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Sophia Kitsiou-Tzeli

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Greece

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Glucuronosyltransferase

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Areti Syrmou; Maria Tzetis; Helen Fryssira; Krinio Giannikou; Sophia Kitsiou-Tzeli; Konstantina Kosma; Periklis Makrythanasis; Vasilis Oikonomakis; Emmanuel Kanavakis
Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.
Eleni Leze; Loretta Thomaidis; Sophia Kitsiou-Tzeli; Emmanouel Kanavakis
Author reply.
Loretta Thomaidis; Vassiliki Touliatou; Joanne Traeger-Synodinos; Sophia Kitsiou-Tzeli; Eleni Leze; Stelios Mantoudis; Elena Critselis; Aspasia Destouni; Hera Drandakis; Dimitrios Kafetzis; Emmanouel Kanavakis
Psychomotor development of children born after preimplantation genetic diagnosis and parental stress evaluation.

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All Publications

2013: Areti Syrmou; Maria Tzetis; Helen Fryssira; Krinio Giannikou; Sophia Kitsiou-Tzeli; Konstantina Kosma; Periklis Makrythanasis; Vasilis Oikonomakis; Emmanuel Kanavakis
Array comparative genomic hybridization as a clinical diagnostic tool in syndromic and nonsyndromic congenital heart disease.
Pediatric research 2013;73(6):772-6.
2013: Eleni Leze; Loretta Thomaidis; Sophia Kitsiou-Tzeli; Emmanouel Kanavakis
Author reply.
World journal of pediatrics : WJP 2013;9(1):90-1.
2012: Loretta Thomaidis; Vassiliki Touliatou; Joanne Traeger-Synodinos; Sophia Kitsiou-Tzeli; Eleni Leze; Stelios Mantoudis; Elena Critselis; Aspasia Destouni; Hera Drandakis; Dimitrios Kafetzis; Emmanouel Kanavakis
Psychomotor development of children born after preimplantation genetic diagnosis and parental stress evaluation.
World journal of pediatrics : WJP 2012;8(4):309-16.
2012: Krinio Giannikou; Helen Fryssira; Sophia Kitsiou-Tzeli; Konstantina Kosma; Vasilis Oikonomakis; Areti Syrmou; Maria Tzetis; Emmanouel Kanavakis
Further delineation of novel 1p36 rearrangements by array-CGH analysis: narrowing the breakpoints and clarifying the "extended" phenotype.
Gene 2012;506(2):360-8.
2012: Sophia Kitsiou-Tzeli; Sophia Malaktari-Skarantavou; Spyridon Megremis; Christodoulos Stefanadis; Joanne Traeger-Synodinos; Charalampos Vlachopoulos; Maria Deligiorgi; Irene Fylaktou; Christina Kanaka-Gantenbein; Emmanuel Kanavakis
Sertoli cell tumor and gonadoblastoma in an untreated 29-year-old 46,XY phenotypic male with Frasier syndrome carrying a WT1 IVS9+4C>T mutation.
Hormones (Athens, Greece) 2012;11(3):361-7.
2012: Maria Tzetis; Michael Choulakis; Krinio Giannikou; Aggeliki Kolialexi; Konstantina Kosma; Eleni Leze; Periklis Makrythanasis; Vasilis Oikonomakis; Christalena Sofocleous; Kalliopi Stefanaki; Areti Syrmou; Sophia Kitsiou-Tzeli
An unusual case of Cat-Eye syndrome phenotype and extragonadal mature teratoma: review of the literature.
Birth defects research. Part A, Clinical and molecular teratology 2012;94(7):561-6.
2012: Maria Tzetis; Athena Xaidara; Helen Frysira; Sophia Kitsiou-Tzeli; Emmanuel Kanavakis
The clinical utility of molecular karyotyping using high-resolution array-comparative genomic hybridization.
Expert review of molecular diagnostics 2012;12(5):449-57.
2012: Sophia Kitsiou-Tzeli; Anastasia E Konstantinidou; Konstantina Kosma; Periklis Makrythanasis; Stavros Sifakis; Christalena Sofocleous; Areti Syrmou; Krinio Giannikou; Maria Tzetis
Familial Pelizaeus-Merzbacher disease caused by a 320.6-kb Xq22.2 duplication and the pathological findings of a male fetus.
Birth defects research. Part A, Clinical and molecular teratology 2012;94(6):494-8.
2012: Stavroula Psoni; Christalena Sofocleous; Joanne Traeger-Synodinos; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli; Helen Fryssira-Kanioura
MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders.
Brain & development 2012;34(6):487-95.
2012: G Christopoulou; E Kanavakis; Sophia Kitsiou-Tzeli; Anastasia E Konstantinidou; Aspasia Tsezou; M Tzetis; Voula Velissariou
Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3-p14 and 4.22 Mb in 10q26.3.
European journal of medical genetics 2012;55(1):75-9.
2011: Sophia Kitsiou-Tzeli; Maria Kosmadaki; Eleni Leze; Christina Vrettou; Patrick Willems; Emmanuel Kanavakis; A Katsarou
Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene.
The Journal of dermatology 2011;38(12):1205-8.
2011: Vassilis Papanikolaou; Ioannis Dimou; Stephanie Dubos; Dimitrios Iliopoulos; Constantin Kappas; Sophia Kitsiou-Tzeli; Aspasia Tsezou
Survivin regulation by HER2 through NF-κB and c-myc in irradiated breast cancer cells.
Journal of cellular and molecular medicine 2011;15(7):1542-50.
