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Journal of Neurodevelopmental Disorders
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1. Quantitative gait assessment in children with 16p11.2 syndrome
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Sylvie Goldman, Aston K. McCullough.
2. Vocabulary comprehension in adults with fragile X syndrome (FXS)
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Anne Hoffmann, Sue Ellen Krause, Joanne Wuu.
3. Behavioural and psychological characteristics in Pitt-Hopkins syndrome: a comparison with Angelman and Cornelia de Lange syndromes
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Alice Watkins, Stacey Bissell, Jo Moss.
4. Developmental divergence: motor trajectories in children with fragile X syndrome with and without co-occurring autism
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Elizabeth A. Will, Somer L. Bishop.
5. Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism
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Carla A. Wall, Abigail L. Hogan.
6. Within-task variability on standardized language tests predicts autism spectrum disorder: a pilot study of the Response Dispersion Index
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Abby E. Hare-Harris, Marissa W. Mitchel.
7. Assessing general cognitive and adaptive abilities in adults with Down syndrome: a systematic review
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Sarah Hamburg, Bryony Lowe, Carla Marie Startin.
8. Magnetoencephalographic (MEG) brain activity during a mental flexibility task suggests some shared neurobiology in children with neurodevelopmental disorders
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Alexandra Mogadam, Anne E. Keller.
9. Phenotypic characterization of individuals with SYNGAP1 pathogenic variants reveals a potential correlation between posterior dominant rhythm and developmental progression
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Andres Jimenez-Gomez, Sizhe Niu.
10. STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics
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Sinéad O’Brien, Elise Ng-Cordell.
11. A phase 1/2, open-label assessment of the safety, tolerability, and efficacy of transdermal cannabidiol (ZYN002) for the treatment of pediatric fragile X syndrome
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Helen Heussler, Jonathan Cohen, Natalie Silove.
12. Electroencephalographic spectral power as a marker of cortical function and disease severity in girls with Rett syndrome
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Katherine J. Roche, Jocelyn J. LeBlanc.
13. Infant regulatory function acts as a protective factor for later traits of autism spectrum disorder and attention deficit/hyperactivity disorder but not callous unemotional traits
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Rachael Bedford, Teodora Gliga, Alexandra Hendry.
14. A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case
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Claudia Ismania Samogy-Costa.
15. Children with facial paralysis due to Moebius syndrome exhibit reduced autonomic modulation during emotion processing
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Elisa De Stefani, Martina Ardizzi.
16. Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders
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Joanne Trinh, Krishna Kumar Kandaswamy.
17. Impaired neurodevelopmental pathways in autism spectrum disorder: a review of signaling mechanisms and crosstalk
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Santosh Kumar, Kurt Reynolds, Yu Ji, Ran Gu.
18. Lesser suppression of response to bright visual stimuli and visual abnormality in children with autism spectrum disorder: a magnetoencephalographic study
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Sho Aoki, Kuriko Kagitani-Shimono.
19. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome
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Adam C. Cunningham, Liam Hill, Mark Mon-Williams.
20. In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
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Zahra Motahari, Sally Ann Moody.
21. Lifespan trajectory of affect in Cornelia de Lange syndrome: towards a neurobiological hypothesis
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Laura Groves, Joanna Moss, Hayley Crawford.
22. Adaptation to different communicative contexts: an eye tracking study of autistic adults
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Julia Parish-Morris, Ashley A. Pallathra.
23. Cognitive training for children and adolescents with fragile X syndrome: a randomized controlled trial of Cogmed
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David Hessl, Julie B. Schweitzer, Danh V. Nguyen.
24. Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
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Gregory Costain, Susan Walker, Bob Argiropoulos.
25. Static and dynamic postural control deficits in aging fragile X mental retardation 1 (FMR1) gene premutation carriers
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Zheng Wang, Pravin Khemani, Lauren M. Schmitt.
26. Differentiating social preference and social anxiety phenotypes in fragile X syndrome using an eye gaze analysis: a pilot study
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Michael P. Hong, Eleanor M. Eckert.
27. Initial eye gaze to faces and its functional consequence on face identification abilities in autism spectrum disorder
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Kimberly B. Schauder, Woon Ju Park, Yuliy Tsank.
28. Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
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Emma K. Baker, Marta Arpone, Solange Aliaga Vera.
29. Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome
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Kathryn L. McCabe, Abbie M. Popa.
30. Adaptation of the Clinical Dementia Rating Scale for adults with Down syndrome
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Christina N. Lessov-Schlaggar.
31. White matter and neurodevelopmental disorders: honoring Jean De Vellis through the work of the NICHD-funded intellectual and developmental disabilities research centers
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Heather Cody Hazlett, Vittorio Gallo.
32. The impact of expressive language development and the left inferior longitudinal fasciculus on listening and reading comprehension
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Stephanie N. Del Tufo, F. Sayako Earle.
33. Early white matter development is abnormal in tuberous sclerosis complex patients who develop autism spectrum disorder
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Anna K. Prohl, Benoit Scherrer.
34. Spatiotemporal development of spinal neuronal and glial populations in the Ts65Dn mouse model of Down syndrome
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Nadine M. Aziz, Jenny A. Klein, Morgan R. Brady.
35. Reducing Th2 inflammation through neutralizing IL-4 antibody rescues myelination in IUGR rat brain
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Allison E. Zanno, Micah A. Romer, Lauren Fox.
36. White matter as a monitoring biomarker for neurodevelopmental disorder intervention studies
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Meghan R. Swanson, Heather C. Hazlett.
37. A diffusion-weighted imaging tract-based spatial statistics study of autism spectrum disorder in preschool-aged children
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Derek Sayre Andrews, Joshua K. Lee.
38. Are there shared neural correlates between dyslexia and ADHD? A meta-analysis of voxel-based morphometry studies
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Lauren M. McGrath, Catherine J. Stoodley.
39. The role of glia in epilepsy, intellectual disability, and other neurodevelopmental disorders in tuberous sclerosis complex
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Michael Wong.
40. Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination
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Amena Smith Fine, Christina L. Nemeth.
41. In memory of Jean de Vellis (1935–2018)
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Susan Y. Bookheimer, Harley I. Kornblum.
42. Refining the concept of GFAP toxicity in Alexander disease
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Tác giả
Albee Messing.
