Zobrazeno 1 - 10
of 176
pro vyhledávání: '"Thomaidis L"'
Publikováno v:
Neuropsychiatric Disease and Treatment, Vol Volume 12, Pp 3093-3095 (2016)
Loretta Thomaidis, Antigoni Choleva, Miltiades Kyprianou Second Department of Paediatrics, Developmental Assessment Unit, “P. & A. Kyriakou” Children’s Hospital, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece
Externí odkaz:
https://doaj.org/article/4145557cd1ee4bde99309dc4ec393c87
Backround: This systematic review aims to examine the associations between features of gut microbiome and Attention Deficit/Hyperactivity Disorder (ADHD) risk or severity in children, adolescents and young adults. Methods: Eligible studies were ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::e5d73e9c51b23d325529c4d5cab32c84
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3220986
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3220986
OBJECTIVE: This paper aims to study the views, perceptions and representations of online hate speech among adolescents in the Greek cohort of the SELMA Project. METHODS: Qualitative research was conducted in focus groups of 36 Greek adolescents and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::3d51f22157ceedd09ec87f933c584350
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3119429
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3119429
Background: overweight and obese individuals may often face aggressive messages or comments on the internet. This study attempts to evaluate the association between cyberbullying victimization and overweight/obesity in adolescents participating in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::3fc488b59c687af99c1acdf3ccdf6e85
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3102673
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3102673
Autism spectrum disorders (ASD) constitute a public health concern with increasing prevalence worldwide. We aimed to estimate prevalence and age at diagnosis in Greece, where no large-scale prevalence study has ever been conducted. Aggregate data wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c768769355ea0c849fbce2f2bb8339be
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3104177
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3104177
To date, 6 cases of 17p13.1 microduplications have been described in the literature. Intellectual disability is the core feature, together with minor facial dysmorphisms and obesity. We describe the first case of a young patient with a maternally inh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::9c2e85accdcc3bd0d74bb8f0c1cd8666
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078904
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3078904
In this report, a patient carrying a 650 kb deletion and a 759 kb duplication of chromosomal 21q22.3 region was described. Facial dysmorphic features, hypotonia, short stature, learning impairment, autism spectrum disorder, anxiety and depression wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::6541b30cc614d511dbb7149cd64b2bcc
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997797
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2997797
Background: Short arm deletions of the X-chromosome are challenging issues for genetic counseling due to their low penetrance in population. Female carriers of these deletions have milder phenotype than male ones, considering the intellectual ability
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::be43772ac7cd065552d249da3f68da09
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3087069
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3087069
Long-term follow-up of a child with Klinefelter syndrome and achondroplasia from infancy to 16 years
Background: Achondroplasia (ACH), an autosomal dominant skeletal dysplasia, occurs in approximately 1:20,000 births. On the other hand, 47,XXY aneuploidy (Klinefelter syndrome [KS]) is the most common sex chromosome disorder, with a prevalence of app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::050afdd7e3d0976821bc30094a21207f
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3087370
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3087370