Δευτέρα 27 Φεβρουαρίου 2017

Indexing cortical entrainment to natural speech at the phonemic level: Methodological considerations for applied research

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Publication date: Available online 27 February 2017
Source:Hearing Research
Author(s): Giovanni M. Di Liberto, Edmund C. Lalor
Speech is central to human life. As such, any delay or impairment in receptive speech processing can have a profoundly negative impact on the social and professional life of a person. Thus, being able to assess the integrity of speech processing in different populations is an important goal. Current standardized assessment is mostly based on psychometric measures that do not capture the full extent of a person’s speech processing abilities and that are difficult to administer in some subjects groups. A potential alternative to these tests would be to derive “direct”, objective measures of speech processing from cortical activity. One such approach was recently introduced and showed that it is possible to use electroencephalography (EEG) to index cortical processing at the level of phonemes from responses to continuous natural speech. However, a large amount of data was required for such analyses. This limits the usefulness of this approach for assessing speech processing in particular cohorts for whom data collection is difficult. Here, we used EEG data from 10 subjects to assess whether measures reflecting phoneme-level processing could be reliably obtained using only 10 minutes of recording time from each subject. This was done successfully using a generic modeling approach wherein the data from a training group composed of 9 subjects were combined to derive robust predictions of the EEG signal for new subjects. This allowed the derivation of indices of cortical activity at the level of phonemes and the disambiguation of responses to specific phonetic features (e.g., stop, plosive, and nasal consonants) with limited data. This objective approach has the potential to complement psychometric measures of speech processing in a wide variety of subjects.



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Antibiotics used to treat cystic fibrosis increases risk of permanent hearing loss

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Antibiotics used to treat cystic fibrosis increases risk of permanent hearing loss

A powerful class of antibiotics provides life-saving relief for people with cystic fibrosis; however, a new study for the first time reveals the levels at which high cumulative dosages over time...

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Antibiotics used to treat cystic fibrosis increases risk of permanent hearing loss

A powerful class of antibiotics provides life-saving relief for people with cystic fibrosis; however, a new study for the first time reveals the levels at which high cumulative dosages over time...

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Familial hematuria: A review.

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Authors: Plevová P, Gut J, Janda J

Abstract
The most frequent cause of familial glomerular hematuria is thin basement membrane nephropathy (TBMN) caused by germline COL4A3 or COL4A4 gene mutations. Less frequent but important cause with respect to morbidity is Alport syndrome caused by germline COL4A5 gene mutations. The features of Alport syndrome include hematuria, proteinuria and all males with X-linked disease and all individuals with recessive disease will develop end stage renal disease, usually at early youth. In X-linked Alport syndrome, a clear genotype-phenotype correlation is typically observed in men. Deleterious COL4A5 mutations are associated with a more severe renal phenotype and more frequent high-frequency sensorineural hearing loss and ocular abnormalities. Less severe COL4A5 mutations result in a milder phenotype, with less frequent and later onset extrarenal anomalies. The phenotype in females is highly variable, mostly due to inactivation of one of the X chromosomes. Isolated cases may be caused by de novo COL4A5 mutations or by gonosomal mosaicism. Untreated autosomal recessive Alport syndrome, caused by COL4A3 and COL4A4 mutations, is typically associated with ESRD at the age of 23-25 years and extrarenal symptoms in both men and women. The TBMN phenotype is associated with heterozygous carriers of COL4A3, COL4A4 mutations. Molecular genetic testing is the gold standard for diagnosing these diseases. Although genotype-phenotype correlations exist, the phenotype is influenced by modifying factors, which remain mainly undefined. No therapy is available that targets the cause of Alport syndrome; angiotensin-converting enzyme inhibitor therapy delays renal failure and improves lifespan.

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Audiologists’ communication behaviour during hearing device management appointments

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The accuracy of objective threshold determination at low frequencies: comparison of different auditory brainstem response (ABR) and auditory steady state response (ASSR) methods

.


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Book Review

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Audiologists’ communication behaviour during hearing device management appointments

.


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The accuracy of objective threshold determination at low frequencies: comparison of different auditory brainstem response (ABR) and auditory steady state response (ASSR) methods

.


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Book Review

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Abstract
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Vestibular stimulation improves insight into illness in schizophrenia spectrum disorders.

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Psychiatry Res. 2017 Feb 13;251:333-341

Authors: Gerretsen P, Pothier DD, Falls C, Armstrong M, Balakumar T, Uchida H, Mamo DC, Pollock BG, Graff-Guerrero A

Abstract
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PMID: 28237912 [PubMed - as supplied by publisher]



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