2011: Vassilis Papanikolaou; Evangelos Athanassiou; Stephanie Dubos; Ioannis Dimou; Ioanna Papathanasiou; Sophia Kitsiou-Tzeli; Constantin Kappas; Aspasia Tsezou
hTERT regulation by NF-κB and c-myc in irradiated HER2-positive breast cancer cells.
International journal of radiation biology 2011;87(6):609-21.
2011: George Koumbaris; Hariklia Hatzisevastou-Loukidou; Angelos Alexandrou; Marios Ioannides; Christodoulos Christodoulou; Tomas Fitzgerald; Diana Rajan; Stephen Clayton; Sophia Kitsiou-Tzeli; Joris R Vermeesch; Nicos Skordis; Pavlos Antoniou; Ants Kurg; Ioannis Georgiou; Nigel P Carter; Philippos C Patsalis
FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation.
Human molecular genetics 2011;20(10):1925-36.
2011: Emmanouil Manolakos; Catherine Sarri; Annalisa Vetro; Konstantinos Kefalas; Eleni Leze; Christalena Sofocleus; George Kitsos; Konstantina Merou; Haris Kokotas; Anna Papadopoulou; Achilleas Attilakos; Michael B Petersen; Sophia Kitsiou-Tzeli
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy.
Molecular cytogenetics 2011;4(1):11.
2011: Emmanouil Manolakos; Catherine Sarri; Annalisa Vetro; Konstantinos Kefalas; Eleni Leze; Christalena Sofocleus; George Kitsos; Konstantina Merou; Haris Kokotas; Anna Papadopoulou; Achilleas Attilakos; Michael B Petersen; Sophia Kitsiou-Tzeli
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy.
Molecular cytogenetics 2011;4(1):6.
2010: Periklis Makrythanasis; Maria Tzetis; Aggeliki Rapti; Athanasios Papatheodorou; Maria Tsipi; Sophia Kitsiou-Tzeli; Alexia Tsiamouri; Myrto Poulou; Charis Roussos; Emmanuel Kanavakis
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;14(4):577-84.
2010: Sophia Kitsiou-Tzeli; Maria Tzetis; Christalena Sofocleous; Christina Vrettou; Athena Xaidara; Krinio Giannikou; Andreas Pampanos; Ariadni Mavrou; Emmanuel Kanavakis
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.
American journal of medical genetics. Part A 2010;152A(8):1925-32.
2010: Sophia Kitsiou-Tzeli; Christina Vrettou; Eleni Leze; Periklis Makrythanasis; Emmanouel Kanavakis; Patrick Willems
Milroy's primary congenital lymphedema in a male infant and review of the literature.
In vivo (Athens, Greece) 2010;24(3):309-14.
2010: Stavroula Psoni; Christalena Sofocleous; Joanne Traeger-Synodinos; Sophia Kitsiou-Tzeli; Emmanuel Kanavakis; Helen Fryssira-Kanioura
Phenotypic and genotypic variability in four males with MECP2 gene sequence aberrations including a novel deletion.
Pediatric research 2010;67(5):551-6.
2010: Nikolaos Vogiatzakis; Kyriaki Kekou; Christalena Sophocleous; Sophia Kitsiou-Tzeli; Ariadni Mavrou; Chrisa Bakoula; Emmanouel Kanavakis
SURVEYOR on the spot: strengths and weaknesses in molecular diagnostics.
The Journal of molecular diagnostics : JMD 2010;12(2):265; author reply 265-6.
2010: Sophia Kitsiou-Tzeli; Joanne Traeger-Synodinos; Eirini Giannatou; Petros Kaminopetros; Eleftheria Roma; Perikles Makrythanasis; Aspasia Tsezou
The c.504T>C (p.Asn168Asn) polymorphism in the ABCB4 gene as a predisposing factor for intrahepatic cholestasis of pregnancy in Greece.
Liver international : official journal of the International Association for the Study of the Liver 2010;30(3):489-91.
2010: Stavroula Psoni; Patrick J Willems; Emmanuel Kanavakis; Ariadne Mavrou; Helen Frissyra; Joanne Traeger-Synodinos; Christalena Sofokleous; Periklis Makrythanassis; Sophia Kitsiou-Tzeli
A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2010;14(2):188-91.
2010: Argirios Dinopoulos; Anna Papadopoulou; Panagiota Manta; Kyriaki Kekou; Tassos Kanelopoulos; Andreas Fretzayas; Sophia Kitsiou-Tzeli
Coinheritance of Noonan syndrome and Becker muscular dystrophy.
Neuromuscular disorders : NMD 2010;20(1):61-3.
2009: Vassilis Papanikolaou; Dimitrios Iliopoulos; Ioannis Dimou; Stephanie Dubos; Ioannis Tsougos; Kyriaki Theodorou; Sophia Kitsiou-Tzeli; Aspasia Tsezou
The involvement of HER2 and p53 status in the regulation of telomerase in irradiated breast cancer cells.
International journal of oncology 2009;35(5):1141-9.
2009: Bernard Thienpont; Eftychia Dimitriadou; Katerina Theodoropoulos; Jeroen Breckpot; Helen Fryssira; Sophia Kitsiou-Tzeli; Meropi Tzoufi; Joris R Vermeesch; Maria Syrrou; koenraad devriendt
Refining the locus of branchio-otic syndrome 2 (BOS2) to a 5.25 Mb locus on chromosome 1q31.3q32.1.
European journal of medical genetics 2009;52(6):393-7.
