Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Irene Hidalgo de La Guía"'
Publikováno v:
Revista de Investigación en Logopedia, Vol 9, Iss 2 (2019)
Los trastornos del neurodesarrollo presentes en alteraciones como el síndrome de Down, el síndrome de Williams y el síndrome de Smith Magenis subyacen en las características cognitivas, conductuales y lingüísticas de quienes los padecen. Pese a
Externí odkaz:
https://doaj.org/article/6e2be2ff9bae41f19e6f12785cd467fc
Autor:
Irene Hidalgo-De la Guía, Elena Garayzábal-Heinze, Pedro Gómez-Vilda, Rafael Martínez-Olalla, Daniel Palacios-Alonso
Publikováno v:
Frontiers in Human Neuroscience, Vol 15 (2021)
Complex simultaneous neuropsychophysiological mechanisms are responsible for the processing of the information to be transmitted and for the neuromotor planning of the articulatory organs involved in speech. The nature of this set of mechanisms is cl
Externí odkaz:
https://doaj.org/article/96767713a17e4229b34c8d855b132fdf
Autor:
Carlos Romero-Rivas, Sara Rodríguez-Cuadrado, Lucía Sabater, Pablo Rodríguez Gómez, Irene Hidalgo de la Guía, Eva M. Moreno, Elena Garayzábal Heinze
Publikováno v:
Language and Cognition. :1-25
Williams syndrome (WS) is a rare genetic disorder, characterised at the cognitive level by a phenotypic pattern of relative weaknesses (e.g., visuospatial skills) and strengths (e.g., some linguistic and nonverbal reasoning skills). In this study, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2bebde40bd79b2aacb6cf2bb04720bb
https://doi.org/10.1017/langcog.2023.15
https://doi.org/10.1017/langcog.2023.15
Autor:
Kriscia Gobi Rosa, Célia Maria Giacheti, Natalia Freitas Rossi, Elena Garayzábal Heinze, Irene Hidalgo de la Guía
Publikováno v:
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2021-06-25T10:56:45Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-01-01 Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Smith–Magenis syndrome (SMS) is a rare neurodevelopmental disorder w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a09c782eb1c2a28f7de02ef242cf0f93
https://doi.org/10.1016/j.rlfa.2020.09.006
https://doi.org/10.1016/j.rlfa.2020.09.006
Autor:
Elena Garayzábal-Heinze, Pedro Gómez-Vilda, Irene Hidalgo de la Guía, Daniel Palacios-Alonso, Rafael Martínez-Olalla
Publikováno v:
Frontiers in Human Neuroscience, Vol 15 (2021)
Frontiers in Human Neuroscience
Frontiers in Human Neuroscience
Complex simultaneous neuropsychophysiological mechanisms are responsible for the processing of the information to be transmitted and for the neuromotor planning of the articulatory organs involved in speech. The nature of this set of mechanisms is cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca392e693381aab46be6137d8705f8d6
https://doi.org/10.3389/fnhum.2021.661392
https://doi.org/10.3389/fnhum.2021.661392
Publikováno v:
Languages
Volume 5
Issue 3
Languages, Vol 5, Iss 31, p 31 (2020)
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Volume 5
Issue 3
Languages, Vol 5, Iss 31, p 31 (2020)
Biblos-e Archivo. Repositorio Institucional de la UAM
instname
Smith&ndash
Magenis syndrome (SMS) is a rare genetic disease characterized by intellectual disability, serious behavior disorders, neurodevelopment delay, and speech and language disorders. An acoustic and biomechanical analysis of the voice of
Magenis syndrome (SMS) is a rare genetic disease characterized by intellectual disability, serious behavior disorders, neurodevelopment delay, and speech and language disorders. An acoustic and biomechanical analysis of the voice of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ea79fcc68155f4e35a2fa97bc0d3d8e
Publikováno v:
Avaliação da fala e da linguagem: perspectivas interdisciplinares em Fonoaudiologia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::867847a2b826b4dd29cbd9c2c59bb8c4
https://doi.org/10.36311/2020.978-65-86546-87-3.p29-48
https://doi.org/10.36311/2020.978-65-86546-87-3.p29-48
Publikováno v:
Avaliação da fala e da linguagem: perspectivas interdisciplinares em Fonoaudiologia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a82fe185ccaf1cf10ca7d942047e4133
https://doi.org/10.36311/2020.978-65-86546-87-3.p397-406
https://doi.org/10.36311/2020.978-65-86546-87-3.p397-406
Publikováno v:
Biblos-e Archivo: Repositorio Institucional de la UAM
Universidad Autónoma de Madrid
Revista de Investigación en Logopedia, Vol 9, Iss 2, Pp 81-106 (2019)
Biblos-e Archivo. Repositorio Institucional de la UAM
Consejo Superior de Investigaciones Científicas (CSIC)
Universidad Autónoma de Madrid
Revista de Investigación en Logopedia, Vol 9, Iss 2, Pp 81-106 (2019)
Biblos-e Archivo. Repositorio Institucional de la UAM
Consejo Superior de Investigaciones Científicas (CSIC)
Los trastornos del neurodesarrollo presentes en alteraciones como el síndrome de Down, el síndrome de Williams y el síndrome de Smith Magenis subyacen en las características cognitivas, con - ductuales y lingüísticas de quienes los padecen. Pes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc7be864beffc34a3f5f9fe28544f219
https://hdl.handle.net/10486/691822
https://hdl.handle.net/10486/691822
Publikováno v:
Biomedical Signal Processing and Control. 63:102219
Down Syndrome (DS) has been the aim of numerous studies, although its phonation specificities have not received much attention. DS is a genetic disorder caused by the presence of a third copy of chromosome 21, being the explanation of different behav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d4e79e300c6d8a2638ac0e92ab20176
https://doi.org/10.1016/j.bspc.2020.102219
https://doi.org/10.1016/j.bspc.2020.102219