Results 31 to 40 of about 1,015 (189)

Apraxia e produção da fala: efeitos do fortalecimento de relações verbais

open access: yesRevista CEFAC, 2015
Este estudo propõe relatar o efeito do fortalecimento de relações de leitura e da transferência de controle de estímulos sobre a produção da fala de uma criança com apraxia de fala.
Ana Claudia Moreira Almeida-Verdu   +6 more
doaj   +1 more source

Patient and Family Reported Clinical Picture of IRF2BPL‐Related Disorders

open access: yesAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT IRF2BPL‐related disorder is a neurodevelopmental disorder caused by heterozygous variants in the IRF2BPL (Interferon Regulatory Factor 2 Binding Protein‐Like) gene. The few reports available in the literature suggest that common symptoms include developmental delay, intellectual disability, and developmental regression.
Zoe Goldstone‐Joubert   +4 more
wiley   +1 more source

Avaliação de apraxias em pacientes com lesão cerebrovascular em hemisfério esquerdo

open access: yesPsicologia, 2011
Los estudios muestran la dominancia del hemisferio cerebral izquierdo (HI) en la planificación motora, pero se necesitan más investigaciones sobre la participación de las regiones corticales y subcorticales del HI en las apraxias.
Jaqueline de Carvalho Rodrigues   +4 more
doaj  

Diferencias práxicas según subtipos de deterioro cognitivo en un grupo de pacientes con enfermedad de Parkinson avanzada

open access: yesMedicina U.P.B., 2019
Objetivo: se habla de enfermedad de Parkinson (EP) avanzada cuando la terapia convencional no proporciona control motor. Las alteraciones práxicas se han descrito en estos pacientes, como parte del deterioro cognitivo leve (DCL) desde etapas tempranas ...
David Andrés Montoya-Arenas   +3 more
doaj   +1 more source

Severity and Co-occurrence of Oral and Verbal Apraxias in Left Brain Damaged Adults

open access: yesJournal of Rehabilitation, 2012
Objective: Oral and verbal apraxias represent motor programming deficits of nonverbal and verbal movements respectively. Studying their properties may shed light on speech motor control processes.
Fariba Yadegari   +3 more
doaj  

Exocrine Gland Dysfunction in Parkinson's Disease: Pathophysiology, Clinical Manifestations, and Therapeutic Perspectives—A Narrative Review

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background Non‐motor symptoms, especially autonomic dysfunction, are major contributors to disability and decreased quality of life in Parkinson's disease (PD). Despite being common and having a wide range of clinical facets, exocrine gland dysfunction is still not well recognized and managed.
Renato P. Munhoz   +2 more
wiley   +1 more source

Cortical Lewy Body Dementia

open access: yesBehavioural Neurology, 1990
In cortical Lewy body dementia the distribution of Lewy bodies in the nervous system follows that of Parkinson's disease, except for their greater profusion in the cerebral cortex. The cortical tangles and plaques of Alzheimer pathology are often present,
W. R. G. Gibb
doaj   +1 more source

Relapsing Depression in Paramedian Thalamic Infarctions

open access: yesBehavioural Neurology, 1992
Depression has recently been associated with lesions in the CNS, particularly with large infarctions in the cerebral hemispheres. We report a patient in whom two episodes of acute depression were related to relapsing paramedian thalamic infarctions ...
R. W. Baumgartner, T. Landis, M. Regard
doaj   +1 more source

Apraxia de fala na infância: análise da percepção e conduta dos fonoaudiólogos sobre o processo de avaliação [PDF]

open access: yesAudiology: Communication Research
RESUMO Objetivo analisar a percepção e conduta dos fonoaudiólogos sobre o processo de avaliação no diagnóstico diferencial de apraxia de fala na infância.
João Manoel Ferro Castro   +2 more
doaj   +4 more sources

Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case‐Series and Literature Review

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Sangeetha Yoganathan   +14 more
wiley   +1 more source

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