2009: Lorena Travaglini; Francesco Brancati; Tania Attie-Bitach; Sophie Audollent; Enrico Bertini; Josseline Kaplan; Isabelle Perrault; Miriam Iannicelli; Brunella Mancuso; Luciana Rigoli; Jean-Michel Rozet; Dominika Swistun; Jerlyn Tolentino; Bruno Dallapiccola; Joseph G Gleeson; Enza Maria Valente; A Zankl; R Leventer; P Grattan-Smith; A Janecke; M D'Hooghe; Y Sznajer; R Van Coster; L Demerleir; K Dias; C Moco; A Moreira; C Ae Kim; Gustavo Maegawa; D Petkovic; G M H Abdel-Salam; A Abdel-Aleem; M S Zaki; I Marti; S Quijano-Roy; S Sigaudy; P de Lonlay; S Romano; R Touraine; M Koenig; C Lagier-Tourenne; J Messer; P Collignon; N Wolf; H Philippi; Sophia Kitsiou-Tzeli; S Halldorsson; J Johannsdottir; P Ludvigsson; S R Phadke; V Udani; B Stuart; A Magee; D Lev; M Michelson; B Ben-Zeev; R Fischetto; F Benedicenti; F Stanzial; R Borgatti; P Accorsi; S Battaglia; E Fazzi; L Giordano; L Pinelli; L Boccone; S Bigoni; A Ferlini; M A Donati; G Caridi; M T Divizia; F Faravelli; G Ghiggeri; A Pessagno; M Briguglio; S Briuglia; C D Salpietro; G Tortorella; A Adami; P Castorina; F Lalatta; G Marra; D Riva; Barbara Scelsa; L Spaccini; Graziella Uziel; E Del Giudice; A M Laverda; K Ludwig; A Permunian; A Suppiej; S Signorini; C Uggetti; R Battini; M Di Giacomo; M R Cilio; M L Di Sabato; V Leuzzi; P Parisi; M Pollazzon; M Silengo; R De Vescovi; D Greco; Corrado Romano; M Cazzagon; A Simonati; A A Al-Tawari; L Bastaki; A Mégarbané; V Sabolic Avramovska; M M de Jong; P Stromme; R Koul; A Rajab; M Azam; C Barbot; L Martorell Sampol; B Rodriguez; I Pascual-Castroviejo; S Teber; B Anlar; S Comu; E Karaca; H Kayserili; A Yüksel; M Akcakus; L Al Gazali; L Sztriha; D Nicholl; C G Woods; C Bennett; J Hurst; E Sheridan; A Barnicoat; Raoul Hennekam; M Lees; E Blair; S Bernes; H Sanchez; A E Clark; E DeMarco; C Donahue; Elliott H Sherr; J Hahn; T D Sanger; T E Gallager; W B Dobyns; C Daugherty; K S Krishnamoorthy; D Sarco; Christopher Walsh; T McKanna; J Milisa; W K Chung; D C De Vivo; Hillary Raynes; R Schubert; A Seward; D G Brooks; A Goldstein; J Caldwell; E Finsecke; B L Maria; K Holden; R P Cruse; K J Swoboda; D Viskochil
Expanding CEP290 mutational spectrum in ciliopathies.
American journal of medical genetics. Part A 2009;149A(10):2173-80.
2009: Andreas Pampanos; Konstantina Volaki; Emmanuel Kanavakis; Ourania Papandreou; Sotiris Youroukos; Loretta Thomaidis; Savvas Karkelis; Maria Tzetis; Sophia Kitsiou-Tzeli
A substitution involving the NLGN4 gene associated with autistic behavior in the Greek population.
Genetic testing and molecular biomarkers 2009;13(5):611-5.
2009: C Christofidou; C Sofocleous; Christina Vrettou; A Destouni; Joanne Traeger-Synodinos; Kyriaki Kekou; Giles Palmer; G Kokkali; Ariadni Mavrou; Sophia Kitsiou-Tzeli; Emmanuel Kanavakis
PGD for X-linked and gender-dependent disorders using a robust, flexible single-tube PCR protocol.
Reproductive biomedicine online 2009;19(3):418-25.
2009: Andreas Fretzayas; Maria Moustaki; Sophia Kitsiou-Tzeli; Georgia Nychtari; Polyxeni Nicolaidou
The clinical pattern of group C streptococcal pharyngitis in children.
Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 2009;15(4):228-32.
2009: Achilleas Attilakos; Alexia Prassouli; George Hadjigeorgiou; Evangelia Lagona; Sophia Kitsiou-Tzeli; Angeliki Galla; Anastasia Stasinopoulou; Themistocles Karpathios
Acute acalculous cholecystitis in children with Epstein-Barr virus infection: a role for Gilbert's syndrome?
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases 2009;13(4):e161-4.
2009: George Leventopoulos; Sophia Kitsiou-Tzeli; Konstantinos Kritikos; Stavroula Psoni; Ariadni Mavrou; Emmanuel Kanavakis; Helen Fryssira
A clinical study of Sotos syndrome patients with review of the literature.
Pediatric neurology 2009;40(5):357-64.
2009: Spyridon Megremis; Andromachi Mitsioni; Artemis G Mitsioni; Irene Fylaktou; Sophia Kitsiou-Tzeli; Constantinos Stefanidis; Emmanuel Kanavakis; Joanne Traeger-Synodinos
Nucleotide variations in the NPHS2 gene in Greek children with steroid-resistant nephrotic syndrome.
Genetic testing and molecular biomarkers 2009;13(2):249-56.
