A. Mavrou

发表

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

S. Gagos, C. Sofocleous, S. Zachaki, 2020, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

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

E. Kanavakis, S. Zachaki, K. Manola, 2020, In Vivo.

The normal human amniotic fluid supernatant proteome.

G. Tsangaris, M. Fountoulakis, A. Anagnostopoulos, 2006, In vivo.

Efficiency of interphase fluorescence in situ hybridization for BCR/ABL on peripheral blood smears for monitoring of CML patients: a comparison with bone marrow findings.

S. Akel, D. Loukopoulos, X. Yataganas, 2002, Clinical and laboratory haematology.

Evaluation at single cell level of residual Philadelphia negative hemopoietic stem cells in chronic phase CML patients.

S. Akel, D. Loukopoulos, X. Yataganas, 2000, Cancer genetics and cytogenetics.

Application of proteomics for the identification of biomarkers in amniotic fluid: are we ready to provide a reliable prediction?

G. Tsangaris, A. Anagnostopoulos, A. Antsaklis, 2011, EPMA Journal.

Dysregulated placental microRNAs in Early and Late onset Preeclampsia.

M. Tzetis, G. Lambrou, C. Siristatidis, 2018, Placenta.

Proteomic analysis of human reproductive fluids

G. Tsangaris, A. Kolialexi, A. Mavrou, 2007, Proteomics. Clinical applications.

Early Identification of Women at Risk of Gestation Diabetes Mellitus

A. Mavrou, Danay Mavreli, 2017 .

Urine proteomic studies in preeclampsia

Danai Mavreli, N. Papantoniou, A. Kolialexi, 2015, Proteomics. Clinical applications.

Coffin-Siris Syndrome 4-Related Spectrum in a Young Woman Caused by a Heterozygous SMARCA4 Deletion Detected by High-Resolution aCGH

M. Tzetis, E. Kanavakis, L. Lazaros, 2020, Molecular Syndromology.

Application of proteomics for the identification of differentially expressed protein markers for Down syndrome in maternal plasma

G. Tsangaris, A. Anagnostopoulos, A. Antsaklis, 2008, Prenatal diagnosis.

Proteomic analysis of amniotic fluid in pregnancies with Klinefelter syndrome foetuses.

G. Tsangaris, E. Kanavakis, M. Fountoulakis, 2010, Journal of proteomics.

Association of A313G glutathione S-transferase P1 germline polymorphism with susceptibility to de novo myelodysplastic syndrome

E. Kanavakis, G. Pantelias, T. Koromila, 2013, Leukemia & lymphoma.

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

E. Kanavakis, C. Sofocleous, H. Fryssira, 2005, Pediatric Research.

Non-invasive prenatal diagnosis using cell-free fetal nucleic acids in maternal plasma: Progress overview beyond predictive and personalized diagnosis

G. Tsangaris, E. Kanavakis, N. Papantoniou, 2011, EPMA Journal.

Clinical manifestations in 17 Greek patients with Goldenhar syndrome.

E. Kanavakis, S. Kitsiou-Tzeli, H. Fryssira, 2006, Genetic counseling.

Endocrine manifestations in DiGeorge and other microdeletion syndromes related to 22q11.2.

S. Kitsiou‐Tzeli, A. Kolialexi, A. Mavrou, 2005, Hormones.

Improved Specificity of NRBC Detection in Chorionic Villus Sample Supernatant Fluids Using Anti-Zeta and Anti-Epsilon Monoclonal Antibodies

Yun-Ling Zheng, D. Bianchi, A. Mavrou, 1999, Fetal Diagnosis and Therapy.

Screening of UBE3A gene in patients referred for Angelman Syndrome.

S. Kitsiou‐Tzeli, E. Kanavakis, C. Sofocleous, 2013, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Validation of Serum Biomarkers Derived from Proteomic Analysis for the Early Screening of Preeclampsia

G. Daskalakis, Danai Mavreli, A. Lykoudi, 2015, Disease markers.

A clinical study of Sotos syndrome patients with review of the literature.

E. Kanavakis, S. Kitsiou-Tzeli, H. Fryssira, 2009, Pediatric neurology.

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

G. Chrousos, C. Kanaka-Gantenbein, S. Kitsiou, 2004, Hormone Research in Paediatrics.

Apoptosis in maternal peripheral blood during pregnancy

G. Tsangaris, F. Tzortzatou, A. Mavrou, 1998, Pediatric Research.

Proteomic analysis of amniotic fluid for the diagnosis of fetal aneuploidies

G. Tsangaris, A. Kolialexi, A. Mavrou, 2011, Expert review of proteomics.

Proteomic analysis of amniotic fluid in pregnancies with Turner syndrome fetuses.

