Ausgabe 1/2013
Inhalt (32 Artikel)
The regulatory function of social referencing in preschoolers with Down syndrome or Williams syndrome
Angela John Thurman, Carolyn B Mervis
Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteins
Junlin Li, Guifang Zhao, Xiaocai Gao
Gyrification, cortical and subcortical morphometry in neurofibromatosis type 1: an uneven profile of developmental abnormalities
Inês R Violante, Maria J Ribeiro, Eduardo D Silva, Miguel Castelo-Branco
Journal of Neurodevelopmental Disorders reviewer acknowledgement 2012
Joseph Piven
Using infrared eye-tracking to explore ordinal numerical processing in toddlers with Fragile X Syndrome
Emily R Owen, Heidi A Baumgartner, Susan M Rivera
Neurodevelopmental alcohol exposure elicits long-term changes to gene expression that alter distinct molecular pathways dependent on timing of exposure
Morgan L Kleiber, Katarzyna Mantha, Randa L Stringer, Shiva M Singh
A quantitative homogeneous assay for fragile X mental retardation 1 protein
Gabi Schutzius, Dorothee Bleckmann, Sandra Kapps-Fouthier, Francesco di Giorgio, Bernd Gerhartz, Andreas Weiss
Social and emotional processing in Prader-Willi syndrome: genetic subtype differences
Alexandra P Key, Dorita Jones, Elisabeth M Dykens
Autism and the broad autism phenotype: familial patterns and intergenerational transmission
Noah J Sasson, Kristen SL Lam, Morgan Parlier, Julie L Daniels, Joseph Piven
Repetitive and self-injurious behaviors: associations with caudate volume in autism and fragile X syndrome
Jason J Wolff, Heather C Hazlett, Amy A Lightbody, Allan L Reiss, Joseph Piven
A pilot open-label trial of minocycline in patients with autism and regressive features
Carlos A Pardo, Ashura Buckley, Audrey Thurm, Li-Ching Lee, Arun Azhagiri, David M Neville, Susan E Swedo
Developmental patterns of DR6 in normal human hippocampus and in Down syndrome
Anand Iyer, Jackelien van Scheppingen, Jasper Anink, Ivan Milenkovic, Gabor G Kovács, Eleonora Aronica
Working memory deficits in high-functioning adolescents with autism spectrum disorders: neuropsychological and neuroimaging correlates
Evelien M Barendse, Marc PH Hendriks, Jacobus FA Jansen, Walter H Backes, Paul AM Hofman, Geert Thoonen, Roy PC Kessels, Albert P Aldenkamp
Organization of brain networks governed by long-range connections index autistic traits in the general population
Pablo Barttfeld, Lucía Amoruso, Joaquín Ais, Sebastián Cukier, Luz Bavassi, Ailin Tomio, Facundo Manes, Agustín Ibanez, Mariano Sigman
Comparative DNA methylation among females with neurodevelopmental disorders and seizures identifies TAC1 as a MeCP2 target gene
Kimberly A Aldinger, Jasmine T Plummer, Pat Levitt
The effect of chronic prenatal hypoxia on the development of mature neurons in the cerebellum
Keumyoung So, Yoonyoung Chung, Hyunyoung Lee, Eunyoung Kim, Yonghyun Jeon
Behavioral profile of adults with Prader-Willi syndrome: correlations with individual and environmental variables
Joseba Jauregi, Virginie Laurier, Pierre Copet, Maithé Tauber, Denise Thuilleaux
Dementia in Down’s syndrome: an MRI comparison with Alzheimer’s disease in the general population
Diane Mullins, Eileen Daly, Andrew Simmons, Felix Beacher, Catherine ML Foy, Simon Lovestone, Brian Hallahan, Kieran C Murphy, Declan G Murphy
Developmental maturation of astrocytes and pathogenesis of neurodevelopmental disorders
Yongjie Yang, Haruki Higashimori, Lydie Morel
Intracranial arachnoid cysts: impairment of higher cognitive functions and postoperative improvement
Priyanthi B Gjerde, Marit Schmid, Åsa Hammar, Knut Wester
Spontaneous and cued gaze-following in autism and Williams syndrome
Deborah M Riby, Peter JB Hancock, Nicola Jones, Mary Hanley
Methotrexate treatment of FraX fibroblasts results in FMR1 transcription but not in detectable FMR1 protein levels
Cornelia Brendel, Benjamin Mielke, Merle Hillebrand, Jutta Gärtner, Peter Huppke
Aberrant basal ganglia metabolism in fragile X syndrome: a magnetic resonance spectroscopy study
Jennifer Lynn Bruno, Elizabeth Walter Shelly, Eve-Marie Quintin, Maryam Rostami, Sweta Patnaik, Daniel Spielman, Dirk Mayer, Meng Gu, Amy A Lightbody, Allan L Reiss
Resting state EEG abnormalities in autism spectrum disorders
Jun Wang, Jamie Barstein, Lauren E Ethridge, Matthew W Mosconi, Yukari Takarae, John A Sweeney
The broad autism phenotype predicts child functioning in autism spectrum disorders
Christina R Maxwell, Julia Parish-Morris, Olivia Hsin, Jennifer C Bush, Robert T Schultz
Prevalence of selected clinical problems in older adults with autism and intellectual disability
Dmitry Kats, Leslie Payne, Morgan Parlier, Joseph Piven
Eye tracking in early autism research
Terje Falck-Ytter, Sven Bölte, Gustaf Gredebäck
Sensory and motor secondary symptoms as indicators of brain vulnerability
Nava Levit-Binnun, Michael Davidovitch, Yulia Golland
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
Elizabeth A Worthey, Gordana Raca, Jennifer J Laffin, Brandon M Wilk, Jeremy M Harris, Kathy J Jakielski, David P Dimmock, Edythe A Strand, Lawrence D Shriberg
A molecular genetic study of autism and related phenotypes in extended pedigrees
Joseph Piven, Veronica J Vieland, Morgan Parlier, Ann Thompson, Irene O’Conner, Mark Woodbury-Smith, Yungui Huang, Kimberly A Walters, Bridget Fernandez, Peter Szatmari
Divergent structural brain abnormalities between different genetic subtypes of children with Prader–Willi syndrome
Akvile Lukoshe, Tonya White, Marcus N Schmidt, Aad van der Lugt, Anita C Hokken-Koelega
Examining associations between anxiety and cortisol in high functioning male children with autism
David M Simon, Blythe A Corbett