2009: Andreas Fretzayas; Maria Moustaki; Sophia Kitsiou-Tzeli; Georgia Nychtari; Efthymia Alexopoulou
Long-term follow-up of a multifocal hepatic mesenchymal hamartoma producing a-fetoprotein.
Pediatric surgery international 2009;25(4):381-4.
2009: Robert Lyle; Frédérique Béna; Sarantis Gagos; Corinne Gehrig; Gipsy Lopez; Albert Schinzel; James Lespinasse; Armand Bottani; Sophie Dahoun; Laurence Taine; Martine Doco-Fenzy; Pascale Cornillet-Lefèbvre; Anna Pelet; Stanislas Lyonnet; Annick Toutain; Laurence Colleaux; Jürgen Horst; Ingo Kennerknecht; Nobuaki Wakamatsu; Maria Descartes; Judy C Franklin; Lina Florentin-Arar; Sophia Kitsiou-Tzeli; Emilie Aït Yahya-Graison; Maher Costantine; Pierre-Marie Sinet; Jean M Delabar; Stylianos E Antonarakis
Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21.
European journal of human genetics : EJHG 2009;17(4):454-66.
2009: Aspasia Destouni; Christina Vrettou; Dionisis Antonatos; George Chouliaras; Joanne Traeger-Synodinos; Sotiris Patsilinakos; Sophia Kitsiou-Tzeli; Dimitrios Tsigas; Emmanouel Kanavakis
Cell-free DNA levels in acute myocardial infarction patients during hospitalization.
Acta cardiologica 2009;64(1):51-7.
2009: Aspasia Tsezou; Maria Tzetis; Eirini Giannatou; Ierotheos Spanos; Eleutheria Roma; Alexandros Fretzayas; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli
Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population.
Genetic testing and molecular biomarkers 2009;13(1):143-6.
2009: Eleanna Giannatou; H Leze; A Katana; Aggeliki Kolialexi; Ariadni Mavrou; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli
Unilateral microtia in an infant with trisomy 18 mosaicism.
Genetic counseling (Geneva, Switzerland) 2009;20(2):181-7.
2009: Sophia Kitsiou-Tzeli; Emmanouil Manolakos; Magdalini Lagou; Katerina Anagnostopoulou; Maria Kontodiou; Nadezda Kosyakova; Elisabeth Ewers; Anja Weise; Antonios Garas; Sandro Orru; Thomas Liehr; Aikaterini Metaxotou
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.
Molecular cytogenetics 2009;2():8.
2009: Sophia Kitsiou-Tzeli; Emmanouil Manolakos; Magdalini Lagou; Maria Kontodiou; Nadezda Kosyakova; Elisabeth Ewers; Anja Weise; Antonios Garas; Sandro Orru; Thomas Liehr; Aikaterini Metaxotou
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.
Molecular cytogenetics 2009;2():1.
2009: George Leventopoulos; Sophia Kitsiou-Tzeli; Stavroula Psoni; Ariadni Mavrou; Emmanuel Kanavakis; Patrick Willems; Helen Fryssira
Three novel mutations in greek sotos patients with rare clinical manifestations.
Hormone research 2009;71(1):45-51.
2008: Margharita Markouri; Themistokles Karpathios; Argirios Dinopoulos; Achilleas Attilakos; Andrew Fretzayas; Chryssa Bakoula; Sophia Kitsiou-Tzeli
Okamoto syndrome in a girl of Caucasian origin.
Developmental medicine and child neurology 2008;50(12):950-2.
2008: Aspasia Tsezou; Lazaros Poultsides; Fotini Kostopoulou; Elias Zintzaras; Maria Satra; Sophia Kitsiou-Tzeli; Konstantinos N Malizos
Influence of interleukin 1alpha (IL-1alpha), IL-4, and IL-6 polymorphisms on genetic susceptibility to chronic osteomyelitis.
Clinical and vaccine immunology : CVI 2008;15(12):1888-90.
2008: Angeliki Galani; Christalena Sofocleous; Feneli Karahaliou; Asteroula Papathanasiou; Sophia Kitsiou-Tzeli; Ariadni Kalpini-Mavrou
Sex-reversed phenotype in association with two novel mutations c.2494delA and c.T3004C in the ligand-binding domain of the androgen receptor gene.
Fertility and sterility 2008;90(5):2008.e1-4.
2008: Helen Fryssira; George Leventopoulos; Stavroula Psoni; Sophia Kitsiou-Tzeli; Nikolaos Stavrianeas; Emmanuel Kanavakis
Tumor development in three patients with Noonan syndrome.
European journal of pediatrics 2008;167(9):1025-31.
2008: Sophia Kitsiou-Tzeli; Carolina Sismani; Margarita Karkaletsi; Lina Florentin; Anastassios Anastassiou; George Koumbaris; Paola Evangelidou; Paola Enangelidou; Emmanouil Agapitos; Philippos C Patsalis; Voula Velissariou
Prenatal diagnosis of a de novo partial trisomy 10p12.1-12.2 pter originating from an unbalanced translocation onto 15qter and confirmed with array CGH.
Prenatal diagnosis 2008;28(8):770-2.
2008: C Sofocleous; Sophia Kitsiou-Tzeli; Helen Fryssira; Aggeliki Kolialexi; M Kalaitzidaki; Eleftheria Roma; George Th Tsangaris; C Chistofidou; Catherine Metaxotou; Emmanuel Kanavakis; Ariadni Mavrou
10 years' experience in fragile X testing among mentally retarded individuals in Greece: a molecular and epidemiological approach.
In vivo (Athens, Greece) 2008;22(4):451-5.
