Age-related issues of instruments screening for autism in young children

por Thomaidis, Loretta, Choleva, Antigoni, Kyprianou, Miltiades
Publicado 2016

Cognitive and psychosocial development of HIV pediatric patients receiving highly active anti-retroviral therapy: a case-control study

por Thomaidis, Loretta, Bertou, Georgia, Critselis, Elena, Spoulou, Vassiliki, Kafetzis, Dimitrios A, Theodoridou, Maria
Publicado 2010

Predictors of severity and outcome of global developmental delay without definitive etiologic yield: a prospective observational study

por Thomaidis, Loretta, Zantopoulos, Georgios Zacharias, Fouzas, Sotirios, Mantagou, Lito, Bakoula, Chryssa, Konstantopoulos, Andreas
Publicado 2014

Autism Spectrum Disorders in Greece: Nationwide Prevalence in 10–11 Year-Old Children and Regional Disparities

por Thomaidis, Loretta, Mavroeidi, Nikoletta, Richardson, Clive, Choleva, Antigoni, Damianos, George, Bolias, Konstantinos, Tsolia, Maria
Publicado 2020

Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities

por Dagklis, Themistoklis, Papageorgiou, Elena, Siomou, Elisavet, Paspaliaris, Vassilis, Zerva, Christina, Chatzis, Panagiotis, Thomaidis, Loretta, Manolakos, Emmanouil, Papoulidis, Ioannis
Publicado 2016

Proximal 10q duplication in a child with severe central hypotonia characterized by array-comparative genomic hybridization: A case report and review of the literature

por MANOLAKOS, EMMANOUIL, VETRO, ANNALISA, GARAS, ANTONIOS, THOMAIDIS, LORETTA, KEFALAS, KONSTANTINOS, KITSOS, GEORGE, ZIEGLER, MONIKA, LIEHR, THOMAS, ZUFFARDI, ORSETTA, PAPOULIDIS, IOANNIS
Publicado 2014

Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male

por Papoulidis, Ioannis, Paspaliaris, Vassilis, Siomou, Elisavet, Orru, Sandro, Murru, Roberta, Sifakis, Stavros, Nikolaidis, Petros, Garas, Antonios, Sotiriou, Sotirios, Thomaidis, Loretta, Manolakos, Emmanouil
Publicado 2015

A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization

por Papoulidis, Ioannis, Vetro, Annalisa, Paspaliaris, Vassilis, Ziegler, Monika, Kreskowski, Katharina, Daskalakis, George, Papadopoulos, Vasilios, Dagklis, Themistoklis, Liehr, Thomas, Thomaidis, Loretta, Manolakos, Emmanouil
Publicado 2018

A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics

por Lagou, Magdalini, Papoulidis, Ioannis, Orru, Sandro, Papadopoulos, Vasileios, Daskalakis, George, Kontodiou, Maria, Anastasakis, Eleftherios, Petersen, Michael B, Kitsos, George, Thomaidis, Loretta, Manolakos, Emmanouil
Publicado 2014

Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search

por Vrachnis, Nikolaos, Papoulidis, Ioannis, Vrachnis, Dionysios, Siomou, Elisavet, Antonakopoulos, Nikolaos, Oikonomou, Stavroula, Zygouris, Dimitrios, Loukas, Nikolaos, Iliodromiti, Zoi, Pavlidou, Efterpi, Thomaidis, Loretta, Manolakos, Emmanouil
Publicado 2021

Cyberbullying and Obesity in Adolescents: Prevalence and Associations in Seven European Countries of the EU NET ADB Survey

por Sergentanis, Theodoros N., Bampalitsa, Sofia D., Theofilou, Paraskevi, Panagouli, Eleni, Vlachopapadopoulou, Elpis, Michalacos, Stefanos, Gryparis, Alexandros, Thomaidis, Loretta, Psaltopoulou, Theodora, Tsolia, Maria, Bacopoulou, Flora, Tsitsika, Artemis
Publicado 2021

Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)

por Manolakos, Emmanouil, Orru, Sandro, Neroutsou, Rosita, Kefalas, Konstantinos, Louizou, Eirini, Papoulidis, Ioannis, Thomaidis, Loretta, Peitsidis, Panagiotis, Sotiriou, Sotirios, Kitsos, George, Tsoplou, Panagiota, Petersen, Michael B, Metaxotou, Aikaterini
Publicado 2009

Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization

por Papadopoulou, Zoe, Papoulidis, Ioannis, Sifakis, Stavros, Markopoulos, Georgios, Vetro, Annalisa, Vlaikou, Angeliki-Maria, Ziegler, Monica, Liehr, Thomas, Thomaidis, Loretta, Zuffardi, Orsetta, Syrrou, Maria, George, Kitsos, Manolakos, Emmanouil
Publicado 2017

Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH

por Manolakos, Emmanouil, Kefalas, Konstantinos, Vetro, Annalisa, Oikonomidou, Eirini, Daskalakis, George, Psara, Natasa, Siomou, Elisa, Papageorgiou, Elena, Sevastopoulou, Eirini, Konstantinidou, Anastasia, Vrachnis, Nikolaos, Thomaidis, Loretta, Zuffardi, Orsetta, Papoulidis, Ioannis
Publicado 2013

The use of array-CGH in a cohort of Greek children with developmental delay

por Manolakos, Emmanouil, Vetro, Annalisa, Kefalas, Konstantinos, Rapti, Stamatia-Maria, Louizou, Eirini, Garas, Antonios, Kitsos, George, Vasileiadis, Lefteris, Tsoplou, Panagiota, Eleftheriades, Makarios, Peitsidis, Panagiotis, Orru, Sandro, Liehr, Thomas, Petersen, Michael B, Thomaidis, Loretta
Publicado 2010