Ausgabe 1/2019
Inhalt (41 Artikel)
Differentiating social preference and social anxiety phenotypes in fragile X syndrome using an eye gaze analysis: a pilot study
Michael P. Hong, Eleanor M. Eckert, Ernest V. Pedapati, Rebecca C. Shaffer, Kelli C. Dominick, Logan K. Wink, John A. Sweeney, Craig A. Erickson
Static and dynamic postural control deficits in aging fragile X mental retardation 1 (FMR1) gene premutation carriers
Zheng Wang, Pravin Khemani, Lauren M. Schmitt, Su Lui, Matthew W. Mosconi
Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
Gregory Costain, Susan Walker, Bob Argiropoulos, Danielle A. Baribeau, Anne S. Bassett, Erik Boot, Koen Devriendt, Barbara Kellam, Christian R. Marshall, Aparna Prasad, Moises A. Serrano, D. James Stavropoulos, Hope Twede, Joris R. Vermeesch, Jacob A. S. Vorstman, Stephen W. Scherer
Cognitive training for children and adolescents with fragile X syndrome: a randomized controlled trial of Cogmed
David Hessl, Julie B. Schweitzer, Danh V. Nguyen, Yingratana A. McLennan, Cindy Johnston, Ryan Shickman, Yanjun Chen
Adaptation to different communicative contexts: an eye tracking study of autistic adults
Julia Parish-Morris, Ashley A. Pallathra, Emily Ferguson, Brenna B. Maddox, Alison Pomykacz, Leat S. Perez, Leila Bateman, Juhi Pandey, Robert T. Schultz, Edward S. Brodkin
Lifespan trajectory of affect in Cornelia de Lange syndrome: towards a neurobiological hypothesis
Laura Groves, Joanna Moss, Hayley Crawford, Lisa Nelson, Chris Stinton, Gursharan Singla, Chris Oliver
In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
Zahra Motahari, Sally Ann Moody, Thomas Michael Maynard, Anthony-Samuel LaMantia
Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion syndrome
Adam C. Cunningham, Liam Hill, Mark Mon-Williams, Kathryn J. Peall, David E. J. Linden, Jeremy Hall, Michael J. Owen, Marianne B. M. van den Bree
Lesser suppression of response to bright visual stimuli and visual abnormality in children with autism spectrum disorder: a magnetoencephalographic study
Sho Aoki, Kuriko Kagitani-Shimono, Junko Matsuzaki, Ryuzo Hanaie, Mariko Nakanishi, Koji Tominaga, Yukie Nagai, Ikuko Mohri, Masako Taniike
Impaired neurodevelopmental pathways in autism spectrum disorder: a review of signaling mechanisms and crosstalk
Santosh Kumar, Kurt Reynolds, Yu Ji, Ran Gu, Sunil Rai, Chengji J. Zhou
Novel pathogenic variants and multiple molecular diagnoses in neurodevelopmental disorders
Joanne Trinh, Krishna Kumar Kandaswamy, Martin Werber, Maximilian E. R. Weiss, Gabriela Oprea, Shivendra Kishore, Katja Lohmann, Arndt Rolfs
Children with facial paralysis due to Moebius syndrome exhibit reduced autonomic modulation during emotion processing
Elisa De Stefani, Martina Ardizzi, Ylenia Nicolini, Mauro Belluardo, Anna Barbot, Chiara Bertolini, Gioacchino Garofalo, Bernardo Bianchi, Gino Coudé, Lynne Murray, Pier Francesco Ferrari
A Brazilian cohort of individuals with Phelan-McDermid syndrome: genotype-phenotype correlation and identification of an atypical case
Claudia Ismania Samogy-Costa, Elisa Varella-Branco, Frederico Monfardini, Helen Ferraz, Rodrigo Ambrósio Fock, Ricardo Henrique Almeida Barbosa, André Luiz Santos Pessoa, Ana Beatriz Alvarez Perez, Naila Lourenço, Maria Vibranovski, Ana Krepischi, Carla Rosenberg, Maria Rita Passos-Bueno