G. Tsangaris, M. Fountoulakis, A. Anagnostopoulos, 2008, Journal of proteome research.

Proteomic analysis of amniotic fluid in pregnancies with Down syndrome

G. Tsangaris, M. Fountoulakis, S. Garbis, 2006, Proteomics.

RASSF1A in maternal plasma as a molecular marker of preeclampsia

E. Kanavakis, A. Antsaklis, N. Papantoniou, 2013, Prenatal diagnosis.

Use of annexin V for the identification of fetal cells in maternal circulation.

S. Kitsiou‐Tzeli, G. Tsangaris, A. Antsaklis, 2004, In vivo.

Workshop report on the extraction of foetal DNA from maternal plasma

F. Crea, M. Sprenger-Haussels, D. Maddocks, 2007, Prenatal diagnosis.

Application of proteomics for diagnosis of fetal aneuploidies and pregnancy complications.

G. Tsangaris, A. Anagnostopoulos, A. Kolialexi, 2009, Journal of proteomics.

Proteomics in prenatal diagnosis

G. Tsangaris, A. Kolialexi, A. Mavrou, 2009, Expert review of proteomics.

Plasma biomarkers for the identification of women at risk for early-onset preeclampsia

G. Tsangaris, S. Sifakis, D. Gourgiotis, 2017, Expert review of proteomics.

Collyria seals in the Roman Empire.

D. Piñero, A. Cerviño, R. Brautaset, 2013, Acta medico-historica adriatica : AMHA.

A 46,XX Karyotype in Men with Infertility: Two New Cases and Review of the Literature

E. Kanavakis, S. Zachaki, K. Manola, 2022, Journal of human reproductive sciences.

Spontaneous Ovulation in a True Hermaphrodite with Normal Male Phenotype and a Rare 46,XX/47,XXY Klinefelter’s Mosaic Karyotype

G. Chrousos, C. Kanaka-Gantenbein, H. Fryssira, 2007, Hormone Research in Paediatrics.

Fetal nucleated erythrocytes (NRBCS) in chorionic villus sample supernatant fluids: an additional source of fetal material for karyotype confirmation

Yun-Ling Zheng, D. Bianchi, A. Mavrou, 1997, Prenatal diagnosis.

Deletion patterns of Duchenne and Becker muscular dystrophies in Greece.

A. Mavrou, K. Kekou, L. Florentin, 1995, Journal of medical genetics.

miRNAs in pregnancy-related complications

Danai Mavreli, N. Papantoniou, A. Kolialexi, 2015, Expert review of molecular diagnostics.

The ATM gene and ataxia telangiectasia.

G. Tsangaris, A. Kolialexi, A. Mavrou, 2008, Anticancer research.

Awareness and use of prenatal diagnosis among Greek women: a national survey

A. Mavrou, D. Trichopoulos, C. Metaxotou, 1998, Prenatal diagnosis.

The impact of preimplantation genetic testing for aneuploidies (PGT-A) on clinical outcomes in high risk patients

M. Koutsilieris, M. Tzetis, E. Kanavakis, 2022, Journal of Assisted Reproduction and Genetics.

Distal del(4) (q33) syndrome: detailed clinical presentation and molecular description with array-CGH.

C. Sismani, S. Kitsiou‐Tzeli, E. Kanavakis, 2008, European journal of medical genetics.

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

S. Kitsiou, N. Vogiatzakis, A. Mavrou, 2007, Molecular Biotechnology.

Identification of nucleated red blood cells in maternal circulation: A second step in screening for fetal aneuploidies and pregnancy complications

A. Souka, A. Antsaklis, A. Kolialexi, 2007, Prenatal diagnosis.

Unilateral microtia in an infant with trisomy 18 mosaicism.

A. Kolialexi, A. Mavrou, E. Giannatou, 2009, Genetic counseling.

Biomarker development for non-invasive prenatal diagnosis of fetal aneuploidies: predictive reliability and potential clinical application

G. Tsangaris, A. Anagnostopoulos, A. Antsaklis, 2011, EPMA Journal.

Potential biomarkers for Turner in maternal plasma: possibility for noninvasive prenatal diagnosis.

G. Tsangaris, M. Fountoulakis, A. Anagnostopoulos, 2010, Journal of proteome research.

Jérôme Lejeune (1926-1994): father of modern genetics.

E. Petridou, M. Karamanou, G. Androutsos, 2012, Acta medico-historica adriatica : AMHA.

Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in Greece.

M. Syrrou, A. Mavrou, C. Metaxotou, 1991, American journal of medical genetics.

Molecular diagnosis of Fragile X syndrome

C. Sofocleous, A. Kolialexi, A. Mavrou, 2009, Expert review of molecular diagnostics.

Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion.

C. Sismani, S. Kitsiou‐Tzeli, P. Patsalis, 2007, European journal of medical genetics.

Mapping dystrophin gene recombinants in Greek DMD/BMD families: low recombination frequencies in the STR region

A. Mavrou, K. Kekou, L. Florentin, 1995, Human Genetics.

Prenatal diagnosis of chromosomal abnormalities from chorionic biopsy samples: Improved success rate using a modified direct method

P. Panagiotopoulou, A. Antsaklis, A. Mavrou, 1987, Prenatal diagnosis.

Identification of Fetal Nucleated Red Blood Cells in the Maternal Circulation during Pregnancy Using Anti-Hemoglobin-ε Antibody

A. Antsaklis, A. Kolialexi, A. Mavrou, 2003, Fetal Diagnosis and Therapy.

Development of cancer in patients with primary immunodeficiencies.

