2010
DOI: 10.1016/j.rasd.2010.01.004
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The neurobiology of autism: Theoretical applications

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Cited by 30 publications
(12 citation statements)
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“…Kientz and Dunn 1997; Watling et al 2001; Ben-Sasson et al 2007; Tomcheck and Dunn 2007; Baker et al 2008; Hilton et al 2010), neurobiological deficits (e.g. Gillberg 1999; Bauman and Kemper 2005; Schroeder et al 2010), specific deficits in the capacity to feel and integrate emotions (e.g. Capps et al 1992; Leekam 2005), or to motor or facial expression deficits (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…Kientz and Dunn 1997; Watling et al 2001; Ben-Sasson et al 2007; Tomcheck and Dunn 2007; Baker et al 2008; Hilton et al 2010), neurobiological deficits (e.g. Gillberg 1999; Bauman and Kemper 2005; Schroeder et al 2010), specific deficits in the capacity to feel and integrate emotions (e.g. Capps et al 1992; Leekam 2005), or to motor or facial expression deficits (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…It is characterized by social impairments, deficits in communication, and restricted and repetitive behavior (Rippon et al, 2007;Schroeder et al, 2010). These symptoms begin normally before a child is about three (2-4) years old (Courchesne et al, 2004;Redcay and Courchesne, 2005;Klin et al, 2009).…”
Section: Introductionmentioning
confidence: 99%
“…There are several cognitive theories and models of core deficits of autism such as theory of mind deficit, executive dysfunction and the mirror neuron system model, and the weak central coherence that are not completely accepted or unified yet (Rajendran and Mitchell, 2007), although some attempts have been made in order to unify them (Schroeder et al, 2010). Also, many regions are known to be affected in autistic brain, such as social brain (amygdala, medial prefrontal cortex, and posterior superior temporal sulcus), executive functions (primarily frontal cortex) (Rippon et al, 2007;Chan et al, 2009), and brainstem (Galbraith, 2008) but its sources and how it occurs is not completely understood.…”
Section: Introductionmentioning
confidence: 99%
“…Se forem utilizados os critérios aceitos pela Organização Mundial de Saúde (CID, atualmente na décima edição) 12 ou pela Associação Americana de Psiquiatria (DSM, atualmente na quarta edição) 13 , esse, certamente, não é um distúrbio raro 3 . A incidência de TEA tem aumentado de forma significativa em todo o mundo 14 . O TEA ocupa o terceiro lugar entre os distúrbios do desenvolvimento, estando à frente das malformações congênitas e da síndrome de Down 3 .…”
unclassified
“…A reavaliação para características mais abrangentes, como déficits em comunicação e alterações sociais, faz com que essa concordância aumente de 60% para 92% em monozigóticos e de 0% para 10% em dizigóticos 22 . Extensas investigações revelaram o envolvimento de diferentes áreas encefálicas na gênese do TEA, incluindo estruturas do sistema límbico, amígdala, áreas pré-frontais e cerebelo 14,15,23 . As anormalidades poderiam ser induzidas em múltiplos períodos pré-natais, especialmente nas regiões cerebrais que se desenvolvem tardiamente na neurogênese.…”
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