"Brain Diseases" 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.
Pathologic conditions affecting the BRAIN, which is composed of the intracranial components of the CENTRAL NERVOUS SYSTEM. This includes (but is not limited to) the CEREBRAL CORTEX; intracranial white matter; BASAL GANGLIA; THALAMUS; HYPOTHALAMUS; BRAIN STEM; and CEREBELLUM.
| Descriptor ID |
D001927
|
| MeSH Number(s) |
C10.228.140
|
| Concept/Terms |
Brain Diseases- Brain Diseases
- Brain Disease
- Brain Disorders
- Brain Disorder
- Intracranial CNS Disorders
- Central Nervous System Intracranial Disorders
- CNS Disorders, Intracranial
- CNS Disorder, Intracranial
- Intracranial CNS Disorder
- Encephalon Diseases
- Encephalon Disease
- Intracranial Central Nervous System Disorders
- Central Nervous System Disorders, Intracranial
|
Below are MeSH descriptors whose meaning is more general than "Brain Diseases".
Below are MeSH descriptors whose meaning is more specific than "Brain Diseases".
This graph shows the total number of publications written about "Brain Diseases" by people in this website by year, and whether "Brain Diseases" 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 |
|---|
| 1995 | 1 | 0 | 1 |
| 1998 | 0 | 1 | 1 |
| 2004 | 1 | 0 | 1 |
| 2006 | 0 | 1 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 2 | 0 | 2 |
| 2011 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2015 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 2 | 0 | 2 |
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click here.
Below are the most recent publications written about "Brain Diseases" by people in Profiles.
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Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395).
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Brain-injured Survivors of Monochorionic Twin Pregnancies Complicated by Single Intrauterine Death: MR Findings in a Multicenter Study. Radiology. 2018 08; 288(2):582-590.
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Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features. Brain. 2017 Nov 01; 140(11):2879-2894.
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Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasia. Brain. 2015 Nov; 138(Pt 11):3238-50.
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Neu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathway. Am J Hum Genet. 2014 Sep 04; 95(3):285-93.
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Association of nephrotic syndrome with immune reconstitution inflammatory syndrome. Pediatr Nephrol. 2012 Apr; 27(4):667-9.
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Magnetization transfer imaging provides no evidence of demyelination in methotrexate-induced encephalopathy. AJNR Am J Neuroradiol. 2011 Jun-Jul; 32(6):E110-2.
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Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Gouti?res syndrome. Arthritis Rheum. 2010 May; 62(5):1469-77.
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RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection. Nat Genet. 2009 Jul; 41(7):773-5.
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Prenatal ultrasound diagnosis, follow-up, and outcome of congenital varicella syndrome. Fetal Diagn Ther. 2006; 21(3):296-301.
MeSH information
