 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 | 9 | 9 | | 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 | 9 | 9 | | 2000 | 0 | 8 | 8 | | 2001 | 0 | 5 | 5 | | 2002 | 0 | 16 | 16 | | 2003 | 0 | 19 | 19 | | 2004 | 0 | 18 | 18 | | 2005 | 0 | 14 | 14 | | 2006 | 0 | 12 | 12 | | 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 | 7 | 7 | | 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Syndrome" by people in Profiles.
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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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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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Piché J, Gosset N, Legault LM, Pacis A, Oneglia A, Caron M, Chetaille P, Barreiro L, Liu D, Qi X, Nattel S, Leclerc S, Breton-Larrivée M. Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-ß Signaling and Epigenomics. Cell Mol Gastroenterol Hepatol. 2019; 7(2):411-431.
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Bianco AC, Kim BS. Pathophysiological relevance of deiodinase polymorphism. Curr Opin Endocrinol Diabetes Obes. 2018 10; 25(5):341-346.
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Pilch J, Koppolu AA, Walczak A, Murcia Pienkowski VA, Biernacka A, Skiba P, Machnik-Broncel J, Gasperowicz P, Kosinska J, Rydzanicz M, Emich-Widera E, Ploski R. Evidence for HNRNPH1 being another gene for Bain type syndromic mental retardation. Clin Genet. 2018 10; 94(3-4):381-385.
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Brock S, Stouffs K, Scalais E, D'Hooghe M, Keymolen K, Guerrini R, Dobyns WB, Di Donato N, Jansen AC. Tubulinopathies continued: refining the phenotypic spectrum associated with variants in TUBG1. Eur J Hum Genet. 2018 08; 26(8):1132-1142.
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Manning JC, Pinto NP, Rennick JE, Colville G, Curley MAQ. Conceptualizing Post Intensive Care Syndrome in Children-The PICS-p Framework. Pediatr Crit Care Med. 2018 04; 19(4):298-300.
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Lewis AH, Chugh A, Sobotka SA. Behavioral Outbursts in a Child with a Deletion Syndrome, Generalized Epilepsy, Global Developmental Delay, and Failure to Thrive. Pediatr Ann. 2018 Mar 01; 47(3):e130-e134.
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West AH, Churpek JE. Old and new tools in the clinical diagnosis of inherited bone marrow failure syndromes. Hematology Am Soc Hematol Educ Program. 2017 12 08; 2017(1):79-87.
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