 Language Disorders
"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
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| MeSH Number(s) |
C10.597.606.150.500 C23.888.592.604.150.500
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| Concept/Terms |
Acquired Language Disorders- Acquired Language Disorders
- Acquired Language Disorder
- Language Disorder, Acquired
- Language Disorders, Acquired
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 1 | 0 | 1 | | 2003 | 1 | 0 | 1 | | 2008 | 0 | 1 | 1 | | 2013 | 0 | 1 | 1 | | 2015 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Language Disorders" by people in Profiles.
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Witton C, Eckert MA, Stanford IM, Gascoyne LE, Furlong PL, Worthen SF, Hillebrand A. The auditory evoked-gamma response and its relation with the N1m. Hear Res. 2017 05; 348:78-86.
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Adhikari MH, Raja Beharelle A, Griffa A, Hagmann P, Solodkin A, McIntosh AR, Small SL, Deco G. Computational modeling of resting-state activity demonstrates markers of normalcy in children with prenatal or perinatal stroke. J Neurosci. 2015 Jun 10; 35(23):8914-24.
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Berry-Kravis E, Doll E, Sterling A, Kover ST, Schroeder SM, Mathur S, Abbeduto L. Development of an expressive language sampling procedure in fragile X syndrome: a pilot study. J Dev Behav Pediatr. 2013 May; 34(4):245-51.
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Rice GM, Raca G, Jakielski KJ, Laffin JJ, Iyama-Kurtycz CM, Hartley SL, Sprague RE, Heintzelman AT, Shriberg LD. Phenotype of FOXP2 haploinsufficiency in a mother and son. Am J Med Genet A. 2012 Jan; 158A(1):174-81.
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Prabhakaran S, Silver AJ, Warrior L, McClenathan B, Lee VH. Misdiagnosis of transient ischemic attacks in the emergency room. Cerebrovasc Dis. 2008; 26(6):630-5.
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Leonard CM, Eckert MA, Kuldau JM. Exploiting human anatomical variability as a link between genome and cognome. Genes Brain Behav. 2006; 5 Suppl 1:64-77.
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Ovsiew F. Yes/no reversals. Eur J Neurol. 2003 Jul; 10(4):464; author reply 464.
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Reichenberg A, Weiser M, Rabinowitz J, Caspi A, Schmeidler J, Mark M, Kaplan Z, Davidson M. A population-based cohort study of premorbid intellectual, language, and behavioral functioning in patients with schizophrenia, schizoaffective disorder, and nonpsychotic bipolar disorder. Am J Psychiatry. 2002 Dec; 159(12):2027-35.
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Leonard CM, Lombardino LJ, Walsh K, Eckert MA, Mockler JL, Rowe LA, Williams S, DeBose CB. Anatomical risk factors that distinguish dyslexia from SLI predict reading skill in normal children. J Commun Disord. 2002 Nov-Dec; 35(6):501-31.
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Eckert MA, Leonard CM, Molloy EA, Blumenthal J, Zijdenbos A, Giedd JN. The epigenesis of planum temporale asymmetry in twins. Cereb Cortex. 2002 Jul; 12(7):749-55.
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