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Language acquisition: Hesitations in the question/answer dialogic pair
(2015-01-01)
Purpose: (1) To verify the existence (or not) of hesitation marks in the beginning of utterances in children's discourse; and (2) to determine to what extent the presence/absence of these marks could be explained by ...
Preschoolers' performance on the brazilian adaptation of the preschool language assessment instrument - Second edition
(2016-10-01)
Purpose: The objective was to test whether the Brazilian version of the Preschool Language Assessment Instrument - Second Edition (PLAI-2) has the potential to assess and identify differences in typical language development ...
Issues of language and literacy revisited
(School of Education, UWI, St. Augustine, 2008)
This paper reviews the present state of academic and medical knowledge on the problems that children encounter in acquiring both language and literacy, and concludes that we need to face the issues on other fronts than ...
Diretrizes para a saúde da criança: o desenvolvimento da linguagem em focoGuidelines for child health: language development on focus
(Associação Brasileira de Saúde Coletiva, 2020)
Bilinguismo infantil: uma análise do comportamento linguístico de uma criança bilíngue brasileira em interações familiares
(Universidade do Vale do Rio dos Sinos, 2016)
Currently, It has been noticed, many parents would like to raise bilingual kids since the very first days of life; meanwhile, they show quite uncertainness about this subject and if it can confuse the child in the languages’ ...
Bilinguismo infantil: uma análise do comportamento linguístico de uma criança bilíngue brasileira em interações familiares
(Universidade do Vale do Rio dos Sinos, 2016)
Currently, It has been noticed, many parents would like to raise bilingual kids since the very first days of life; meanwhile, they show quite uncertainness about this subject and if it can confuse the child in the languages’ ...
Language, behavior and neurodevelopment in Joubert syndrome: A case report
(2016-01-01)
The Joubert syndrome (JS) is a rare, heterogeneous genetic condition among the ciliopathies. More than 20 genes have been identified associated with this phenotype. The main manifestations include hypotonia, ataxia, ...