2008: Angeliki Galani; Sophia Kitsiou-Tzeli; Christalena Sofokleous; Emmanuel Kanavakis; Ariadni Kalpini-Mavrou
Androgen insensitivity syndrome: clinical features and molecular defects.
Hormones (Athens, Greece) 2008;7(3):217-29.
2008: Aspasia Tsezou; Maria Tzetis; Constantinos Gennatas; E Giannatou; A Pampanos; G Malamis; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli
Association of repeat polymorphisms in the estrogen receptors alpha, beta (ESR1, ESR2) and androgen receptor (AR) genes with the occurrence of breast cancer.
Breast (Edinburgh, Scotland) 2008;17(2):159-66.
2008: Carolina Sismani; Sophia Kitsiou-Tzeli; Marios Ioannides; Christodoulos Christodoulou; Violetta Anastasiadou; Goula Stylianidou; Eleftheria Papadopoulou; Emanuel Kanavakis; Zoe Kosmaidou-Aravidou; Philippos C Patsalis
Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype.
Molecular cytogenetics 2008;1():15.
2008: Katerina Salavoura; Aggeliki Kolialexi; C Sofocleous; M Kalaitzidaki; A Pampanos; Sophia Kitsiou-Tzeli; Ariadni Mavrou
Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndrome.
Genetic counseling (Geneva, Switzerland) 2008;19(2):219-24.
2008: Sophia Kitsiou-Tzeli; Carolina Sismani; George Koumbaris; Marios Ioannides; Emmanuel Kanavakis; Aggeliki Kolialexi; Ariadni Mavrou; Vassiliki Touliatou; Philippos C Patsalis
Distal del(4) (q33) syndrome: detailed clinical presentation and molecular description with array-CGH.
European journal of medical genetics 2008;51(1):61-7.
2007: Nikolaos Vogiatzakis; Kyriaki Kekou; Christalena Sophocleous; Sophia Kitsiou-Tzeli; Ariadni Mavrou; Chrisa Bakoula; Emmanuel Kanavakis
Screening human genes for small alterations performing an enzymatic cleavage mismatched analysis (ECMA) protocol.
Molecular biotechnology 2007;37(3):212-9.
2007: S Voutoufianakis; S Psoni; P Vorgia; F Tsekoura; Kyriaki Kekou; J Traeger-Synodinos; Sophia Kitsiou-Tzeli; E Kanavakis; Helen Fryssira
Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2007;11(4):235-9.
2007: Maria Moschovi; Vassiliki Touliatou; Touliatou Vassiliki; Anna Papadopoulou; Papadopoulou Anna; Maria-Alexandra Mayakou; Mayakou Maria-Alexandra; Polyxeni Nikolaidou-Karpathiou; Nikolaidou-Karpathiou Polyxeni; Sophia Kitsiou-Tzeli; Kitsiou-Tzeli Sophia
Rhabdomyosarcoma in a patient with Noonan syndrome phenotype and review of the literature.
Journal of pediatric hematology/oncology 2007;29(5):341-4.
2007: Aggeliki Kolialexi; George Th Tsangaris; A Anagnostopoulos; D Chondros; V Bagiokos; Sophia Kitsiou-Tzeli; Emmanuel Kanavakis; Ariadni Mavrou
Two-way trafficking of Annexin V positive cells between mother and fetus: determination of apoptosis at delivery.
Prenatal diagnosis 2007;27(4):348-51.
2007: Andreas Fretzayas; Sophia Kitsiou-Tzeli; Anna Papadopoulou; Polyxeni Nicolaidou
Clinical expression of co-inherited Dubin-Johnson and thalassaemic heterozygous states.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2007;39(4):369-74.
2007: Sophia Kitsiou-Tzeli; Eleanna Giannatou; I Spanos; Polyxeni Nicolaidou; Andreas Fretzayas; Maria Tzetis; Dimitrios Lazaris; Emmanuel Kanavakis; Aspasia Tsezou
Steroid hormones polymorphisms and cholelithiasis in Greek population.
Liver international : official journal of the International Association for the Study of the Liver 2007;27(1):61-8.
2007: Ariadni Mavrou; E Kouvidi; Aris Antsaklis; Athena P Souka; Sophia Kitsiou-Tzeli; Aggeliki Kolialexi
Identification of nucleated red blood cells in maternal circulation: a second step in screening for fetal aneuploidies and pregnancy complications.
Prenatal diagnosis 2007;27(2):150-3.
2007: Vassiliki Touliatou; Ariadni Mavrou; Aggeliki Kolialexi; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli
Saethre-Chotzen syndrome with severe developmental delay associated with deletion of chromosomic region 7p15 --> pter.
Genetic counseling (Geneva, Switzerland) 2007;18(3):295-301.
2007: Aspasia Tsezou; Maria Tzetis; Eirini Giannatou; Constantinos Gennatas; Andreas Pampanos; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli
Genetic polymorphisms in the UGT1A1 gene and breast cancer risk in Greek women.
Genetic testing 2007;11(3):303-6.
2007: Christina Kanaka-Gantenbein; Evangelos Papandreou; K Stefanaki; Helen Fryssira; Aggeliki Kolialexi; Christalena Sophocleous; Ariadni Mavrou; Sophia Kitsiou-Tzeli; George Chrousos
Spontaneous ovulation in a true hermaphrodite with normal male phenotype and a rare 46,XX/47,XXY Klinefelter's mosaic karyotype.
Hormone research 2007;68(3):139-44.
