Results 151 to 160 of about 500,614 (355)
Ataxic speech disorders and Parkinson's disease diagnostics via stochastic embedding of empirical mode decomposition. [PDF]
Campi M, Peters GW, Toczydlowska D.
europepmc +1 more source
Compromised Speech Processing in Language Disorders [PDF]
The relationship between the control of processes required for speech and language production were investigated in the context of fluency analysis of natural language samples produced by aphasic speakers.
Hird, Kathryn, Kirsner, Kim
core +1 more source
Real‐World Performance of CSF Kappa Free Light Chains in the 2024 McDonald Criteria
ABSTRACT Objective Kappa free light chains (KFLCs) in the cerebrospinal fluid (CSF) have a similar performance to CSF‐restricted oligoclonal bands (OCB) for multiple sclerosis (MS) diagnosis. To help with implementation, we set out to resolve several remaining uncertainties: (1) performance in a real‐world cohort and the 2024 McDonald criteria; (2 ...
Maya M. Leibowitz +11 more
wiley +1 more source
Communication and Social Interaction Experiences of Youths With Congenital Motor Speech Disorders. [PDF]
Connaghan KP +4 more
europepmc +1 more source
Diagnostic Utility of the ATG9A Ratio in AP‐4–Associated Hereditary Spastic Paraplegia
ABSTRACT Adaptor protein complex 4–associated hereditary spastic paraplegia (AP‐4‐HSP), a childhood‐onset neurogenetic disorder and frequent mimic of cerebral palsy, is caused by biallelic variants in the adaptor protein complex 4 (AP‐4) subunit genes (AP4B1 [for SPG47], AP4M1 [for SPG50], AP4E1 [for SPG51], and AP4S1 [for SPG52]).
Habibah A. P. Agianda +12 more
wiley +1 more source
Purpose This study aims to examine the association of tinnitus acceptance on sleep quality and depression in chronic tinnitus patients, addressing a gap in the literature on acceptance processes and quality of life.
Sevgi Kutlu +3 more
doaj +1 more source
A Brain Marker for Developmental Speech Disorders
Angela Morgan +5 more
openalex +2 more sources
Clinically Relevant Outcome Measures in Women With Adrenoleukodystrophy
ABSTRACT Adrenoleukodystrophy is a rare inherited peroxisomal disease caused by pathogenic variants in the ABCD1 gene located on the X chromosome. Although the most severe central nervous system and adrenal complications typically affect only men with adrenoleukodystrophy, the majority of women develop myeloneuropathy symptoms in adulthood.
Chenwei Yan +3 more
wiley +1 more source
Perceptual benefits from digital noise reduction (NR) vary among individuals with different noise tolerance and sensitivity to distortions introduced in NR-processed speech; however, the physiological bases of the variance are understudied.
Subong Kim +2 more
doaj +1 more source
Speech disorders in patients with Tongue squamous cell carcinoma: A longitudinal observational study based on a questionnaire and acoustic analysis. [PDF]
Guo K +7 more
europepmc +1 more source

