 Syndrome
"Syndrome" 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 symptom complex of unknown etiology, that is characteristic of a particular abnormality.
| Descriptor ID |
D013577
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| MeSH Number(s) |
C23.550.288.500
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Syndrome".
This graph shows the total number of publications written about "Syndrome" by people in this website by year, and whether "Syndrome" 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 | 0 | 3 | 3 | | 1981 | 0 | 3 | 3 | | 1982 | 0 | 4 | 4 | | 1983 | 0 | 3 | 3 | | 1984 | 0 | 2 | 2 | | 1985 | 0 | 5 | 5 | | 1986 | 0 | 8 | 8 | | 1987 | 0 | 5 | 5 | | 1988 | 0 | 7 | 7 | | 1989 | 0 | 11 | 11 | | 1990 | 0 | 6 | 6 | | 1991 | 0 | 10 | 10 | | 1992 | 0 | 6 | 6 | | 1993 | 0 | 11 | 11 | | 1994 | 0 | 6 | 6 | | 1995 | 0 | 5 | 5 | | 1996 | 0 | 10 | 10 | | 1997 | 0 | 11 | 11 | | 1998 | 0 | 9 | 9 | | 1999 | 0 | 8 | 8 | | 2000 | 0 | 8 | 8 | | 2001 | 0 | 5 | 5 | | 2002 | 0 | 16 | 16 | | 2003 | 0 | 18 | 18 | | 2004 | 0 | 18 | 18 | | 2005 | 0 | 14 | 14 | | 2006 | 0 | 13 | 13 | | 2007 | 0 | 20 | 20 | | 2008 | 0 | 15 | 15 | | 2009 | 0 | 14 | 14 | | 2010 | 1 | 13 | 14 | | 2011 | 0 | 7 | 7 | | 2012 | 0 | 5 | 5 | | 2013 | 0 | 13 | 13 | | 2014 | 0 | 6 | 6 | | 2015 | 0 | 6 | 6 | | 2016 | 0 | 7 | 7 | | 2017 | 0 | 6 | 6 | | 2018 | 0 | 10 | 10 | | 2019 | 0 | 4 | 4 | | 2020 | 0 | 3 | 3 |
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Below are the most recent publications written about "Syndrome" by people in Profiles.
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Blumkin L, Leibovitz Z, Krajden-Haratz K, Arad A, Yosovich K, Gindes L, Zerem A, Ben-Sira L, Lev D, Nissenkorn A, Kidron D, Dobyns WB, Malinger G, Bahi-Buisson N, Leventer RJ, Lerman-Sagie T. Autosomal dominant TUBB3-related syndrome: Fetal, radiologic, clinical and morphological features. Eur J Paediatr Neurol. 2020 May; 26:46-60.
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Unlu G, Qi X, Gamazon ER, Melville DB, Patel N, Rushing AR, Hashem M, Al-Faifi A, Chen R, Li B, Cox NJ, Alkuraya FS, Knapik EW. Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies. Nat Med. 2020 01; 26(1):98-109.
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Mak CCY, Doherty D, Lin AE, Vegas N, Cho MT, Viot G, Dimartino C, Weisfeld-Adams JD, Lessel D, Joss S, Li C, Gonzaga-Jauregui C, Zarate YA, Ehmke N, Horn D, Troyer C, Kant SG, Lee Y, Ishak GE, Leung G, Barone Pritchard A, Yang S, Bend EG, Filippini F, Roadhouse C, Lebrun N, Mehaffey MG, Martin PM, Apple B, Millan F, Puk O, Hoffer MJV, Henderson LB, McGowan R, Wentzensen IM, Pei S, Zahir FR, Yu M, Gibson WT, Seman A, Steeves M, Murrell JR, Luettgen S, Francisco E, Strom TM, Amlie-Wolf L, Kaindl AM, Wilson WG, Halbach S, Basel-Salmon L, Lev-El N, Denecke J, Vissers LELM, Radtke K, Chelly J, Zackai E, Friedman JM, Bamshad MJ, Nickerson DA. MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain. 2020 01 01; 143(1):55-68.
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Burkardt DD, Tatton-Brown K, Dobyns W, Graham JM. Approach to overgrowth syndromes in the genome era. Am J Med Genet C Semin Med Genet. 2019 12; 181(4):483-490.
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Abdulkarim M, Karikari Y, Loomba RS, Anderson RH, Vricella L, El-Zein C. A Unique Case of Middle Aorta Syndrome With a "Corkscrew" Descending Aorta. World J Pediatr Congenit Heart Surg. 2019 11; 10(6):799-800.
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Dobyns WB, Mirzaa GM. Megalencephaly syndromes associated with mutations of core components of the PI3K-AKT-MTOR pathway: PIK3CA, PIK3R2, AKT3, and MTOR. Am J Med Genet C Semin Med Genet. 2019 12; 181(4):582-590.
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Kobashi K, Nitti V, Margolis E, Sand P, Siegel S, Khandwala S, Newman D, MacDiarmid SA, Kan F, Michaud E. A Prospective Study to Evaluate Efficacy Using the Nuro Percutaneous Tibial Neuromodulation System in Drug-Naïve Patients With Overactive Bladder Syndrome. Urology. 2019 Sep; 131:77-82.
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Erickson EA, Engel LS, Christenbury K, Weems L, Schwartz EG, Rusiecki JA. Environmental Heat Exposure and Heat-Related Symptoms in United States Coast Guard Deepwater Horizon Disaster Responders. Disaster Med Public Health Prep. 2019 06; 13(3):561-569.
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Smigiel R, Sherman DL, Rydzanicz M, Walczak A, Mikolajkow D, Krolak-Olejnik B, Kosinska J, Gasperowicz P, Biernacka A, Stawinski P, Marciniak M, Andrzejewski W, Boczar M, Krajewski P, Sasiadek MM, Brophy PJ, Ploski R. Homozygous mutation in the Neurofascin gene affecting the glial isoform of Neurofascin causes severe neurodevelopment disorder with hypotonia, amimia and areflexia. Hum Mol Genet. 2018 11 01; 27(21):3669-3674.
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Ginat DT. Imaging Findings in Syndromes with Temporal Bone Abnormalities. Neuroimaging Clin N Am. 2019 Feb; 29(1):117-128.
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