2007: Sophia Kitsiou-Tzeli; Carolina Sismani; Marios Ioannides; Stavros Bashiardes; Andria Ketoni; Vassiliki Touliatou; Aggeliki Kolialexi; Ariadni Mavrou; Emmanuel Kanavakis; Philippos C Patsalis
Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion.
European journal of medical genetics 2007;50(1):73-8.
2006: Aggeliki Kolialexi; Sophia Kitsiou-Tzeli; Helen Fryssira; C Sofocleous; E Kouvidi; George Th Tsangaris; Katerina Salavoura; Ariadni Mavrou
Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
In vivo (Athens, Greece) 2006;20(4):473-8.
2006: Sofia K Leka; Sophia Kitsiou-Tzeli; Ariadni Kalpini-Mavrou; Emmanuel Kanavakis
Short stature and dysmorphology associated with defects in the SHOX gene.
Hormones (Athens, Greece) 2006;5(2):107-18.
2006: Vassiliki Touliatou; Helen Fryssira; Ariadni Mavrou; Emmanuel Kanavakis; Sophia Kitsiou-Tzeli
Clinical manifestations in 17 Greek patients with Goldenhar syndrome.
Genetic counseling (Geneva, Switzerland) 2006;17(3):359-70.
2006: Katerina Salavoura; M Valari; Aggeliki Kolialexi; Ariadni Mavrou; Sophia Kitsiou-Tzeli
A case of Ehlers Danlos syndrome type VI.
Genetic counseling (Geneva, Switzerland) 2006;17(3):291-4.
2006: Sophia Kitsiou-Tzeli; Anna Papadopoulou; Christina Kanaka-Gantenbein; Andreas Fretzayas; Dimitris Daskalopoulos; Emmanuel Kanavakis; Polyxeni Nicolaidou
Does the rare A172G mutation of PTPN11 gene convey a mild Noonan syndrome phenotype?
Hormone research 2006;66(3):124-31.
2006: Andreas Fretzayas; Sophia Kitsiou-Tzeli; Aspasia Tsezou; Augustina Alexaki; Polyxeni Nicolaidou
UGT1A1 promoter polymorphism as a predisposing factor of hyperbilirubinaemia in neonates with acute pyelonephritis.
Scandinavian journal of infectious diseases 2006;38(6-7):537-40.
2006: Polyxeni Nicolaidou; Anna Papadopoulou; Helen Georgouli; Yiannis G Matsinos; Helen Tsapra; Andreas Fretzayas; Aglaia Giannoulia-Karantana; Sophia Kitsiou-Tzeli; Konstantinos Douros; Ioannis Papassotiriou; George Chrousos
Calcium and vitamin D metabolism in hypocalcemic vitamin D-resistant rickets carriers.
Hormone research 2006;65(2):83-8.
2005: Sophia Kitsiou-Tzeli; Aggeliki Kolialexi; Ariadni Mavrou
Endocrine manifestations in DiGeorge and other microdeletion syndromes related to 22q11.2.
Hormones (Athens, Greece) 2005;4(4):200-9.
2005: Polyxeni Nicolaidou; Stavroula Kostaridou; A Mavri; Angeliki Galla; Sophia Kitsiou-Tzeli; Alexandra Stamoulakatou
Glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome: a gene interaction underlies severe jaundice without severe hemolysis.
Pediatric hematology and oncology 2005;22(7):561-6.
2005: Aggeliki Kolialexi; George Th Tsangaris; Sophia Kitsiou-Tzeli; Emmanuel Kanavakis; Ariadni Mavrou
Impact of cytogenetic and molecular cytogenetic studies on hematologic malignancies.
Anticancer research 2005;25(4):2979-83.
2005: Philippos C Patsalis; Nicos Skordis; Carolina Sismani; Ludmila Kousoulidou; George Koumbaris; Christina Eftychi; George Stavrides; Antonis Ioulianos; Sophia Kitsiou-Tzeli; Angeliki Galla-Voumvouraki; Zoe Kosmaidou; Charalambos Hadjiathanasiou; Ken McElreavey
Identification of high frequency of Y chromosome deletions in patients with sex chromosome mosaicism and correlation with the clinical phenotype and Y-chromosome instability.
American journal of medical genetics. Part A 2005;135(2):145-9.
2005: Styliani Amenta; Christalena Sofocleous; Aggeliki Kolialexi; Loretta Thomaidis; Sotiris Giouroukos; Emmanuel Karavitakis; Ariadni Mavrou; Sophia Kitsiou-Tzeli; Emmanuel Kanavakis; Helen Fryssira
Clinical manifestations and molecular investigation of 50 patients with Williams syndrome in the Greek population.
Pediatric research 2005;57(6):789-95.
2004: Aggeliki Kolialexi; George Th Tsangaris; Aris Antsaklis; Sophia Kitsiou-Tzeli; Ariadni Mavrou
Use of annexin V for the identification of fetal cells in maternal circulation.
In vivo (Athens, Greece) 2004;18(5):629-32.
2004: Sophia Kitsiou-Tzeli; Aggeliki Kolialexi; Helen Fryssira; Angeliki Galla-Voumvouraki; Katerina Salavoura; Maria Kanariou; George Th Tsangaris; Emmanuel Kanavakis; Ariadni Mavrou
Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.
In vivo (Athens, Greece) 2004;18(5):603-8.
2004: Sophia Kitsiou-Tzeli; Aggeliki Kolialexi; Ariadni Mavrou
Mosaic Cri du Chat syndrome in a patient exhibiting three 5p cell lines.
Prenatal diagnosis 2004;24(7):578-9.
