 Brain Diseases
"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
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| MeSH Number(s) |
C10.228.140
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| Concept/Terms |
Brain Diseases- Brain Diseases
- Brain Disease
- Central Nervous System Disorders, Intracranial
- Intracranial CNS Disorders
- CNS Disorders, Intracranial
- CNS Disorder, Intracranial
- Intracranial CNS Disorder
- Encephalon Diseases
- Encephalon Disease
- Intracranial Central Nervous System Disorders
- Brain Disorders
- Brain Disorder
- Central Nervous System Intracranial Disorders
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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 |
|---|
| 1980 | 1 | 0 | 1 | | 1981 | 1 | 0 | 1 | | 1982 | 1 | 0 | 1 | | 1983 | 3 | 1 | 4 | | 1984 | 1 | 0 | 1 | | 1985 | 2 | 2 | 4 | | 1986 | 1 | 1 | 2 | | 1987 | 0 | 1 | 1 | | 1988 | 5 | 0 | 5 | | 1989 | 3 | 1 | 4 | | 1990 | 3 | 1 | 4 | | 1991 | 3 | 0 | 3 | | 1992 | 2 | 3 | 5 | | 1993 | 3 | 1 | 4 | | 1994 | 2 | 0 | 2 | | 1995 | 1 | 2 | 3 | | 1996 | 3 | 0 | 3 | | 1997 | 4 | 2 | 6 | | 1998 | 3 | 1 | 4 | | 1999 | 4 | 2 | 6 | | 2000 | 9 | 2 | 11 | | 2001 | 4 | 1 | 5 | | 2003 | 4 | 1 | 5 | | 2004 | 3 | 0 | 3 | | 2005 | 2 | 1 | 3 | | 2006 | 4 | 0 | 4 | | 2007 | 4 | 1 | 5 | | 2008 | 6 | 0 | 6 | | 2009 | 4 | 0 | 4 | | 2010 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2012 | 1 | 0 | 1 | | 2013 | 4 | 2 | 6 | | 2014 | 6 | 0 | 6 | | 2015 | 5 | 1 | 6 | | 2016 | 1 | 0 | 1 | | 2017 | 6 | 0 | 6 | | 2018 | 3 | 3 | 6 | | 2019 | 2 | 0 | 2 |
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Below are the most recent publications written about "Brain Diseases" by people in Profiles.
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Oegema R, Barkovich AJ, Mancini GMS, Guerrini R, Dobyns WB. Subcortical heterotopic gray matter brain malformations: Classification study of 107 individuals. Neurology. 2019 10 01; 93(14):e1360-e1373.
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Dodiya HB, Kuntz T, Shaik SM, Baufeld C, Leibowitz J, Zhang X, Gottel N, Zhang X, Butovsky O, Gilbert JA, Sisodia SS. Sex-specific effects of microbiome perturbations on cerebral Aß amyloidosis and microglia phenotypes. J Exp Med. 2019 07 01; 216(7):1542-1560.
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Chang P, Ruff I, Mendelson SJ, Caprio F, Bergman DL, Prabhakaran S. The 2CAN Score. Stroke. 2018 12; 49(12):2866-2871.
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Ramos EM, Carecchio M, Lemos R, Ferreira J, Legati A, Sears RL, Hsu SC, Panteghini C, Magistrelli L, Salsano E, Esposito S, Taroni F, Richard AC, Tranchant C, Anheim M, Ayrignac X, Goizet C, Vidailhet M, Maltete D, Wallon D, Frebourg T, Pimentel L, Geschwind DH, Vanakker O, Galasko D, Fogel BL, Innes AM, Ross A, Dobyns WB, Alcantara D, O'Driscoll M, Hannequin D, Campion D. Primary brain calcification: an international study reporting novel variants and associated phenotypes. Eur J Hum Genet. 2018 10; 26(10):1462-1477.
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Analysis of shared heritability in common disorders of the brain. Science. 2018 06 22; 360(6395).
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Rocque BG, Agee BS, Thompson EM, Piedra M, Baird LC, Selden NR, Greene S, Deibert CP, Hankinson TC, Lew SM, Iskandar BJ, Bragg TM, Frim D, Grant G, Gupta N, Auguste KI, Nikas DC, Vassilyadi M, Muh CR, Wetjen NM, Lam SK. Complications following pediatric cranioplasty after decompressive craniectomy: a multicenter retrospective study. J Neurosurg Pediatr. 2018 09; 22(3):225-232.
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Ruaud L, Rice GI, Cabrol C, Piard J, Rodero M, van Eyk L, Boucher-Brischoux E, de Noordhout AM, Maré R, Scalais E, Pauly F, Debray FG, Dobyns W, Uggenti C, Park JW, Hur S, Livingston JH, Crow YJ, Van Maldergem L. Autosomal-dominant early-onset spastic paraparesis with brain calcification due to IFIH1 gain-of-function. Hum Mutat. 2018 08; 39(8):1076-1080.
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Fassio A, Esposito A, Kato M, Saitsu H, Mei D, Marini C, Conti V, Nakashima M, Okamoto N, Olmez Turker A, Albuz B, Semerci Gündüz CN, Yanagihara K, Belmonte E, Maragliano L, Ramsey K, Balak C, Siniard A, Narayanan V. De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy. Brain. 2018 06 01; 141(6):1703-1718.
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Khan R, Koppe S. Modern Management of Acute Liver Failure. Gastroenterol Clin North Am. 2018 Jun; 47(2):313-326.
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Syrbe S, Harms FL, Parrini E, Montomoli M, Mütze U, Helbig KL, Polster T, Albrecht B, Bernbeck U, van Binsbergen E, Biskup S, Burglen L, Denecke J, Heron B, Heyne HO, Hoffmann GF, Hornemann F, Matsushige T, Matsuura R, Kato M, Korenke GC, Kuechler A, Lämmer C, Merkenschlager A, Mignot C, Ruf S, Nakashima M, Saitsu H, Stamberger H, Pisano T, Tohyama J, Weckhuysen S, Werckx W, Wickert J, Mari F, Verbeek NE, Møller RS, Koeleman B, Matsumoto N, Dobyns WB, Battaglia D, Lemke JR, Kutsche K, Guerrini R. Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy. Brain. 2017 Sep 01; 140(9):2322-2336.
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