georgia Nychtari, E. Alexopoulou

Journal:

Pediatric Surgery International

Year:

2009

Language:

english

File:

PDF, 194 KB

english, 2009

11

Gilbert syndrome: analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population

Emmanuel Kavazarakis, Aspasia Tsezou, Maria Tzetis, Androniki Hadjidimoula, Sofia Kitsiou, Emmanuel Kanavakis, Themistocles Karpathios

Journal:

European Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 66 KB

english, 2000

12

The clinical pattern of group C streptococcal pharyngitis in children

Andrew Fretzayas, Maria Moustaki, Sofia Kitsiou, Georgia Nychtari, Polyxeni Nicolaidou

Journal:

Journal of Infection and Chemotherapy

Year:

2009

Language:

english

File:

PDF, 210 KB

english, 2009

13

Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene

Sofia KITSIOU-TZELI, Patrick WILLEMS, Maria KOSMADAKI, Eleni LEZE, Christine VRETTOU, Emmanuel KANAVAKIS, Alexandra KATSAROU

Journal:

The Journal of Dermatology

Year:

2011

Language:

english

File:

PDF, 290 KB

english, 2011

14

Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome

Philippos C. Patsalis, Michael I. Hadjimarcou, Voula Velissariou, Sophia Kitsiou-Tzeli, Christina Zera, Maria Syrrou, Evangelia Lyberatou, Aspasia Tsezou, Angeliki Galla, Nicos Skordis

Journal:

Clinical Genetics

Year:

1997

Language:

english

File:

PDF, 832 KB

english, 1997

15

Familial Pelizaeus–Merzbacher disease caused by a 320.6-kb Xq22.2 duplication and the pathological findings of a male fetus

Sophia Kitsiou-Tzeli, Anastasia Konstantinidou, Christalena Sofocleous, Konstantina Kosma, Areti Syrmou, Krinio Giannikou, Stavros Sifakis, Periklis Makrythanasis, Maria Tzetis

Journal:

Birth Defects Research Part A: Clinical and Molecular Teratology

Year:

2012

Language:

english

File:

PDF, 1.03 MB

english, 2012

16

Successful Pain Relief of Cutaneous Leiomyomata Due to Reed Syndrome with the Combination Treatment of Pregabalin and Duloxetine

Georgia Kostopanagiotou, Chrysa Arvaniti, Maria Chrysanthi Kitsiou, Stella Apostolaki, Katerina Chatzimichael, Paraskevi Matsota

Journal:

Journal of Pain and Symptom Management

Year:

2009

Language:

english

File:

PDF, 52 KB

english, 2009

17

The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization

Tzetis, Maria, Kitsiou-Tzeli, Sofia, Frysira, Helen, Xaidara, Athena, Kanavakis, Emmanuel

Journal:

Expert Review of Molecular Diagnostics

Year:

2012

Language:

english

File:

PDF, 369 KB

english, 2012

18

Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1

Bernard Thienpont, Eftychia Dimitriadou, Katerina Theodoropoulos, Jeroen Breckpot, Helen Fryssira, Sophia Kitsiou-Tzeli, Meropi Tzoufi, Joris R. Vermeesch, Maria Syrrou, Koen Devriendt

Journal:

European Journal of Medical Genetics

Year:

2009

Language:

english

File:

PDF, 166 KB

english, 2009

19

Microdeletion and microduplication 17q21.31 plus an additional CNV, in patients with intellectual disability, identified by array-CGH

Sophia Kitsiou-Tzeli, Helen Frysira, Krinio Giannikou, Areti Syrmou, Konstantina Kosma, Georgia Kakourou, Eleni Leze, Christalena Sofocleous, Emmanuel Kanavakis, Maria Tzetis

Journal:

Year:

2012

Language:

english

File:

PDF, 624 KB

english, 2012

20

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

Krinio Giannikou, Helen Fryssira, Vasilis Oikonomakis, Areti Syrmou, Konstantina Kosma, Maria Tzetis, Sofia Kitsiou-Tzeli, Emmanouel Kanavakis

Journal:

Year:

2012

Language:

english

File:

PDF, 697 KB

english, 2012

21

The circadian profile of extrasystolic arrhythmia: its relationship to heart rate and blood pressure

Dimitris A. Sideris, Savvas T. Toumanidis, Maria Anastasiou-Nana, Nikos Zakopoulos, Anastasia Kitsiou, Kostas Tsagarakis, Spyridon D. Moulopoulos

Journal:

International Journal of Cardiology

Year:

1992

Language:

english

File:

PDF, 901 KB

english, 1992

22

Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease

Syrmou, Areti, Tzetis, Maria, Fryssira, Helen, Kosma, Konstantina, Oikonomakis, Vasilis, Giannikou, Krinio, Makrythanasis, Periklis, Kitsiou-Tzeli, Sophia, Kanavakis, Emmanuel

