Literatura científica selecionada sobre o tema "Déficits auditifs centraux"
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Artigos de revistas sobre o assunto "Déficits auditifs centraux"
Matas, Carla Gentile, Isabela Crivellaro Gonçalves, Fernanda Cristina Leite Magliaro, Renata Aparecida Leite e Laura Maria de Figueiredo Ferreira Guilhoto. "Avaliação audiológica e eletrofisiológica da audição na síndrome de Landau-Kleffner". Revista da Sociedade Brasileira de Fonoaudiologia 12, n.º 2 (junho de 2007): 79–85. http://dx.doi.org/10.1590/s1516-80342007000200003.
Texto completo da fonteRegatos Corchete, Gema. "Propuesta de innovación: programa de intervención centrada en soluciones con el alumnado de logopedia de la UPSA para el desarrollo exitoso de competencias profesionales en el manejo de pacientes con implante coclear". Revista INFAD de Psicología. International Journal of Developmental and Educational Psychology. 2, n.º 1 (16 de julho de 2022): 57–62. http://dx.doi.org/10.17060/ijodaep.2022.n1.v2.2315.
Texto completo da fonteAto Lozano, Ester, Mª Dolores Galián Conesa e Francisco Cabello Luque. "Intervención familiar en niños con trastornos del lenguaje: Una revisión." Electronic Journal of Research in Education Psychology 7, n.º 19 (12 de novembro de 2017). http://dx.doi.org/10.25115/ejrep.v7i19.1333.
Texto completo da fonteTeses / dissertações sobre o assunto "Déficits auditifs centraux"
Postal, Olivier. "Déficits centraux auditifs dans les formes génétiques de surdité : l'exemple des gènes Cdhr23 et Pcdh15". Electronic Thesis or Diss., Sorbonne université, 2022. http://www.theses.fr/2022SORUS324.
Texto completo da fonteOver the past three decades, the study of hereditary forms of deafness has provided considerable insight into the molecular mechanisms of hearing, particularly those involved in the development and/or physiology of the auditory sensory organ, the cochlea. In contrast, the genetic approach has provided little information about the central auditory system although many people have central auditory dysfunctions. Central auditory deficits are poorly understood and can, in some cases, go unnoticed. This is likely as a result of cochlear damage depriving the brain of all or part of the acoustic information it would normally receive. To identify genetic forms of deafness that result in both peripheral and central hearing deficits, the Michalski research group uses the susceptibility of mice to audiogenic seizures, epileptic seizures triggered in response to loud sound, which are a manifestation of central deficits. Several strains of mice carrying mutations in deafness genes show susceptibility to audiogenic seizures in the bi-allelic state (if the deafness is not complete) or in the mono-allelic state. Through this strategy, two such genes, Cdhr23 and Pcdh15, have been identified to be involved in the establishment of cortical neurons expressing parvalbumin (PV) which serve as the primary cortical inhibitory neurons in the auditory cortex. The aim of my thesis was a) to develop tools to easily identify the presence of central auditory deficits in genetic models of deafness in mice and b) to further investigate the roles of cdhr23 and pcdh15 in the central auditory system through conditional inactivation of Cdhr23 and Pcdh15 in the mouse brain. First, I developed a non-invasive method to measure auditory cortical evoked potentials in mice and demonstrated that mice respond to certain aversive acoustic features differently to humans for which a large network of neurons (even outside the auditory system) is activated. These results will allow to study more precisely the central deficits associated with hearing impairments. Second, using in vivo electrophysiology and psychoacoustics following the conditional inactivation of Cdhr23 and Pcdh15, I could show that the spectral and temporal characteristics of neuronal responses to sounds were modified without significantly altering their perception by the mice. Furthermore, I was able to better characterise the role of these two genes in the development of PV interneurons. Although a previous study suggested that Cdhr23 and Pcdh15 were expressed in neuroblasts destined to migrate to the auditory cortex, my results show that in fact they are expressed extensively throughout the cortex with the majority in the microglia (for Cdhr23) and in oligodendrocyte progenitors (for Pcdhr15), both populations strongly associated with the development and function of PV interneurons. In addition, Cdhr23 was also found to be expressed in subcortical neuronal populations of the auditory, motor, and multisensory regions. These new advances in demonstrating the role of Cdhr23 and Pcdh15 to be more intricate and indirect than initially thought need to be considered for future investigations into the consequences of their inactivation in the brain. Thus, my results show that two deafness genes have an intrinsic role in the central nervous system without being restricted to auditory circuits and probably participate in many different cellular mechanisms that remain to be explored in order to better characterize the central deficits that might exist in patients carrying CDHR23 or PCDH15 mutations
Castex, Contreras Constanza, Soares Yolanda Castro, Pivet Ximena Sandoval, Rubilar Valentina Seguel e Morales Geraldine Vera. "Rendimiento en Pruebas de Procesamiento Auditivo Central de Adolescentes con y sin Déficit del Discurso Oral". Tesis, Universidad de Chile, 2006. http://www.repositorio.uchile.cl/handle/2250/110663.
Texto completo da fonteCapítulos de livros sobre o assunto "Déficits auditifs centraux"
RODRIGUES, K. C., M. S. NAZARIO, H. P. GODOI, A. E. S. LIMA, I. B. EGÍDIO e N. C. FERNANDES. "DÉFICIT PRECOCE NO DESENVOLVIMENTO COGNITIVO INFANTIL PELO TDAH ASSOCIADO AO TPAC: ESTUDO DE CASO". In TDAH: análises, compreensões e intervenções clínicas e pedagógicas, 57–65. Editora Científica Digital, 2023. http://dx.doi.org/10.37885/221211521.
Texto completo da fonteLima, Victor Silva de, Brenda Rebeca Fernandes de Souza e Ituany da Costa Melo. "A COEXISTÊNCIA DO TRANSTORNO DO PROCESSAMENTO AUDITIVO CENTRAL E O TRANSTORNO DE DÉFICIT DE ATENÇÃO E HIPERATIVIDADE NA INFÂNCIA: REVISÃO BIBLIOGRÁFICA". In TÓPICOS EM FONOAUDIOLOGIA VI: ABORDAGENS EM CIÊNCIAS FONOAUDIOLÓGICAS, 11–29. Editora Inovar, 2023. http://dx.doi.org/10.36926/editorainovar-978-65-5388-179-2_001.
Texto completo da fonteTrabalhos de conferências sobre o assunto "Déficits auditifs centraux"
Santos, Kassia Amanda Viana dos. "TRANSTORNO DO PROCESSAMENTO AUDITIVO CENTRAL E SUAS IMPLICAÇÕES NO DESENVOLVIMENTO DAS HABILIDADES DE LINGUAGEM". In I Congresso Brasileiro On-line de Ensino, Pesquisa e Extensão. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/ensipex/59.
Texto completo da fonte