"Child, Preschool" 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.
A child between the ages of 2 and 5.
Descriptor ID |
D002675
|
MeSH Number(s) |
M01.060.406.448
|
Concept/Terms |
Child, Preschool- Child, Preschool
- Preschool Child
- Children, Preschool
- Preschool Children
|
Below are MeSH descriptors whose meaning is more general than "Child, Preschool".
Below are MeSH descriptors whose meaning is more specific than "Child, Preschool".
This graph shows the total number of publications written about "Child, Preschool" by people in this website by year, and whether "Child, Preschool" 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 |
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1995 | 0 | 1 | 1 |
1996 | 0 | 3 | 3 |
1997 | 0 | 3 | 3 |
1998 | 0 | 1 | 1 |
1999 | 0 | 1 | 1 |
2000 | 0 | 2 | 2 |
2001 | 0 | 3 | 3 |
2002 | 0 | 3 | 3 |
2003 | 0 | 6 | 6 |
2004 | 0 | 5 | 5 |
2005 | 0 | 4 | 4 |
2006 | 0 | 7 | 7 |
2007 | 0 | 9 | 9 |
2008 | 0 | 7 | 7 |
2009 | 0 | 11 | 11 |
2010 | 0 | 18 | 18 |
2011 | 0 | 15 | 15 |
2012 | 0 | 24 | 24 |
2013 | 0 | 23 | 23 |
2014 | 0 | 28 | 28 |
2015 | 0 | 26 | 26 |
2016 | 0 | 19 | 19 |
2017 | 0 | 27 | 27 |
2018 | 0 | 31 | 31 |
2019 | 0 | 22 | 22 |
2020 | 0 | 14 | 14 |
2021 | 0 | 21 | 21 |
2022 | 0 | 1 | 1 |
2023 | 0 | 4 | 4 |
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click here.
Below are the most recent publications written about "Child, Preschool" by people in Profiles.
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Natural History and Developmental Trajectories of Individuals With Disease-Causing Variants in STXBP1. Neurology. 2023 08 29; 101(9):e879-e891.
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Delineating disorder-general and disorder-specific dimensions of psychopathology from functional brain networks in a developmental clinical sample. Dev Cogn Neurosci. 2023 08; 62:101271.
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Identification of a novel sporadic U2HR pathogenic variant in a patient with Marie Unna hereditary hypotrichosis. Pediatr Dermatol. 2023 May-Jun; 40(3):466-467.
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Shared pattern of impaired social communication and cognitive ability in the youth brain across diagnostic boundaries. Dev Cogn Neurosci. 2023 04; 60:101219.
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Patterns and temporal trends in the incidence of childhood and adolescence cancer in Cyprus 1998-2017: A population-based study from the Cyprus Paediatric Oncology Registry. Cancer Epidemiol. 2022 10; 80:102239.
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Toward prevention of childhood ALL by early-life immune training. Blood. 2021 10 21; 138(16):1412-1428.
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The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype. J Mol Med (Berl). 2021 12; 99(12):1755-1768.
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MFSD2A-associated primary microcephaly - Expanding the clinical and mutational spectrum of this ultra-rare disease. Eur J Med Genet. 2021 Oct; 64(10):104310.
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Neurodevelopmental Profile in Children Affected by Ocular Albinism. Neuropediatrics. 2022 02; 53(1):7-14.
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Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes. Am J Med Genet A. 2021 12; 185(12):3900-3904.