Journal:

Pediatric Research

Year:

2013

Language:

english

File:

PDF, 609 KB

english, 2013

23

Novel and known nephrin gene (NPHS1) mutations in two Greek cases with congenital nephrotic syndrome including a complex genotype

FYLAKTOU, IRENE, MEGREMIS, SPYRIDON, MITSIONI, ANDROMACHI, KITSIOU-TZELI, SOFIA, KOSMA, KONSTANTINA, BITSORI, MARIA, STEFANIDIS, CONSTANTINOS J., KANAVAKIS, EMMANUEL, SYNODINOS, JOANNE TRAEGER

Journal:

Journal of Genetics

Year:

2013

Language:

english

File:

PDF, 755 KB

english, 2013

24

Are ALOX5AP gene SNPs a risk or protective factor for stroke?

Papapostolou, Apostolis, Spengos, Kostas, Fylaktou, Irene, Poulou, Myrto, Gountas, Ilias, Kitsiou-Tzeli, Sophia, Kanavakis, Emmanuel, Tzetis, Maria

Journal:

Year:

2014

Language:

english

File:

PDF, 226 KB

english, 2014

25

A Substitution Involving the NLGN4 Gene Associated with Autistic Behavior in the Greek Population

Pampanos, Andreas, Volaki, Konstantina, Kanavakis, Emmanuel, Papandreou, Ourania, Youroukos, Sotiris, Thomaidis, Loretta, Karkelis, Savvas, Tzetis, Maria, Kitsiou-Tzeli, Sophia

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2009

Language:

english

File:

PDF, 20.85 MB

english, 2009

26

Genetic Polymorphisms in the UGT1A1 Gene and Breast Cancer Risk in Greek Women

Tsezou, Aspasia, Tzetis, Maria, Giannatou, Eirini, Gennatas, Constantinos, Pampanos, Andreas, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia

Journal:

Genetic Testing

Year:

2007

Language:

english

File:

PDF, 67 KB

english, 2007

27

Microduplication 3q13.2q13.31 identified in a male with dysmorphic features and multiple congenital anomalies

Karavitakis, Emmanouil, Kitsiou-Tzeli, Sofia, Xaidara, Athena, Kosma, Konstantina, Makrythanasis, Periklis, Apazidou, Eleni, Kanavakis, Emmanuel, Tzetis, Maria

Journal:

American Journal of Medical Genetics Part A

Year:

2014

Language:

english

File:

PDF, 270 KB

english, 2014

28

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

Makrythanasis, Periklis, Tzetis, Maria, Rapti, Aggeliki, Papatheodorou, Athanasios, Tsipi, Maria, Kitsiou, Sophia, Tsiamouri, Alexia, Poulou, Myrto, Roussos, Charis, Kanavakis, Emmanouel

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2010

Language:

english

File:

PDF, 104 KB

english, 2010

29

Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population

Tsezou, Aspasia, Tzetis, Maria, Giannatou, Eirini, Spanos, Ierotheos, Roma, Eleutheria, Fretzayas, Alexandros, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2009

Language:

english

File:

PDF, 72 KB

english, 2009

30

Breast Metastasis from Uterine Leiomyosarcoma Diagnosed by Fine Needle Aspiration

Pappa, Lina, Zagorianakou, Nektaria, Kitsiou, Evangelia, Sintou-Mantela, Evdoxia, Bafa, Maria, Malamou-Mitsi, Vassiliki

Journal:

Acta Cytologica

Year:

2008

Language:

english

File:

PDF, 524 KB

english, 2008

31

Complex preimplantation genetic diagnosis for beta-thalassaemia, sideroblastic anaemia, and human leukocyte antigen (HLA)-typing

Kakourou, Georgia, Vrettou, Christina, Kattamis, Antonis, Destouni, Aspasia, Poulou, Myrto, Moutafi, Maria, Kokkali, Georgia, Pantos, Konstantinos, Davies, Stephen, Kitsiou-Tzeli, Sophia, Kanavakis, E

Journal:

Systems Biology in Reproductive Medicine

Year:

2015

Language:

english

File:

PDF, 489 KB

english, 2015

32

Genomic screening of ABCA4 and array CGH analysis underline the genetic variability of Greek patients with inherited retinal diseases

Tsipi, Maria, Tzetis, Maria, Kosma, Konstantina, Moschos, Marilita, Braoudaki, Maria, Poulou, Myrto, Kanavakis, Emmanuel, Kitsiou-Tzeli, Sofia

Journal:

Year:

2016

Language:

english

File:

PDF, 280 KB

english, 2016

33

An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4

Selenti, Nikoletta, Tzetis, Maria, Braoudaki, Maria, Giannikou, Krinio, Kitsiou-Tzeli, Sofia, Fryssira, Helen

Journal:

Molecular Cytogenetics

Year:

