Sophia Kitsiou: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Molecular analysis of patients with autistic behaviour

Andreas Pampanos, Konstantina Volaki, Loretta Thomaidou, Sotiris Giouroukos, Ourania Papadaki-Papandreou, Sophia Kitsiou-Tzeli, Emmanouel Kanavakis

Journal:

Annals of General Psychiatry

Year:

2008

Language:

english

File:

PDF, 82 KB

english, 2008

2

Mutation screening in the Greek population and evaluation of NLGN3 and NLGN4X genes causal factors for autism

Volaki, Konstantina, Pampanos, Andreas, Kitsiou-Tzeli, Sophia, Vrettou, Christina, Oikonomakis, Vasilis, Sofocleous, Christalena, Kanavakis, Emmanuel

Journal:

Psychiatric Genetics

Year:

2013

Language:

english

File:

PDF, 332 KB

english, 2013

3

Author reply

Eleni Leze, Loretta Thomaidis, Sophia Kitsiou-Tzeli…

Journal:

World Journal of Pediatrics

Year:

2013

Language:

english

File:

PDF, 151 KB

english, 2013

4

Tall Stature, Insulin Resistance, and Disturbed Behavior in a Girl with the Triple X Syndrome Harboring Three SHOX Genes: Offspring of a Father with Mosaic Klinefelter Syndrome but with Two Maternal X Chromosomes

Kanaka-Gantenbein, Christina, Kitsiou, Sophia, Mavrou, Ariadni, Stamoyannou, Lela, Kolialexi, Aggeliki, Kekou, Kyriaki, Liakopoulou, Magda, Chrousos, George

Journal:

Hormone Research

Year:

2004

Language:

english

File:

PDF, 121 KB

english, 2004

5

Three Novel Mutations in Greek Sotos Patients with Rare Clinical Manifestations

Leventopoulos, George, Kitsiou-Tzeli, Sophia, Psoni, Stavroula, Mavrou, Ariadni, Kanavakis, Emmanuel, Willems, Patrick, Fryssira, Helen

Journal:

Hormone Research

Year:

2009

Language:

english

File:

PDF, 166 KB

english, 2009

6

Identification of high frequency of Y chromosome deletions in patients with sex chromosome mosaicism and correlation with the clinical phenotype and Y-chromosome instability

Philippos C Patsalis, Nicos Skordis, Carolina Sismani, Ludmila Kousoulidou, George Koumbaris, Christina Eftychi, George Stavrides, Antonis Ioulianos, Sophia Kitsiou-Tzeli, Angeliki Galla-Voumvouraki,

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 85 KB

english, 2005

7

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

8

A Clinical Study of Sotos Syndrome Patients With Review of the Literature

George Leventopoulos, Sophia Kitsiou-Tzeli, Konstantinos Kritikos, Stavroula Psoni, Ariadni Mavrou, Emmanuel Kanavakis, Helen Fryssira

Journal:

Pediatric Neurology

Year:

2009

Language:

english

File:

PDF, 252 KB

english, 2009

9

Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the down syndrome

Sophia Kitsiou-Tzeli, Dr. Joseph J. Hallett, Leonard Atkins, Samuel A. Latt, Lewis B. Holmes, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1984

Language:

english

File:

PDF, 293 KB

english, 1984

10

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

Nikolaos Vogiatzakis, Kyriaki Kekou, Christalena Sophocleous, Sophia Kitsiou, Ariadni Mavrou, Chrisa Bakoula, Emmanouel Kanavakis

Journal:

Molecular Biotechnology

Year:

2007

Language:

english

File:

PDF, 370 KB

english, 2007

11

Clinical Manifestations and Molecular Investigation of 50 Patients with Williams Syndrome in the Greek Population

Amenta, Stella, Sofocleous, Christalena, Kolialexi, Angeliki, Thomaidis, Loretta, Giouroukos, Sotiris, Karavitakis, Emmanuel, Mavrou, Ariadni, Kitsiou, Sophia, Kanavakis, Emmanuel, Fryssira, Helen