2004: Christina Kanaka-Gantenbein; Sophia Kitsiou-Tzeli; Ariadni Mavrou; Lela Stamoyannou; Aggeliki Kolialexi; Kyriaki Kekou; Magda Liakopoulou; George Chrousos
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.
Hormone research 2004;61(5):205-10.
2003: Sophia Kitsiou-Tzeli; Emmanuel Kanavakis; Maria Tzetis; Emmanuel Kavazarakis; Angeliki Galla; Aspasia Tsezou
Gilbert's syndrome as a predisposing factor for idiopathic cholelithiasis in children.
Haematologica 2003;88(10):1193-4.
2001: Maria Tzetis; Emmanuel Kanavakis; Aspasia Tsezou; Vasilios Ladis; E Pateraki; Theano P Georgakopoulou; Emmanuel Kavazarakis; E Maragoudaki; Themistocles Karpathios; Sophia Kitsiou-Tzeli
Gilbert syndrome associated with beta-thalassemia.
Pediatric hematology and oncology 2001;18(8):477-84.
2001: C Tsenghi; Sophia Kitsiou-Tzeli
Greece: the Hellenic Association of Medical Geneticists.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(3):221.
2001: Andreas Fretzayas; Maria Moustaki; Sophia Kitsiou-Tzeli; John Mathioudakis; Themistocles Karpathios
Splenic granulomatous lesions in immunocompetent pediatric patients with visceral leishmaniasis.
Scandinavian journal of infectious diseases 2001;33(11):865-7.
2000: Emmanuel Kavazarakis; Aspasia Tsezou; Maria Tzetis; A Hadjidimoula; Sophia Kitsiou-Tzeli; Emmanuel Kanavakis; Themistocles Karpathios
Gilbert syndrome: analysis of the promoter region of the uridine diphosphate-glucuronosyltransferase 1 gene in the Greek population.
European journal of pediatrics 2000;159(11):873-4.
2000: Aspasia Tsezou; Sophia Kitsiou-Tzeli; Angeliki Galla; Michael B Petersen; GEORGIA KARADIMA; Maria Syrrou; S Sahlèn; Elisabeth Blennow
Molecular cytogenetic characterization and origin of two de novo duplication 9p cases.
American journal of medical genetics 2000;91(2):102-6.
2000: Aspasia Tsezou; Maria Tzetis; Sophia Kitsiou-Tzeli; Emmanuel Kavazarakis; Angeliki Galla; Emmanuel Kanavakis
A Caucasian boy with Gilbert's syndrome heterozygous for the (TA)(8) allele.
Haematologica 2000;85(3):319.
1999: Aspasia Tsezou; Charalambos Hadjiathanasiou; Dimitrios Gourgiotis; Angeliki Galla; Emmanuel Kavazarakis; A Pasparaki; Manuela Kapsetaki; Carolina Sismani; Charalampos Theodoridis; Philippos C Patsalis; Nicholas K Moschonas; Sophia Kitsiou-Tzeli
Molecular genetics of Turner syndrome: correlation with clinical phenotype and response to growth hormone therapy.
Clinical genetics 1999;56(6):441-6.
1998: GEORGIA KARADIMA; Merete Bugge; P Nicolaidis; Dimitrios Vassilopoulos; Dimitrios Avramopoulos; Maria Grigoriadou; Beate Albrecht; Eberhard Passarge; Göran Annerén; Elisabeth Blennow; Niels Clausen; Angeliki Galla-Voumvouraki; Aspasia Tsezou; Sophia Kitsiou-Tzeli; Johanne M D Hahnemann; Jens Michael Hertz; Gunnar Houge; M Kuklík; Milan Macek Jr.; D Lacombe; K Miller; A Moncla; I López Pajares; Philippos C Patsalis; Michael B Petersen
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism.
European journal of human genetics : EJHG 1998;6(5):432-8.
1998: Nikolaos Papadopoulos; EK Papadaki; Sophia Kitsiou-Tzeli; Theologos Farmakakis; Andreas Fretzayas
A case of non-Fanconi anemia bone marrow dysfunction with familial involvement.
Pediatric hematology and oncology 1998;15(3):277-81.
1998: Philippos C Patsalis; Carolina Sismani; MI Hadjimarcou; Sophia Kitsiou-Tzeli; A Tzezou; Charalambos Hadjiathanasiou; Voula Velissariou; E Lymberatou; Nicholas K Moschonas; Nicos Skordis
Detection and incidence of cryptic Y chromosome sequences in Turner syndrome patients.
Clinical genetics 1998;53(4):249-57.
1998: Maria Syrrou; Ioannis Georgiou; Maria Grigoriadou; Michael B Petersen; Sophia Kitsiou-Tzeli; Gerassimos N Pagoulatos; Philippos C Patsalis
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population.
Genetic epidemiology 1998;15(1):103-9.
1997: Philippos C Patsalis; MI Hadjimarcou; Voula Velissariou; Sophia Kitsiou-Tzeli; C Zera; Maria Syrrou; E Lyberatou; Aspasia Tsezou; Angeliki Galla; Nicos Skordis
Supernumerary marker chromosomes (SMCs) in Turner syndrome are mostly derived from the Y chromosome.
Clinical genetics 1997;51(3):184-90.
1996: Aspasia Tsezou; Sophia Kitsiou-Tzeli; Angeliki Galla; Dimitrios Gourgiotis; IOANNIS PAPAGEORGIOU; S Mitrou; P A Molybdas; Konstantinos Sinaniotis
High nitrate content in drinking water: cytogenetic effects in exposed children.
