ライフサイエンスコーパス: neurotypical

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1 c gene expression in multiple data sets from neurotypical adult and prenatal human neocortical tissue

2 Sixty right-handed neurotypical adult men aged 18 to 45 years, and 60 right

3 ltered brain function in reward circuitry in neurotypical adults and may increase risk for autism spe

4 that adults with ASD are less surprised than neurotypical adults when their expectations are violated

5 We showed that, like infants, neurotypical adults' (n = 17 participants) eye movements

6 ultivoxel pattern analysis, find that (i) in neurotypical adults, the RTPJ shows reliable and distinc

7 esonance imaging scans were collected for 25 neurotypical adults.

8 al network was related to autistic traits in neurotypical adults.

9 naptic genes in postmortem cerebella from 14 neurotypical and 11 autistic individuals.

10 Whereas neurotypical brain activity frequently transits between

11 hanisms by which maternal UBE3A loss derails neurotypical brain growth and function.

12 h, compared to a control group of parents of neurotypical children (N = 20), as well as to nonaloof p

13 Using data from 41 children with ASD and 41 neurotypical children, we examined functional connectivi

14 as demonstrated in autistic children than in neurotypical children.

15 h-functioning adults with ASD and 98 matched neurotypical control individuals aged 18 to 42 years.

16 of 14 individuals with AS and a group of 14 neurotypical control participants performed a face-match

17 Compared with neurotypical control participants, participants with ASD

18 h included unaffected siblings and unrelated neurotypical controls (ages 3-12 y; n = 193), whether pl

19 d with areas that were sexually dimorphic in neurotypical controls, in both grey and white matter, su

20 left hemisphere activations for language in neurotypical controls, participants with complete or par

21 t males with autism spectrum disorder and 61 neurotypical controls, using two complementary approache

22 stem connectivity in both youth with ASD and neurotypical controls.

23 ts with autism spectrum disorder relative to neurotypical controls.

24 with ASC showed similar deficits compared to neurotypical controls.

25 s assessed via magnetic resonance imaging in neurotypical controls.

26 als with high-functioning ASDs compared with neurotypical, demographically matched controls.

27 es, females with ASC performed comparably to neurotypical females.

28 Here neuromodulation of RCrusI in neurotypical humans resulted in altered functional conne

29 howed "shallower" sigmoid curves compared to neurotypicals, indicating the presence of an indistinct

30 Neurotypical individuals often experience a subjective r

31 Neurotypical individuals preferentially recruit the midd

32 ned the neural correlates of these traits in neurotypical individuals using the SRS-A and established

33 of the corpus callosum (AgCC) and 21 matched neurotypical individuals.

34 sm spectrum condition and age and IQ-matched neurotypical males while they made reflective mentalizin

35 th ASC showed poorer performance relative to neurotypical males, females with ASC performed comparabl

36 Results showed that, similar to neurotypical (NT) adults, ASD adults were faster to reco

37 In experiment 1, ASD and neurotypical (NT) participants performed a ToM task desi

38 r neurotypical which results in 96.1% of all neurotypical participants being correctly identified as

39 Here, 38 neurotypical participants underwent two fMRI sessions ac

40 gments based less on intent information than neurotypical participants.

41 ith MLD are significantly discriminable from neurotypical peers before, but not after, tutoring, sugg

42 83 participants with ASD and 76 age-matched neurotypical peers.

43 in individuals with ASD as prerequisites for neurotypical social interaction.

44 on of the participants as on the spectrum or neurotypical which results in 96.1% of all neurotypical

45 -allele dosage and symptom severity, whereas neurotypical youth showed increased NAcc connectivity wi

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