Journal:

Pediatric Research

Year:

2005

File:

PDF, 1.00 MB

2005

12

Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome andPTPN11mutation analysis: the value of initial clinical assessment

Anna Papadopoulou, Michalis Issakidis, Evangelia Gole, Konstantina Kosma, Helen Fryssira, Andreas Fretzayas, Polyxeni Nicolaidou, Sophia Kitsiou-Tzeli

Journal:

European Journal of Pediatrics

Year:

2012

Language:

english

File:

PDF, 142 KB

english, 2012

13

TOBRAMYCIN DOSAGE IN INFANTS AND CHILDREN

Kafetzis, DimitrisA., Sinaniotis, ConstantinosA., Kitsiou-Tzeli, Sophia, Papadatos, ConstantinosJ.

Journal:

Year:

1978

Language:

english

File:

PDF, 143 KB

english, 1978

14

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

15

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

16

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

17

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

18

Calcium and Vitamin D Metabolism in Hypocalcemic Vitamin D-Resistant Rickets Carriers

Nicolaidou, Polyxeni, Papadopoulou, Anna, Georgouli, Helen, Matsinos, Y.G., Tsapra, Helen, Fretzayas, Andreas, Giannoulia-Karantana, Aglaia, Kitsiou, Sophia, Douros, Konstantinos, Papassotiriou, Ioann

Journal:

Hormone Research

Year:

2006

Language:

english

File:

PDF, 95 KB

english, 2006

19

Greece: The Hellenic Association of Medical Geneticists

Tsenghi, Christine, Tzeli-Kitsiou, Sophia

Journal:

Genetics in Medicine

Year:

2001

Language:

english

File:

PDF, 36 KB

english, 2001

20

Tumor development in three patients with Noonan syndrome

Helen Fryssira, George Leventopoulos, Stavroula Psoni, Sophia Kitsiou-Tzeli, Nikolaos Stavrianeas, Emmanuel Kanavakis

Journal:

European Journal of Pediatrics

Year:

2008

Language:

english

File:

PDF, 391 KB

english, 2008

21

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

22

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

23

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

24

Does the Rare A172G Mutation of PTPN11 Gene Convey a Mild Noonan Syndrome Phenotype?

Kitsiou-Tzeli, Sophia, Papadopoulou, Anna, Kanaka-Gantenbein, Christina, Fretzayas, Andreas, Daskalopoulos, Dimitris, Kanavakis, Emmanuel, Polyxeni, Nicolaidou

Journal:

Hormone Research

Year:

2006

Language:

english

File:

PDF, 128 KB

english, 2006

25

Severe proteus syndrome in an 18-month-old boy

Dr. Ariadne Malamitsi-Puchner, Sophia Kitsiou, Christos S. Bartsocas, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 1.05 MB

english, 1987

26

MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders

Stavroula Psoni, Christalena Sofocleous, Joanne Traeger-Synodinos, Sophia Kitsiou-Tzeli, Emmanuel Kanavakis, Helen Fryssira-Kanioura

Journal:

Brain and Development

Year:

2012

Language:

english

File:

PDF, 137 KB

english, 2012

27

A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder

Stavroula Psoni, Patrick J. Willems, Emmanuel Kanavakis, Ariadne Mavrou, Helen Frissyra, Joanne Traeger-Synodinos, Christalena Sofokleous, Periklis Makrythanassis, Sophia Kitsiou-Tzeli

Journal:

European Journal of Paediatric Neurology

Year:

2010

Language:

english

File:

PDF, 135 KB

english, 2010

28

Unusual Pathologic Findings in A Girl with Wolf-Hirschhorn Syndrome, Del (4p)

Kitsiou, Sophia, Bartsocas, C. S., Alexiou, D., Mourtzinis, D.

