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Relevant bibliographies by topics / Orofacial apraxia

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Journal articles

Academic literature on the topic 'Orofacial apraxia'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Orofacial apraxia"

1

Cera, Maysa Luchesi, Karin Zazo Ortiz, Paulo Henrique Ferreira Bertolucci, and Thaís Soares Cianciarullo Minett. "Speech and orofacial apraxias in Alzheimer's disease." International Psychogeriatrics 25, no. 10 (2013): 1679–85. http://dx.doi.org/10.1017/s1041610213000781.

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ABSTRACTBackground:Alzheimer's disease (AD) affects not only memory but also other cognitive functions, such as orientation, language, praxis, attention, visual perception, or executive function. Most studies on oral communication in AD focus on aphasia; however, speech and orofacial apraxias are also present in these patients. The aim of this study was to investigate the presence of speech and orofacial apraxias in patients with AD with the hypothesis that apraxia severity is strongly correlated with disease severity.Methods:Ninety participants in different stages of AD (mild, moderate, and s

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2

Roth, Heidi L., Thomas A. Eskin, Diane L. Kendall, and Kenneth M. Heilman. "Progressive Oculo-Orofacial-Speech Apraxia (POOSA)." Neurocase 12, no. 4 (2006): 221–27. http://dx.doi.org/10.1080/13554790600837347.

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Pita Lobo, Patrícia, Susana Pinto, Luz Rocha, Sofia Reimão, and Mamede de Carvalho. "Orofacial Apraxia in Motor Neuron Disease." Case Reports in Neurology 5, no. 1 (2013): 47–51. http://dx.doi.org/10.1159/000349895.

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4

Cera, Maysa, Karin Ortiz, Paulo Bertolucci, and Thais Minett. "P1-399: Apraxia of speech and orofacial apraxia in Alzheimer's disease." Alzheimer's & Dementia 7 (July 2011): S240. http://dx.doi.org/10.1016/j.jalz.2011.05.680.

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5

Gubiani, Marileda Barichello, Karina Carlesso Pagliarin, and Marcia Keske-Soares. "Instrumentos para avaliação de apraxia de fala infantil." CoDAS 27, no. 6 (2015): 610–15. http://dx.doi.org/10.1590/2317-1782/20152014152.

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RESUMO Objetivo: Revisar sistematicamente na literatura os principais instrumentos utilizados para avaliação da apraxia de fala infantil. Estratégia de pesquisa: Realizou-se busca nas bases Scopus, PubMed e Embase Critérios de seleção: Foram selecionados estudos empíricos que utilizaram instrumentos de avaliação da apraxia de fala infantil. Análise dos dados: A seleção dos artigos foi realizada por dois pesquisadores independentes. Resultados: Foram encontrados 695 resumos. Após a leitura dos resumos, foram selecionados 12 artigos completos. Foi possível identificar cinco instrumentos: Verbal

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6

�zsancak, Canan, Pascal Auzou, and Didier Hannequin. "Dysarthria and orofacial apraxia in corticobasal degeneration." Movement Disorders 15, no. 5 (2000): 905–10. http://dx.doi.org/10.1002/1531-8257(200009)15:5<905::aid-mds1022>3.0.co;2-d.

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7

McNeil, Malcolm R., Gary Weismer, Scott Adams, and Moira Mulligan. "Oral Structure Nonspeech Motor Control in Normal, Dysarthric, Aphasic and Apraxic Speakers." Journal of Speech, Language, and Hearing Research 33, no. 2 (1990): 255–68. http://dx.doi.org/10.1044/jshr.3302.255.

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This study investigated the isometric force and static position control of the upper lip, lower lip, tongue, jaw, and finger in four subject groups (normal control, apraxia of speech, conduction aphasia, and ataxic dysarthria) at two force and displacement levels. Results from both the force and position tasks suggested that the apraxic and dysarthric groups tended to produce significantly greater instability than the normal group, although the pattern of instability across articulators was not systematic within or across the force and position experiments for subjects within or between groups

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8

Bhardwaj, Parveen, Minoo Sharma, and Karan Ahluwalia. "Joubert Syndrome with Orofacial Digital Features." Journal of Neurosciences in Rural Practice 09, no. 01 (2018): 152–54. http://dx.doi.org/10.4103/jnrp.jnrp_338_17.

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ABSTRACTJoubert syndrome (JS) is an autosomal recessive inherited disorder characterized by hypotonia, cerebellar vermis hypoplasia, ocular abnormalities (e.g., pigmentary retinopathy, oculomotor apraxia, and nystagmus), renal cysts, and hepatic fibrosis. Respiratory abnormalities, as apnea and hyperpnea, may be present, as well as mental retardation. Since the clinical findings of JS are quite heterogeneous, determination of radiological findings is essential.

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9

Tomaiuolo, Francesco, Serena Campana, Loredana Voci, Stefano Lasaponara, Fabrizio Doricchi, and Michael Petrides. "The Precentral Insular Cortical Network for Speech Articulation." Cerebral Cortex 31, no. 8 (2021): 3723–31. http://dx.doi.org/10.1093/cercor/bhab043.

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Abstract Apraxia of speech is a motor disorder characterized by the impaired ability to coordinate the sequential articulatory movements necessary to produce speech. The critical cortical area(s) involved in speech apraxia remain controversial because many of the previously reported cases had additional aphasic impairments, preventing localization of the specific cortical circuit necessary for the somatomotor execution of speech. Four patients with “pure speech apraxia” (i.e., who had no aphasic and orofacial motor impairments) are reported here. The critical lesion in all four patients involv

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10

Ray, Jayanti. "Effects of orofacial myofunctional therapy on speech intelligibility in individuals with persistent articulatory impairments." International Journal of Orofacial Myology 29, no. 1 (2003): 5–14. http://dx.doi.org/10.52010/ijom.2003.29.1.1.

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This study examined the effects of orofacial myofunctional therapy (OMT) on speech intelligibility in adults with persistent articulation impairments. Six adults in the age range of 18-23 years were selected to receive orofacial myofunctional therapy for a period of six weeks. The results showed that five out of six clients made significant progress in oral postures and speech sound production across all three speech production tasks: single words, sentences, and spontaneous speech. Speech intelligibility increased significantly in all clients except the one diagnosed with developmental apraxi

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