Works matching IS 18661947 AND DT 2013 AND VI 5 AND IP 1
Results: 18
Examining associations between anxiety and cortisol in high functioning male children with autism.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-32
- By:
- Publication type:
- Article
Divergent structural brain abnormalities between different genetic subtypes of children with Prader--Willi syndrome.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-31
- By:
- Publication type:
- Article
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-29
- By:
- Publication type:
- Article
Eye tracking in early autism research.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-28
- By:
- Publication type:
- Article
Prevalence of selected clinical problems in older adults with autism and intellectual disability.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-27
- By:
- Publication type:
- Article
Sensory and motor secondary symptoms as indicators of brain vulnerability.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-26
- By:
- Publication type:
- Article
The broad autism phenotype predicts child functioning in autism spectrum disorders.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-25
- By:
- Publication type:
- Article
Resting state EEG abnormalities in autism spectrum disorders.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-24
- By:
- Publication type:
- Article
Methotrexate treatment of FraX fibroblasts results in FMR1 transcription but not in detectable FMR1 protein levels.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-23
- By:
- Publication type:
- Article
Developmental maturation of astrocytes and pathogenesis of neurodevelopmental disorders.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-22
- By:
- Publication type:
- Article
Intracranial arachnoid cysts: impairment of higher cognitive functions and postoperative improvement.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-21
- By:
- Publication type:
- Article
Aberrant basal ganglia metabolism in fragile X syndrome: a magnetic resonance spectroscopy study.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-20
- By:
- Publication type:
- Article
Dementia in Down's syndrome: an MRI comparison with Alzheimer's disease in the general population.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-19
- By:
- Publication type:
- Article
Behavioral profile of adults with Prader-Willi syndrome: correlations with individual and environmental variables.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-18
- By:
- Publication type:
- Article
Spontaneous and cued gaze-following in autism and Williams syndrome.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-13
- By:
- Publication type:
- Article
The effect of chronic prenatal hypoxia on the development of mature neurons in the cerebellum.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-17
- By:
- Publication type:
- Article
Organization of brain networks governed by long-range connections index autistic traits in the general population.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-16
- By:
- Publication type:
- Article
Comparative DNA methylation among females with neurodevelopmental disorders and seizures identifies TAC1 as a MeCP2 target gene.
- Published in:
- Journal of Neurodevelopmental Disorders, 2013, v. 5, n. 1, p. 1, doi. 10.1186/1866-1955-5-15
- By:
- Publication type:
- Article