Journal:

Fetal and Pediatric Pathology

Year:

1986

Language:

english

File:

PDF, 292 KB

english, 1986

29

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

30

Detection and incidence of cryptic Y chromosome sequences in Turner syndrome patients

Philippos C Patsalis, Carolina Sismani, Michael I Hadjimarcou, Sophia Kitsiou-Tzeli, Aspasia Tzezou, Charalambos G Hadjiathanasiou, Voula Velissariou, Evangelia Lymberatou, Nicholas K Moschonas, Nicos

Journal:

Clinical Genetics

Year:

1998

Language:

english

File:

PDF, 4.52 MB

english, 1998

31

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

32

Clinical Manifestations and Molecular Investigation of 50 Patients with Williams Syndrome in the Greek Population

Amenta, Stella, Sofocleous, Christalena, Kolialexi, Angeliki, Thomaidis, Loretta, Giouroukos, Sotiris, Karavitakis, Emmanuel, Mavrou, Ariadni, Kitsiou, Sophia, Kanavakis, Emmanuel, Fryssira, Helen

Journal:

Pediatric Research

Year:

2005

Language:

english

File:

PDF, 1.00 MB

english, 2005

33

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

34

Okamoto syndrome in a girl of Caucasian origin

Margharita Markouri, Themistokles Karpathios, Argirios Dinopoulos, Achilleas Attilakos, Andrew Fretzayas, Chryssa Bakoula, Sophia Kitsiou-Tzeli

Journal:

Developmental Medicine & Child Neurology

Year:

2008

Language:

english

File:

PDF, 91 KB

english, 2008

35

Linkage Map on Chromosome 21q and the Association of a DNA Haplotype with a Propensity to Nondisjunction and Trisomy 21

STYLIANOS E. ANTONARAKIS, SMITA D. KITTUR, CATERINA METAXOTOU, CHRISTOS BARTSOCAS, SOPHIA KITSIOU, PAUL C. WATKINS, ACHYUT S. PATEL, ANDREW C. WARREN, JAMES F. GUSELLA, YORAM GRONER, ARAVINDA CHAKRAVA

Journal:

Annals of the New York Academy of Sciences

Year:

1985

Language:

english

File:

PDF, 611 KB

english, 1985

36

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

37

SURVEYOR on the Spot

Vogiatzakis, Nikolaos, Kekou, Kyriaki, Sophocleous, Christalena, Kitsiou, Sophia, Mavrou, Ariadni, Bakoula, Chrisa, Kanavakis, Emmanouel, Deltas, Constantinos, Voskarides, Konstantinos

Journal:

The Journal of Molecular Diagnostics

Year:

2010

Language:

english

File:

PDF, 46 KB

english, 2010

38

The c.504T>C (p.Asn168Asn) polymorphism in the ABCB4 gene as a predisposing factor for intrahepatic cholestasis of pregnancy in Greece

Sophia Kitsiou-Tzeli, Joanne Traeger-Synodinos, Eirini Giannatou, Petros Kaminopetros, Eleftheria Roma, Perikles Makrythanasis, Aspasia Tsezou

Journal:

Liver International

Year:

2010

Language:

english

File:

PDF, 73 KB

english, 2010

39

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

Loretta Thomaidis, Sophia Kitsiou-Tzeli, Elena Critselis, Hera Drandakis, Vassiliki Touliatou, Stelios Mantoudis, Eleni Leze, Aspasia Destouni, Joanne Traeger-Synodinos, Dimitrios Kafetzis, Emmanouel

Journal:

World Journal of Pediatrics

Year:

2012

Language:

english

File:

PDF, 204 KB

english, 2012

40

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

41

Phenotypic and Genotypic Variability in Four Males With MECP2 Gene Sequence Aberrations Including a Novel Deletion

Psoni, Stavroula, Sofocleous, Christalena, Traeger-Synodinos, Joanne, Kitsiou-Tzeli, Sophia, Kanavakis, Emmanuel, Fryssira-Kanioura, Helen

Journal:

Pediatric Research

Year:

2010

Language:

english

File:

PDF, 344 KB

english, 2010

42

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

43

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

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски