Found: 21
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Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome.
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- Journal of Neurodevelopmental Disorders, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s11689-024-09541-0
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- Article
Asperger's Syndrome and High-Functioning Autism.
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- Pediatric Annals, 2009, v. 38, n. 1, p. 30, doi. 10.3928/00904481-20090101-01
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- Article
Prospective phenotyping of CHAMP1 disorder indicates that coding mutations may not act through haploinsufficiency.
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- Human Genetics, 2023, v. 142, n. 9, p. 1385, doi. 10.1007/s00439-023-02578-6
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- Article
Measuring Sensory Reactivity in Autism Spectrum Disorder: Application and Simplification of a Clinician-Administered Sensory Observation Scale.
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- Journal of Autism & Developmental Disorders, 2016, v. 46, n. 1, p. 287, doi. 10.1007/s10803-015-2578-3
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- Article
The Autism Mental Status Exam: Sensitivity and Specificity Using DSM-5 Criteria for Autism Spectrum Disorder in Verbally Fluent Adults.
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- Journal of Autism & Developmental Disorders, 2014, v. 44, n. 3, p. 609, doi. 10.1007/s10803-013-1917-5
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- Article
Social visual attentional engagement and memory in Phelan-McDermid syndrome and autism spectrum disorder: a pilot eye tracking study.
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- Journal of Neurodevelopmental Disorders, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s11689-021-09400-2
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- Article
Psychosocial Interventions for Motor Coordination, Executive Functions, and Socialization Deficits in ADHD and ASD.
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- Primary Psychiatry, 2009, v. 16, n. 1, p. 48
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- Article
Reduced engagement of visual attention in children with autism spectrum disorder.
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- Autism: The International Journal of Research & Practice, 2021, v. 25, n. 7, p. 2064, doi. 10.1177/13623613211010072
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- Article
Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis.
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- Genes, 2021, v. 12, n. 3, p. 351, doi. 10.3390/genes12030351
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- Article
A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome.
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- Molecular Autism, 2014, v. 5, n. 1, p. 1, doi. 10.1186/2040-2392-5-54
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- Article
Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.
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- Molecular Autism, 2013, v. 4, n. 1, p. 1, doi. 10.1186/2040-2392-4-18
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- Article
Intranasal oxytocin versus placebo in the treatment of adults with autism spectrum disorders: a randomized controlled trial.
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- Molecular Autism, 2012, v. 3, n. 1, p. 16, doi. 10.1186/2040-2392-3-16
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- Article
Assessing the utility of electronic measures as a proxy for cognitive ability.
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- Autism Research: Official Journal of the International Society for Autism Research, 2022, v. 15, n. 6, p. 988, doi. 10.1002/aur.2704
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- Article
Social cognitive skills groups increase medial prefrontal cortex activity in children with autism spectrum disorder.
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- Autism Research: Official Journal of the International Society for Autism Research, 2021, v. 14, n. 12, p. 2495, doi. 10.1002/aur.2603
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- Article
Neural Markers of Auditory Response and Habituation in Phelan-McDermid Syndrome.
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- Frontiers in Neuroscience, 2022, p. 1, doi. 10.3389/fnins.2022.815933
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- Article
Individuals with FOXP1 syndrome present with a complex neurobehavioral profile with high rates of ADHD, anxiety, repetitive behaviors, and sensory symptoms.
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- Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00469-z
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- Article
Prospective and detailed behavioral phenotyping in DDX3X syndrome.
- Published in:
- Molecular Autism, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13229-021-00431-z
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- Article
Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by <italic>SHANK3</italic> point mutations.
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- Molecular Autism, 2018, v. 9, n. 1, p. N.PAG, doi. 10.1186/s13229-018-0205-9
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- Article
De novo SCN2A splice site mutation in a boy with Autism spectrum disorder.
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- BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-35
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- Article
CHAMP1 disorder is associated with a complex neurobehavioral phenotype including autism, ADHD, repetitive behaviors and sensory symptoms.
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- Human Molecular Genetics, 2022, v. 31, n. 15, p. 2582, doi. 10.1093/hmg/ddac018
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- Article
Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 625, doi. 10.1093/hmg/ddab280
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- Article