Archives of environmental health 1996;51(6):458-61.
1996: Merete Bugge; Elisabeth Blennow; U Friedrich; Michael B Petersen; F Pedeutour; Aspasia Tsezou; A Orum; S Hermann; T Lyngbye; Catherine Sarri; Dimitrios Avramopoulos; Sophia Kitsiou-Tzeli; J C Lambert; M Guzda; Niels Tommerup; Karen Brøndum-Nielsen
Tetrasomy 18p de novo: parental origin and different mechanisms of formation.
European journal of human genetics : EJHG 1996;4(3):160-7.
1995: S Bajalica; Elisabeth Blennow; A Tşezou; A Galla-Voumvouraki; M Alevizaki; Konstantinos Sinaniotis; Sophia Kitsiou-Tzeli
Partial disomy of Xp and the presence of SRY in a phenotypic female.
Journal of medical genetics 1995;32(12):987-90.
1994: T D Apostolopoulos; Michael Kyriakidis; Sophia Kitsiou-Tzeli; A D Galla-Voumvouraki; Aspasia Tsezou; Pavlos K Toutouzas
45,X Turner syndrome with normal ovarial function and multiple malformations of the aorta.
Postgraduate medical journal 1994;70(829):838-40.
1994: Sophia Kitsiou-Tzeli; A Galla-Voumvouraki; Aspasia Tsezou; E Kavazarakis; A Skardoutsou; P Koukoutsakis; C Sinamniotis
Cytogenetic studies in children on long-term anticonvulsant therapy.
Acta paediatrica (Oslo, Norway : 1992) 1994;83(6):672-3.
1993: Aspasia Tsezou; Sophia Kitsiou-Tzeli; Helen Kosmidis; K Paidousi; K Katsouyanni; Konstantinos Sinaniotis
Constitutive heterochromatin polymorphisms in children with acute lymphoblastic leukemia.
Pediatric hematology and oncology 1993;10(1):7-11.
1992: Angeliki Galla; Sophia Kitsiou-Tzeli; Dimitrios Gourgiotis; E Hadjigeorgiou; H Yousef-Ayash; J Kanarios; K Richardson; Konstantinos Sinaniotis
Sister chromatid exchanges in peripheral lymphocytes in newborns treated with phototherapy and vitamin E.
Acta paediatrica (Oslo, Norway : 1992) 1992;81(10):820-3.
1988: Sophia Kitsiou-Tzeli; Photini Saxoni-Papageorgiou; T Haidemenaki; A Gala; P Koukoutsakis; C Stavrinadis; M Plassara; Konstantinos Sinaniotis
Sister chromatid exchanges in peripheral lymphocytes of children vaccinated against rubella and measles-mumps-rubella.
Acta paediatrica Scandinavica 1988;77(6):879-84.
1988: Sophia Kitsiou-Tzeli; M Siapera; J Amos; L Atkins; C S Bartsocas
[Polymorphism of restriction fragment length in the detection of the precise status of monosomy 21 in a deformed retarded girl].
Journal de génétique humaine 1988;36(1-2):99-102.
1987: Ariadne Malamitsi-Puchner; Sophia Kitsiou-Tzeli; Christos S Bartsocas
Severe proteus syndrome in an 18-month-old boy.
American journal of medical genetics 1987;27(1):119-25.
1987: Sophia Kitsiou-Tzeli; Aspasia Tsezou; C S Bartsocas; P Tapratzi; G Kourakis; C Papas; H Dellagrammaticas
Complex chromosome rearrangement in a retarded girl with malformations.
Annales de génétique 1987;30(1):59-61.
1986: Sophia Kitsiou-Tzeli; C S Bartsocas; D Alexiou; D Mourtzinis
Unusual pathologic findings in a girl with Wolf-Hirschhorn syndrome, del (4p).
Pediatric pathology / affiliated with the International Paediatric Pathology Association 1986;6(2-3):161-5.
1986: Sophia Kitsiou-Tzeli; C S Bartsocas
Unusual association of XYY chromosomal constitution with colobomas of iris, myopia, increased lipoproteins, mental retardation and convulsions.
Annales de génétique 1986;29(4):264-5.
1985: S E Antonarakis; S D Kittur; C Metaxotou; C Bartsocas; Sophia Kitsiou-Tzeli; P C Watkins; A S Patel; AC Warren; James Gusella; Y Groner
Linkage map on chromosome 21q and the association of a DNA haplotype with a propensity to nondisjunction and trisomy 21.
Annals of the New York Academy of Sciences 1985;450():95-107.
1984: Sophia Kitsiou-Tzeli; J J Hallett; L Atkins; S A Latt; L B Holmes
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.
American journal of medical genetics 1984;18(4):725-9.
1983: Sophia Kitsiou-Tzeli; H D Dellagrammaticas; C B Papas; I D Ladas; C S Bartsocas
Unusual ocular findings in an infant with cri-du-chat syndrome.
Journal of medical genetics 1983;20(4):304-7.
1979: E Hadjigeorgiou; Sophia Kitsiou-Tzeli; A Psaroudakis; C Segos; D Nicolopoulos; D Kaskarelis
Antepartum aminophylline treatment for prevention of the respiratory distress syndrome in premature infants.
American journal of obstetrics and gynecology 1979;135(2):257-60.
1978: D A Kafetzis; Konstantinos Sinaniotis; Sophia Kitsiou-Tzeli; C J Papadatos
Tobramycin dosage in infants and children.
Lancet 1978;2(8102):1264.