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
Rachael Bedford, Teodora Gliga, Alexandra Hendry, Emily J. H. Jones, Greg Pasco, Tony Charman, Mark H. Johnson, Andrew Pickles, Simon Baron-Cohen, Patrick Bolton, Bosiljka Milosavljevic, Susie Chandler, Mayada Elsabbagh, Janice Fernandes, Holly Garwood, Kristelle Hudry, Elizabeth Shephard, Leslie Tucker, Agnes Volein
Electroencephalographic spectral power as a marker of cortical function and disease severity in girls with Rett syndrome
Katherine J. Roche, Jocelyn J. LeBlanc, April R. Levin, Heather M. O’Leary, Lauren M. Baczewski, Charles A. Nelson
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
Helen Heussler, Jonathan Cohen, Natalie Silove, Nancy Tich, Marcel O. Bonn-Miller, Wei Du, Carol O’Neill, Terri Sebree
STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics
Sinéad O’Brien, Elise Ng-Cordell, Duncan E. Astle, Gaia Scerif, Kate Baker
Phenotypic characterization of individuals with SYNGAP1 pathogenic variants reveals a potential correlation between posterior dominant rhythm and developmental progression
Andres Jimenez-Gomez, Sizhe Niu, Fabiola Andujar-Perez, Elizabeth A. McQuade, Alfred Balasa, David Huss, Rohini Coorg, Michael Quach, Sherry Vinson, Sarah Risen, J. Lloyd Holder Jr
Magnetoencephalographic (MEG) brain activity during a mental flexibility task suggests some shared neurobiology in children with neurodevelopmental disorders
Alexandra Mogadam, Anne E. Keller, Paul D. Arnold, Russell Schachar, Jason P. Lerch, Evdokia Anagnostou, Elizabeth W. Pang
Assessing general cognitive and adaptive abilities in adults with Down syndrome: a systematic review
Sarah Hamburg, Bryony Lowe, Carla Marie Startin, Concepcion Padilla, Antonia Coppus, Wayne Silverman, Juan Fortea, Shahid Zaman, Elizabeth Head, Benjamin L. Handen, Ira Lott, Weihong Song, André Strydom
Within-task variability on standardized language tests predicts autism spectrum disorder: a pilot study of the Response Dispersion Index
Abby E. Hare-Harris, Marissa W. Mitchel, Scott M. Myers, Aaron D. Mitchel, Brian R. King, Brittany G. Ruocco, Christa Lese Martin, Judy F. Flax, Linda M. Brzustowicz
Early negative affect in males and females with fragile X syndrome: implications for anxiety and autism
Carla A. Wall, Abigail L. Hogan, Elizabeth A. Will, Samuel McQuillin, Bridgette L. Kelleher, Jane E. Roberts
Developmental divergence: motor trajectories in children with fragile X syndrome with and without co-occurring autism
Elizabeth A. Will, Somer L. Bishop, Jane E. Roberts
Behavioural and psychological characteristics in Pitt-Hopkins syndrome: a comparison with Angelman and Cornelia de Lange syndromes
Alice Watkins, Stacey Bissell, Jo Moss, Chris Oliver, Jill Clayton-Smith, Lorraine Haye, Mary Heald, Alice Welham
Vocabulary comprehension in adults with fragile X syndrome (FXS)
Anne Hoffmann, Sue Ellen Krause, Joanne Wuu, Sue Leurgans, Stephen J. Guter Jr, Sandra S. Block, Jeff Salt, Edwin Cook Jr, Dominick M. Maino, Elizabeth Berry-Kravis
Quantitative gait assessment in children with 16p11.2 syndrome
Sylvie Goldman, Aston K. McCullough, Sally Dunaway Young, Carly Mueller, Adrianna Stahl, Audrey Zoeller, Laurel Daniels Abbruzzese, Ashwini K. Rao, Jacqueline Montes
