Results 131 to 140 of about 151,690 (300)
Includes abstract.Includes bibliographical references (leaves 92-96).Working from the transfer-inappropriate processing shift (Schooler, 2002), this project aimed to investigate whether a shift from automatic to controlled processing would impair face ...
Nortje, Alicia
core
Computer generated characters are now commonplace in television and film. In some media productions like the Matrix™ they feature as frequently as the real cast.
D Ballin +5 more
core
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli +18 more
wiley +1 more source
The authors report data from a longitudinal study that addresses the relations between working memory capacity and reading comprehension skills in children aged 8, 9, and 11 years.
Bryant, P. E. +8 more
core
Meta-language problems of artistic education
Trying to create the discribing language of non verbal component of communication we sent to find the solution of the similar problem relevant to an imagine component.
V.I. Mordan
doaj
ABSTRACT Bardet–Biedl syndrome (BBS) is a rare genetic condition with a broad phenotypic spectrum. Knowledge about quality of life, executive functioning, and eating behavior in adults with BBS remains limited. This study aimed to assess health‐related quality of life (HRQoL), everyday executive functioning, and eating behavior in adults with BBS and ...
Cecilie Fremstad Rustad +6 more
wiley +1 more source
Verbal and nonverbal components in the language system
The present article is devoted to the special role of nonverbal means in communication. It reveals the function of the latter in the language system. The author offers a system linguistic approach to the differentiation between linguistics and paralinguistics, proves the idea, that a considerable amount of paralinguistic phenomena, e.g. descriptive and
openaire +1 more source
Streamlining Diagnosis of Bardet–Biedl Syndrome: New Diagnostic Algorithm With Updated Criteria
ABSTRACT Considerable advances have been made in our understanding of Bardet–Biedl syndrome (BBS), particularly in its core clinical features and molecular genetics, warranting an update to the existing diagnostic criteria framework. Using a rigorous, evidence‐based, and consensus‐driven process, a multidisciplinary group of international experts and ...
Jeremy J. Pomeroy +16 more
wiley +1 more source
ABSTRACT DNM1 encephalopathy is a rare autosomal dominant genetic condition characterized by a range of neurological and developmental manifestations. The typical phenotype is severe, including profound intellectual disability, treatment‐resistant epilepsy, ataxia, and structural brain abnormalities. However, milder presentations have increasingly been
Caroline Crain +6 more
wiley +1 more source
ABSTRACT Women with the FMR1 premutation (PM) are at increased risk for fragile X‐associated conditions (FXPAC), including cognitive and psychiatric features collectively termed fragile X‐associated neuropsychiatric disorders (FXAND). This study is the first to systematically investigate cognitive and psychiatric features in Italian female premutation ...
Federica Alice Maria Montanaro +5 more
wiley +1 more source

