"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 characteristic symptom complex.
Descriptor ID |
D013577
|
MeSH Number(s) |
C23.550.288.500
|
Concept/Terms |
Syndrome- Syndrome
- Syndromes
- Symptom Cluster
- Cluster, Symptom
- Clusters, Symptom
- Symptom Clusters
|
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 |
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1995 | 0 | 1 | 1 |
1996 | 0 | 1 | 1 |
1997 | 0 | 2 | 2 |
1998 | 0 | 1 | 1 |
2001 | 0 | 3 | 3 |
2002 | 0 | 16 | 16 |
2003 | 0 | 15 | 15 |
2004 | 0 | 8 | 8 |
2005 | 0 | 18 | 18 |
2006 | 0 | 19 | 19 |
2007 | 1 | 24 | 25 |
2008 | 0 | 22 | 22 |
2009 | 0 | 14 | 14 |
2010 | 0 | 15 | 15 |
2011 | 0 | 10 | 10 |
2012 | 0 | 9 | 9 |
2013 | 0 | 7 | 7 |
2014 | 0 | 10 | 10 |
2015 | 0 | 8 | 8 |
2016 | 0 | 9 | 9 |
2017 | 0 | 5 | 5 |
2018 | 0 | 2 | 2 |
2019 | 0 | 5 | 5 |
2020 | 0 | 8 | 8 |
2021 | 0 | 7 | 7 |
2022 | 0 | 8 | 8 |
2023 | 0 | 1 | 1 |
2024 | 0 | 4 | 4 |
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Below are the most recent publications written about "Syndrome" by people in Profiles.
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Esmaeilzadeh E, Biglari S, Mosallaei M, Khorshid HRK, Vahidnezhad H, Tabatabaiefar MA. A Novel Homozygote Pathogenic Variant in the DIAPH1 Gene Associated With Seizures, Cortical Blindness, and Microcephaly Syndrome (SCBMS): Report of a Family and Literature Review. Mol Genet Genomic Med. 2024 Nov; 12(11):e70031.
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Burgei J, Alsheimer KM, Lantry J, Hehn B. Mediastinal lymphadenopathy due to VEXAS syndrome. BMJ Case Rep. 2024 Aug 08; 17(8).
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Connolly M, Hawkshaw MJ, Sataloff RT. Havana syndrome: Overview for otolaryngologists. Am J Otolaryngol. 2024 Jul-Aug; 45(4):104332.
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Nahas SJ. Cranial Neuralgias. Continuum (Minneap Minn). 2024 Apr 01; 30(2):473-487.
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Aid M, Stephenson KE, Collier AY, Nkolola JP, Michael JV, McKenzie SE, Barouch DH. Activation of coagulation and proinflammatory pathways in thrombosis with thrombocytopenia syndrome and following COVID-19 vaccination. Nat Commun. 2023 Oct 23; 14(1):6703.
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Shah VN, Java AP, Plestis KA. Successful management of iliofemoral and visceral malperfusion syndrome in acute type A aortic dissection with endovascular revascularization followed by delayed proximal aortic repair. J Card Surg. 2022 Dec; 37(12):5509-5512.
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Berberian JG. Hereditary Syndromes of Sudden Cardiac Death. Emerg Med Clin North Am. 2022 Nov; 40(4):651-662.
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Yoshida Y, Zeni JA, Zhu Y, Rhyne RL. Concurrent Validity Between Potential Screening Tests for Early Mobility Decline in Independent Community Dwellers. J Geriatr Phys Ther. 2022 Oct-Dec 01; 45(4):E161-E168.
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Dotan G, Jain S, Vagge A, Nelson LB. Diagnosis and Management of Strabismus Syndromes. J Pediatr Ophthalmol Strabismus. 2022 Jul-Aug; 59(4):210-212.
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Han JH, Ryan G, Guy A, Liu L, Quinodoz M, Helbling I, Lai-Cheong JE, Barwell J, Folcher M, McGrath JA, Moss C, Rivolta C. Mutations in the ribosome biogenesis factor gene LTV1 are linked to LIPHAK syndrome, a novel poikiloderma-like disorder. Hum Mol Genet. 2022 06 22; 31(12):1970-1978.