"Psychomotor Disorders" 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.
Abnormalities of motor function that are associated with organic and non-organic cognitive disorders.
| Descriptor ID |
D011596
|
| MeSH Number(s) |
C10.597.606.881 C23.888.592.604.882 F01.700.875
|
| Concept/Terms |
Developmental Psychomotor Disorders- Developmental Psychomotor Disorders
- Developmental Psychomotor Disorder
- Psychomotor Disorder, Developmental
- Psychomotor Disorders, Developmental
Psychomotor Impairment- Psychomotor Impairment
- Impairment, Psychomotor
- Impairments, Psychomotor
- Psychomotor Impairments
|
Below are MeSH descriptors whose meaning is more general than "Psychomotor Disorders".
Below are MeSH descriptors whose meaning is more specific than "Psychomotor Disorders".
This graph shows the total number of publications written about "Psychomotor Disorders" by people in this website by year, and whether "Psychomotor Disorders" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 1999 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2001 | 0 | 1 | 1 |
| 2007 | 1 | 1 | 2 |
| 2008 | 1 | 0 | 1 |
| 2010 | 0 | 1 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 1 | 2 |
| 2017 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Psychomotor Disorders" by people in Profiles.
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Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms. Mol Genet Genomic Med. 2021 10; 9(10):e1809.
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Disturbed phospholipid metabolism in serine biosynthesis defects revealed by metabolomic profiling. Mol Genet Metab. 2018 03; 123(3):309-316.
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Perioperative risk factors for impaired neurodevelopment after cardiac surgery in early infancy. Arch Dis Child. 2016 11; 101(11):1010-1016.
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Whole exome sequencing identifies the first STRADA point mutation in a patient with polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome (PMSE). Am J Med Genet A. 2016 08; 170(8):2181-5.
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Special topics in procedural sedation: clinical challenges and psychomotor recovery. Gastrointest Endosc. 2014 Sep; 80(3):404-9.
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Extracellular norepinephrine clearance by the norepinephrine transporter is required for skeletal homeostasis. J Biol Chem. 2013 Oct 18; 288(42):30105-30113.
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The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanisms. Hum Mutat. 2012 Nov; 33(11):1520-5.
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Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes. Nature. 2010 Nov 11; 468(7321):263-9.
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Mozart's movements and behaviour: a case of Tourette's syndrome? Postgrad Med J. 2008 Jun; 84(992):313-7.
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Anticonvulsants for the treatment of behavioral and psychological symptoms of dementia: a literature review. Int Psychogeriatr. 2008 Apr; 20(2):293-308.