"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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Sex-Specific Genetic Susceptibility to Adverse Neurodevelopmental Outcome in Offspring of Pregnancies at Risk of Early Preterm Delivery. Am J Perinatol. 2020 02; 37(3):281-290.
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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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Contribution of tactile dysfunction to manual motor dysfunction in type II diabetes. Muscle Nerve. 2016 11; 54(5):895-902.
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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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Initial Development of a Modified Trail Making Test for Individuals with Impaired Manual Functioning. Appl Neuropsychol Adult. 2016; 23(2):141-50.
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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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Microvascular brain pathology and late-life motor impairment. Neurology. 2013 Feb 19; 80(8):712-8.