Ariadni Mavrou, G. Tsangaris, A. Kolialexi, 2008, Anticancer research.

Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patient.

M. Syrrou, S. Youroukos, A. Mavrou, 1988, American journal of medical genetics.

Three Novel Mutations in Greek Sotos Patients with Rare Clinical Manifestations

E. Kanavakis, P. Willems, H. Fryssira, 2008, Hormone Research in Paediatrics.

The Growth Pattern and Final Height of Girls With Turner Syndrome With and Without Human Growth Hormone Treatment

N. Georgopoulos, C. Dacou-voutetakis, A. Mavrou, 1998, Pediatrics.

Screening for minor changes in the distal part of the human dystrophin gene in Greek DMD/BMD patients

S. Youroukos, A. Mavrou, H. Skouteli, 1999, European Journal of Human Genetics.

A familial X/Y translocation in a boy with ichthyosis, hypogonadism and mental retardation

M. Alevizaki, P. Panagiotopoulou, D. Ikkos, 1983, Clinical genetics.

Non-Hodgkin lymphoma in a child with Williams syndrome.

M. Moschovi, C. Sofocleous, H. Fryssira, 2004, Cancer genetics and cytogenetics.

Mass spectrometry-based proteomics in reproductive medicine.

G. Spyrou, G. Tsangaris, A. Kolialexi, 2008, Mass spectrometry reviews.

Use of Annexin V Antibody to Identify Apoptotic Cells during Pregnancy

G. Tsangaris, A. Antsaklis, A. Mavrou, 2001, Annals of the New York Academy of Sciences.

Noninvasive fetal RhD genotyping from maternal blood

A. Kolialexi, A. Mavrou, G. Tounta, 2010, Expert review of molecular diagnostics.

Investigation of FANCA mutations in Greek patients.

C. Sofocleous, S. Kitsiou, A. Kattamis, 2013, Anticancer research.

The Protein Profile of the Human Immature T-cell Line CCRF-CEM.

Konstantinos Vougas, Ariadni Mavrou, G. Tsangaris, 2005, Cancer genomics & proteomics.

PLACENTAL MICRORNAS IN EARLY AND LATE ONSET PREECLAMPSIA 1 2

Charalampos, M. Tzetis, G. Lambrou, 2018 .

A multiplex PCR for non-invasive fetal RHD genotyping using cell-free fetal DNA.

G. Tsangaris, E. Kanavakis, C. Vrettou, 2011, In vivo.

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

M. Tzetis, S. Zachaki, L. Lazaros, 2018, Balkan Journal of Medical Genetics.

Fetal cells in maternal plasma are found in a late state of apoptosis

G. Tsangaris, A. Antsaklis, A. Kolialexi, 2004, Prenatal diagnosis.

Identification of fetal nucleated red blood cells in the maternal circulation during pregnancy using anti-hemoglobin-epsilon antibody.

A. Antsaklis, A. Kolialexi, A. Mavrou, 2003, Fetal diagnosis and therapy.

Fetal cells in maternal blood: isolation by magnetic cell sorting and confirmation by immunophenotyping and FISH.

G. Tsangaris, P. Panagiotopoulou, A. Antsaklis, 1998, In vivo.

Early non-invasive detection of fetal Y chromosome sequences in maternal plasma using multiplex PCR.

E. Kanavakis, C. Vrettou, A. Antsaklis, 2012, European journal of obstetrics, gynecology, and reproductive biology.

Facioscapulohumeral muscular dystrophy molecular testing using a non radioactive protocol.

H. Fryssira, P. Manta, A. Mavrou, 2005, Molecular and cellular probes.

Detection of 22q11.2 deletion among 139 patients with Di George/Velocardiofacial syndrome features.

G. Tsangaris, E. Kanavakis, S. Kitsiou-Tzeli, 2004, In vivo.

Noninvasive prenatal diagnosis of β‐thalassaemia using individual fetal erythroblasts isolated from maternal blood after enrichment

R. Burgemeister, J. Traeger-Synodinos, E. Kanavakis, 2007 .

Impact of cytogenetic and molecular cytogenetic studies on hematologic malignancies.

G. Tsangaris, E. Kanavakis, A. Mavrou, 2005, Anticancer research.

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

S. Kitsiou, N. Vogiatzakis, A. Mavrou, 2007, Molecular biotechnology.

First-trimester NRBC Count in Maternal Circulation: Correlation with Doppler Ultrasound Studies

E. Kanavakis, P. Antsaklis, A. Antsaklis, 2005, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.