"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.
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 Harvard Catalyst Profiles by year, and whether "Syndrome" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1994 | 0 | 29 | 29 |
1995 | 0 | 34 | 34 |
1996 | 0 | 37 | 37 |
1997 | 0 | 37 | 37 |
1998 | 1 | 53 | 54 |
1999 | 0 | 47 | 47 |
2000 | 0 | 66 | 66 |
2001 | 0 | 71 | 71 |
2002 | 0 | 79 | 79 |
2003 | 0 | 87 | 87 |
2004 | 1 | 71 | 72 |
2005 | 2 | 94 | 96 |
2006 | 0 | 99 | 99 |
2007 | 0 | 85 | 85 |
2008 | 0 | 70 | 70 |
2009 | 0 | 69 | 69 |
2010 | 0 | 62 | 62 |
2011 | 0 | 45 | 45 |
2012 | 0 | 47 | 47 |
2013 | 0 | 44 | 44 |
2014 | 0 | 39 | 39 |
2015 | 0 | 51 | 51 |
2016 | 0 | 45 | 45 |
2017 | 0 | 42 | 42 |
2018 | 0 | 46 | 46 |
2019 | 1 | 41 | 42 |
2020 | 1 | 69 | 70 |
2021 | 0 | 62 | 62 |
2022 | 0 | 70 | 70 |
2023 | 0 | 55 | 55 |
2024 | 0 | 1 | 1 |
Below are the most recent publications written about "Syndrome" by people in Profiles.
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Stability and consistency of symptom clusters in younger versus older patients receiving chemotherapy. BMC Geriatr. 2024 Feb 16; 24(1):164.
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A prospective cohort study of a new electrosurgical unit for preventing colorectal post-endoscopic submucosal dissection coagulation syndrome. J Gastroenterol Hepatol. 2024 Mar; 39(3):473-479.
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Delays to care in infantile epileptic spasms syndrome: Racial and ethnic inequities. Epilepsia. 2024 Jan; 65(1):107-114.
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Sunflower Syndrome: A Survey of Provider Awareness and Management Preferences. Pediatr Neurol. 2024 Mar; 152:177-183.
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Clinical and molecular features of four families with CLDN10-related HELIX syndrome. Eur J Med Genet. 2023 Dec; 66(12):104886.
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Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndrome. Am J Hum Genet. 2023 Dec 07; 110(12):2112-2119.
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Gene therapy for congenital marrow failure syndromes - no longer grasping at straws? Haematologica. 2023 11 01; 108(11):2880-2882.
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Activation of coagulation and proinflammatory pathways in thrombosis with thrombocytopenia syndrome and following COVID-19 vaccination. Nat Commun. 2023 10 23; 14(1):6703.
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Complement. Arthritis Rheumatol. 2024 01; 76(1):1-8.
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Automating risk stratification for geriatric syndromes in the emergency department. J Am Geriatr Soc. 2024 01; 72(1):258-267.