Results 131 to 140 of about 151,690 (300)

Face off : automatic versus controlled processing: does a shift in processing affect facial recognition?

open access: yes, 2011
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  

A Framework For Interpersonal Attitude And Non-Verbal Communication In Improvisational Visual Media Production

open access: yes, 2004
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  

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

Children's reading comprehension ability: Concurrent prediction by working memory, verbal ability, and component skills.

open access: yes, 2004
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

open access: yesОсвітній вимір, 2009
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  

Health‐Related Quality of Life, Everyday Executive Functioning, and Eating Behavior in Adults With Bardet–Biedl Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

open access: yesRUDN Journal of Philosophy, 2015
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

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

Refining Domain‐Based Prognostication in DNM1 Encephalopathy: A Mild Phenotype Associated With a GTPase Domain Variant

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
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

Psychiatric and Cognitive Features in Italian Women With the FMR1 Premutation: A Comprehensive Assessment Using SCID‐5 and Standardized Cognitive Measures

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
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

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