In memory of Jean de Vellis (1935–2018)
Susan Y. Bookheimer, Harley I. Kornblum
Mitochondrial aminoacyl-tRNA synthetase disorders: an emerging group of developmental disorders of myelination
Amena Smith Fine, Christina L. Nemeth, Miriam L. Kaufman, Ali Fatemi
The role of glia in epilepsy, intellectual disability, and other neurodevelopmental disorders in tuberous sclerosis complex
Michael Wong
Are there shared neural correlates between dyslexia and ADHD? A meta-analysis of voxel-based morphometry studies
Lauren M. McGrath, Catherine J. Stoodley
A diffusion-weighted imaging tract-based spatial statistics study of autism spectrum disorder in preschool-aged children
Derek Sayre Andrews, Joshua K. Lee, Marjorie Solomon, Sally J. Rogers, David G. Amaral, Christine Wu Nordahl
White matter as a monitoring biomarker for neurodevelopmental disorder intervention studies
Meghan R. Swanson, Heather C. Hazlett
Reducing Th2 inflammation through neutralizing IL-4 antibody rescues myelination in IUGR rat brain
Allison E. Zanno, Micah A. Romer, Lauren Fox, Thea Golden, Lane Jaeckle-Santos, Rebecca A. Simmons, Judith B. Grinspan
Spatiotemporal development of spinal neuronal and glial populations in the Ts65Dn mouse model of Down syndrome
Nadine M. Aziz, Jenny A. Klein, Morgan R. Brady, Jose Luis Olmos-Serrano, Vittorio Gallo, Tarik F. Haydar
Early white matter development is abnormal in tuberous sclerosis complex patients who develop autism spectrum disorder
Anna K. Prohl, Benoit Scherrer, Xavier Tomas-Fernandez, Peter E. Davis, Rajna Filip-Dhima, Sanjay P. Prabhu, Jurriaan M. Peters, E. Martina Bebin, Darcy A. Krueger, Hope Northrup, Joyce Y. Wu, Mustafa Sahin, Simon K. Warfield, Simon K. Warfield, Jurriaan M. Peters, Monisha Goyal, Deborah A. Pearson, Marian E. Williams, Ellen Hanson, Nicole Bing, Bridget Kent, Sarah O’Kelley, Rajna Filip-Dhima, Kira Dies, Stephanie Bruns, Benoit Scherrer, Gary Cutter, Donna S. Murray, Steven L. Roberds
White matter and neurodevelopmental disorders: honoring Jean De Vellis through the work of the NICHD-funded intellectual and developmental disabilities research centers
Heather Cody Hazlett, Vittorio Gallo
Adaptation of the Clinical Dementia Rating Scale for adults with Down syndrome
Christina N. Lessov-Schlaggar, Olga L. del Rosario, John C. Morris, Beau M. Ances, Bradley L. Schlaggar, John N. Constantino
Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome
Kathryn L. McCabe, Abbie M. Popa, Courtney Durdle, Michele Amato, Margarita H. Cabaral, Joshua Cruz, Ling M. Wong, Danielle Harvey, Nicole Tartaglia, Tony J. Simon
Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome
Emma K. Baker, Marta Arpone, Solange Aliaga Vera, Lesley Bretherton, Alexandra Ure, Claudine M. Kraan, Minh Bui, Ling Ling, David Francis, Matthew F. Hunter, Justine Elliott, Carolyn Rogers, Michael J. Field, Jonathan Cohen, Lorena Santa Maria, Victor Faundes, Bianca Curotto, Paulina Morales, Cesar Trigo, Isabel Salas, Angelica M. Alliende, David J. Amor, David E. Godler
Initial eye gaze to faces and its functional consequence on face identification abilities in autism spectrum disorder
Kimberly B. Schauder, Woon Ju Park, Yuliy Tsank, Miguel P. Eckstein, Duje Tadin, Loisa Bennetto