Found: 11
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Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility.
- Published in:
- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.858238
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- Publication type:
- Article
Neuropsychiatric phenotype in a child with pseudohypoparathyroidism.
- Published in:
- 2016
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- Publication type:
- Case Study
Is cognitive behavioural therapy an effective complement to antidepressants in adolescents? A meta-analysis.
- Published in:
- Acta Neuropsychiatrica, 2011, v. 23, n. 6, p. 263, doi. 10.1111/j.1601-5215.2011.00595.x
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- Publication type:
- Article
Brain Magnetic Resonance Findings in 117 Children with Autism Spectrum Disorder under 5 Years Old.
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- Brain Sciences (2076-3425), 2020, v. 10, n. 10, p. 741, doi. 10.3390/brainsci10100741
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- Publication type:
- Article
Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.953762
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- Publication type:
- Article
Methyl-CpG-binding Protein 2 (MECP2) Gene Mutations in an Italian Sample of Patients With Pervasive Developmental Disorder and Mental Retardation.
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- Journal of Child Neurology, 2009, v. 24, n. 6, p. 772, doi. 10.1177/0883073808327834
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- Publication type:
- Article
Cerebellar Hypoplasia, Continuous Spike-waves During Sleep, and Neuropsychological and Behavioral Disorders.
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- Journal of Child Neurology, 2008, v. 23, n. 12, p. 1472, doi. 10.1177/0883073808319077
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- Publication type:
- Article
Epilepsy in Patients With Pervasive Developmental Disorder Not Otherwise Specified.
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- Journal of Child Neurology, 2007, v. 22, n. 10, p. 1198, doi. 10.1177/0883073807306265
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- Publication type:
- Article
Epilepsy, Intelligence, and Psychiatric Disorders in Patients With Cerebellar Hypoplasia.
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- Journal of Child Neurology, 2003, v. 18, n. 1, p. 1, doi. 10.1177/08830738030180011001
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- Publication type:
- Article
Posterior Fossa Malformations and Epilepsy.
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- Journal of Child Neurology, 1999, v. 14, n. 2, p. 113, doi. 10.1177/088307389901400209
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- Publication type:
- Article
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates.
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- NPJ Genomic Medicine, 2024, v. 9, n. 1, p. 1, doi. 10.1038/s41525-024-00411-1
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- Publication type:
- Article