Child Development Disorders, Pervasive
"Child Development Disorders, Pervasive" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Severe distortions in the development of many basic psychological functions that are not normal for any stage in development. These distortions are manifested in sustained social impairment, speech abnormalities, and peculiar motor movements.
Descriptor ID |
D002659
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MeSH Number(s) |
F03.625.164
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Child Development Disorders, Pervasive".
Below are MeSH descriptors whose meaning is more specific than "Child Development Disorders, Pervasive".
This graph shows the total number of publications written about "Child Development Disorders, Pervasive" by people in this website by year, and whether "Child Development Disorders, Pervasive" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2009 | 1 | 0 | 1 |
2010 | 1 | 0 | 1 |
2011 | 5 | 1 | 6 |
2012 | 4 | 0 | 4 |
2013 | 2 | 3 | 5 |
2014 | 5 | 1 | 6 |
2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Child Development Disorders, Pervasive" by people in Profiles.
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Editorial: Analyzing Treatment and Prescribing in Large Administrative Datasets With a Lens on Equity. J Am Acad Child Adolesc Psychiatry. 2021 07; 60(7):818-820.
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Fragile X syndrome: a review of associated medical problems. Pediatrics. 2014 Nov; 134(5):995-1005.
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Melatonin in children with autism spectrum disorders: endogenous and pharmacokinetic profiles in relation to sleep. J Autism Dev Disord. 2014 Oct; 44(10):2525-35.
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The challenges of clinical trials in fragile X syndrome. Psychopharmacology (Berl). 2014 Mar; 231(6):1237-50.
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Therapeutic strategies in fragile X syndrome: dysregulated mGluR signaling and beyond. Neuropsychopharmacology. 2012 Jan; 37(1):178-95.
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Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain. FASEB J. 2010 Aug; 24(8):3036-51.