"Language 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.
Conditions characterized by deficiencies of comprehension or expression of written and spoken forms of language. These include acquired and developmental disorders.
| Descriptor ID |
D007806
|
| MeSH Number(s) |
C10.597.606.150.500 C23.888.592.604.150.500
|
| Concept/Terms |
Acquired Language Disorders- Acquired Language Disorders
- Acquired Language Disorder
- Language Disorder, Acquired
- Language Disorders, Acquired
|
Below are MeSH descriptors whose meaning is more general than "Language Disorders".
Below are MeSH descriptors whose meaning is more specific than "Language Disorders".
This graph shows the total number of publications written about "Language Disorders" by people in this website by year, and whether "Language Disorders" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1998 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2005 | 0 | 2 | 2 |
| 2007 | 2 | 0 | 2 |
| 2009 | 1 | 1 | 2 |
| 2010 | 0 | 1 | 1 |
| 2011 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Language Disorders" by people in Profiles.
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Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. J Med Genet. 2024 05 21; 61(6):578-585.
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In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2. J Med Genet. 2023 06; 60(6):597-607.
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Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population. Pediatrics. 2016 04; 137(4).
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Effects of age on white matter integrity and negative symptoms in schizophrenia. Schizophr Res. 2015 Jan; 161(1):29-35.
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Searching for Potocki-Lupski syndrome phenotype: a patient with language impairment and no autism. Brain Dev. 2012 Sep; 34(8):700-3.
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Predictors of performance on the MMSE and the DRS-2 among American Indian elders. J Neuropsychiatry Clin Neurosci. 2010; 22(4):417-25.
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Relationship between neuropsychological outcome and DBS surgical trajectory and electrode location. J Neurol Sci. 2009 Dec 15; 287(1-2):159-71.
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Speaking genes or genes for speaking? Deciphering the genetics of speech and language. J Child Psychol Psychiatry. 2009 Jan; 50(1-2):116-25.
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Comparison of the validity of direct pediatric developmental evaluation versus developmental screening by parent report. Clin Pediatr (Phila). 2007 Jul; 46(6):523-9.
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Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review. Am J Med Genet A. 2007 Apr 15; 143A(8):791-8.