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• W2163018972 abstract "Hearing developmental dyslexics and profoundly deaf individuals both have difficulties processing the internal structure of words (phonological processing) and learning to read. In hearing non-impaired readers, the development of phonological representations depends on audition. In hearing dyslexics, many argue, auditory processes may be impaired. In congenitally profoundly deaf individuals, auditory speech processing is essentially absent. Two separate literatures have previously reported enhanced activation in the left inferior frontal gyrus in both deaf and dyslexic adults when contrasted with hearing non-dyslexics during reading or phonological tasks. Here, we used a rhyme judgement task to compare adults from these two special populations to a hearing non-dyslexic control group. All groups were matched on non-verbal intelligence quotient, reading age and rhyme performance. Picture stimuli were used since this requires participants to generate their own phonological representations, rather than have them partially provided via text. By testing well-matched groups of participants on the same task, we aimed to establish whether previous literatures reporting differences between individuals with and without phonological processing difficulties have identified the same regions of differential activation in these two distinct populations. The data indicate greater activation in the deaf and dyslexic groups than in the hearing non-dyslexic group across a large portion of the left inferior frontal gyrus. This includes the pars triangularis, extending superiorly into the middle frontal gyrus and posteriorly to include the pars opercularis, and the junction with the ventral precentral gyrus. Within the left inferior frontal gyrus, there was variability between the two groups with phonological processing difficulties. The superior posterior tip of the left pars opercularis, extending into the precentral gyrus, was activated to a greater extent by deaf than dyslexic participants, whereas the superior posterior portion of the pars triangularis extending into the ventral pars opercularis, was activated to a greater extent by dyslexic than deaf participants. Whether these regions play differing roles in compensating for poor phonological processing is not clear. However, we argue that our main finding of greater inferior frontal gyrus activation in both groups with phonological processing difficulties in contrast to controls suggests greater reliance on the articulatory component of speech during phonological processing when auditory processes are absent (deaf group) or impaired (dyslexic group). Thus, the brain appears to develop a similar solution to a processing problem that has different antecedents in these two populations." @default.
• W2163018972 created "2016-06-24" @default.
• W2163018972 creator A5016627829 @default.
• W2163018972 creator A5064018982 @default.
• W2163018972 creator A5070463035 @default.
• W2163018972 creator A5089543470 @default.
• W2163018972 date "2009-05-25" @default.
• W2163018972 modified "2023-10-17" @default.
• W2163018972 title "Enhanced activation of the left inferior frontal gyrus in deaf and dyslexic adults during rhyming" @default.
• W2163018972 cites W1866095408 @default.
• W2163018972 cites W1964870184 @default.
• W2163018972 cites W1976954310 @default.
• W2163018972 cites W1978455957 @default.
• W2163018972 cites W1984330711 @default.
• W2163018972 cites W1985665858 @default.
• W2163018972 cites W1985781047 @default.
• W2163018972 cites W1987334222 @default.
• W2163018972 cites W1989521712 @default.
• W2163018972 cites W1992177291 @default.
• W2163018972 cites W1992258937 @default.
• W2163018972 cites W1997297875 @default.
• W2163018972 cites W1997511158 @default.
• W2163018972 cites W1997846670 @default.
• W2163018972 cites W2001899083 @default.
• W2163018972 cites W2001930671 @default.
• W2163018972 cites W2001933204 @default.
• W2163018972 cites W2010266978 @default.
• W2163018972 cites W2014765835 @default.
• W2163018972 cites W2016587151 @default.
• W2163018972 cites W2017971431 @default.
• W2163018972 cites W2019172679 @default.
• W2163018972 cites W2022302764 @default.
• W2163018972 cites W2024449923 @default.
• W2163018972 cites W2025872140 @default.
• W2163018972 cites W2026732271 @default.
• W2163018972 cites W2034717889 @default.
• W2163018972 cites W2035843433 @default.
• W2163018972 cites W2036975455 @default.
• W2163018972 cites W2039153215 @default.
• W2163018972 cites W2043423994 @default.
• W2163018972 cites W2049582292 @default.
• W2163018972 cites W2054032682 @default.
• W2163018972 cites W2055972389 @default.
• W2163018972 cites W2056032818 @default.
• W2163018972 cites W2056306065 @default.
• W2163018972 cites W2060985254 @default.
• W2163018972 cites W2064563223 @default.
• W2163018972 cites W2066228684 @default.
• W2163018972 cites W2068390239 @default.
• W2163018972 cites W2077810023 @default.
• W2163018972 cites W2081162205 @default.
• W2163018972 cites W2082244577 @default.
• W2163018972 cites W2082493063 @default.
• W2163018972 cites W2084079188 @default.
• W2163018972 cites W2089960403 @default.
• W2163018972 cites W2090655720 @default.
• W2163018972 cites W2092964121 @default.
• W2163018972 cites W2094908156 @default.
• W2163018972 cites W2095182071 @default.
• W2163018972 cites W2100128223 @default.
• W2163018972 cites W2100697074 @default.
• W2163018972 cites W2107627409 @default.
• W2163018972 cites W2113093303 @default.
• W2163018972 cites W2113337499 @default.
• W2163018972 cites W2114112991 @default.
• W2163018972 cites W2116317598 @default.
• W2163018972 cites W2116842140 @default.
• W2163018972 cites W2120203426 @default.
• W2163018972 cites W2121540313 @default.
• W2163018972 cites W2122974659 @default.
• W2163018972 cites W2124481262 @default.
• W2163018972 cites W2126771874 @default.
• W2163018972 cites W2128388643 @default.
• W2163018972 cites W2128672892 @default.
• W2163018972 cites W2130776005 @default.
• W2163018972 cites W2131785404 @default.
• W2163018972 cites W2134058067 @default.
• W2163018972 cites W2137475052 @default.
• W2163018972 cites W2139610547 @default.
• W2163018972 cites W2142869478 @default.
• W2163018972 cites W2144157660 @default.
• W2163018972 cites W2144218267 @default.
• W2163018972 cites W2146991114 @default.
• W2163018972 cites W2147768668 @default.
• W2163018972 cites W2154059262 @default.
• W2163018972 cites W2157864874 @default.
• W2163018972 cites W2157915068 @default.
• W2163018972 cites W2160244607 @default.
• W2163018972 cites W2161873289 @default.
• W2163018972 cites W2168101244 @default.
• W2163018972 cites W2168423440 @default.
• W2163018972 cites W2170514299 @default.
• W2163018972 cites W2171652727 @default.
• W2163018972 cites W2226027519 @default.
• W2163018972 cites W4256047805 @default.
• W2163018972 cites W4293107615 @default.
• W2163018972 doi "https://doi.org/10.1093/brain/awp129" @default.
• W2163018972 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2702837" @default.

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