Results 41 to 50 of about 14,238 (236)

Prevalence of risk factors for stuttering among boys: analytical cross-sectional study

open access: yesSão Paulo Medical Journal
CONTEXT AND OBJECTIVE:There have been few studies on the risk factors for subgroups of stuttering. The aim of this study was to characterize the risk factors for developmental familial stuttering among boys who stutter and who do not stutter, such as ...
Cristiane Moço Canhetti Oliveira   +1 more
doaj   +1 more source

Testosterone level of children with the diagnosis of developmental stuttering

open access: yesPsychiatry and Clinical Psychopharmacology, 2021
Objective: The effect of gender in development and chronicity of stuttering is well known. It is more common and chronic in males. In this study, it is aimed to investigate the relation between developmental stuttering and the serum level of ...
Engin Burak Selcuk   +4 more
doaj  

Subtypes of stuttering determined by latent class analysis in two Swiss epidemiological surveys. [PDF]

open access: yesPLoS ONE, 2018
AIMS:Associations between stuttering in childhood and a broad spectrum of risk factors, associated factors and comorbidities were examined in two large epidemiological studies.
Vladeta Ajdacic-Gross   +13 more
doaj   +1 more source

Altered Auditory Feedback In-The-Ear Devices [PDF]

open access: yes, 2004
Purpose: This study examined objective and subjective measures of the effect of a self-contained ear-level device delivering altered auditory feedback (AAF) for those who stutter 12 months following initial fitting with and without the device.
American National Standards Institute   +16 more
core   +1 more source

The neurological underpinnings of cluttering: Some initial findings [PDF]

open access: yes, 2015
Background Cluttering is a fluency disorder characterised by overly rapid or jerky speech patterns that compromise intelligibility. The neural correlates of cluttering are unknown but theoretical accounts implicate the basal ganglia and medial ...
Bretherton-Furness, Jess   +4 more
core   +1 more source

The Link Between Syntactic Complexity and Stuttering-Like Disfluencies in French Speaking Adults. [PDF]

open access: yesInt J Lang Commun Disord
ABSTRACT Background Stuttering is a neurodevelopmental disorder characterized by speech disfluencies. While studies have shown a link between syntactic complexity and stuttering in children, its role in adults who stutter (AWS) remains unclear. This study investigates whether increased syntactic complexity correlates with stuttering‐like disfluencies ...
Dévic AL, Diwersy S, Didirková I.
europepmc   +2 more sources

ResearchConnect: An AI‐Powered Platform for Interdisciplinary Research Team Formation and Ideation Development

open access: yesAdvanced Intelligent Systems, EarlyView.
ResearchConnect is an AI‐powered platform that automates researcher profiling, interdisciplinary team formation, and early‐stage research ideation. By extracting keywords from papers and web sources, it quickly clusters researchers into coherent teams and generates collaborative ideas using large language models. Validation on NSF‐funded projects shows
Akshay Vilas Jadhav   +2 more
wiley   +1 more source

Compilation of a preliminary checklist for the differential diagnosis of neurogenic stuttering

open access: yesSouth African Journal of Communication Disorders, 2014
Background: Neurogenic stuttering (NS) is the most frequently occurring acquired form of stuttering in children and adults. This form of stuttering is primarily caused by neurological incidents.
Mariska Lundie   +3 more
doaj   +1 more source

Acoustically controlled auditory training in children with speech disfluency: a case report

open access: yesRevista CEFAC, 2020
The purpose of this study was to verify the effect of the acoustically controlled auditory training on the speech fluency of children diagnosed with developmental stuttering.
Priscila Biaggi Alves de Alencar   +5 more
doaj   +2 more sources

Marfan Syndrome Associated With Intellectual Disability and Behavioral Anomalies: Further Evidence for the Effect of Compound Heterozygous Variants in FBN1 on Phenotypic Severity

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Marfan syndrome (MFS) is a rare connective tissue disorder characterized by involvement of the cardiovascular, ocular, and musculoskeletal systems. Pathogenic variants in FBN1 cause most of the MFS cases; however, intellectual disability (ID) is rarely observed. A non‐consanguineous Pakistani family with four affected individuals was recruited.
Azmatullah Khan   +4 more
wiley   +1 more source

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