2015

Language:

english

File:

PDF, 916 KB

english, 2015

34

Erratum to: An interstitial deletion at 8q23.1-q24.12 associated with Langer-Giedion syndrome/ Trichorhinophalangeal syndrome (TRPS) type II and Cornelia de Lange syndrome 4

Selenti, Nikoletta, Tzetis, Maria, Braoudaki, Maria, Giannikou, Krinio, Kitsiou-Tzeli, Sofia, Fryssira, Helen

Journal:

Molecular Cytogenetics

Year:

2015

Language:

english

File:

PDF, 294 KB

english, 2015

35

Issues and perceptions for ISO 9000 implementation in Greek academic libraries

Kostagiolas, Petros A., Kitsiou, Maria B.

Journal:

Library Management

Year:

2008

Language:

english

File:

PDF, 273 KB

english, 2008

36

Rhabdomyosarcoma in a Patient With Noonan Syndrome Phenotype and Review of the Literature

Moschovi, Maria, Vassiliki, Touliatou, Anna, Papadopoulou, Maria-Alexandra, Mayakou, Polyxeni, Nikolaidou-Karpathiou, Sophia, Kitsiou-Tzeli

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2007

Language:

english

File:

PDF, 161 KB

english, 2007

37

Caveolinopathies in Greece

Papadopoulos, Constantinos, Papadimas, George K., Kekou, Kyriaki, Spengos, Konstantinos, Svigou, Maria, Kitsiou-Tzeli, Sofia, Manta, Panagiota

Journal:

The Neurologist

Year:

2015

Language:

english

File:

PDF, 211 KB

english, 2015

38

A dynamic trinucleotide repeat (TNR) expansion in the DMD GENE

Kekou, Kyriaki, Sofocleous, Christalena, Papadimas, George, Petihakis, Dimitris, Svingou, Maria, Pons, Roser-Maria, Vorgia, Pelagia, Gika, Artemis, Kitsiou, Sophia, Kanavakis, Emmanuel

Journal:

Molecular and Cellular Probes

Year:

2016

Language:

english

File:

PDF, 2.02 MB

english, 2016

39

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Syndrome: Additional Clinical Features

Makrygianni, Evanthia A., Papadimas, George K., Vartzelis, George, Georgala, Maria, Tzetis, Maria, Poulou, Myrto, Kitsiou-Tzeli, Sophia, Pons, Roser

Journal:

Pediatric Neurology

Year:

2017

Language:

english

File:

PDF, 139 KB

english, 2017

40

[ACM Press the 20th Pan-Hellenic Conference - Patras, Greece (2016.11.10-2016.11.12)] Proceedings of the 20th Pan-Hellenic Conference on Informatics - PCI '16 - Self-disclosure, Privacy concerns and Social Capital benefits interaction in FB

Tzortzaki, Eleni, Kitsiou, Angeliki, Sideri, Maria, Gritzalis, Stefanos

Year:

2016

Language:

english

File:

PDF, 397 KB

english, 2016

41

Application of high resolution array comparative genomic hybridization in children with unknown syndromic microcephaly

Tsoutsou, Eirini, Tzetis, Maria, Giannikou, Krinio, Braoudaki, Maria, Mitrakos, Anastasis, Amenta, Stella, Selenti, Nikoletta, Kanavakis, Emmanouil, Zafeiriou, Dimitrios, Kitsiou-Tzeli, Sophia, Fryssi

Journal:

Pediatric Research

Year:

2017

Language:

english

File:

PDF, 1.10 MB

english, 2017

42

A Female Patient with Xq28 Microduplication Presenting with Myotubular Myopathy, Confirmed with a Custom-Designed X-array

Kosma, Konstantina, Mitrakos, Anastasios, Sofokleous, Christalena, Papadimas, George, Fryssira, Helena, Kitsiou-Tzeli, Sofia, Tzetis, Maria

Journal:

Neuropediatrics

Year:

2018

Language:

english

File:

PDF, 66 KB

english, 2018

43

High resolution Chromosomal Microarray Analysis (CMA) enhances the genetic profile of pediatric B-cell Acute Lymphoblastic Leukemia patients

Mitrakos, Anastasios, Kattamis, Antonis, Katsibardi, Katerina, Papadhimitriou, Stefanos, Kitsiou-Tzeli, Sophia, Kanavakis, Emmanuel, Tzetis, Maria

Journal:

Leukemia Research

Year:

2019

Language:

english

File:

PDF, 880 KB

english, 2019

44

Sharing secrets, revealing thoughts and feelings: perceptions about disclosure practices and anonymity in a FB university students' community

Sideri, Maria, Kitsiou, Angeliki, Kalloniatis, Christos, Gritzalis, Stefanos

Journal:

International Journal of Electronic Governance

Year:

2017

File:

PDF, 443 KB

2017