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 characteristic symptom complex.
Descriptor ID |
D013577
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MeSH Number(s) |
C23.550.288.500
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Concept/Terms |
Syndrome- Syndrome
- Syndromes
- Symptom Cluster
- Cluster, Symptom
- Clusters, Symptom
- Symptom Clusters
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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 |
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1995 | 0 | 2 | 2 | 1996 | 0 | 3 | 3 | 1997 | 0 | 3 | 3 | 1998 | 0 | 5 | 5 | 1999 | 0 | 8 | 8 | 2000 | 0 | 6 | 6 | 2001 | 0 | 3 | 3 | 2002 | 0 | 4 | 4 | 2003 | 0 | 6 | 6 | 2004 | 0 | 9 | 9 | 2005 | 0 | 12 | 12 | 2006 | 0 | 16 | 16 | 2007 | 0 | 14 | 14 | 2008 | 0 | 9 | 9 | 2009 | 0 | 10 | 10 | 2010 | 0 | 8 | 8 | 2011 | 0 | 7 | 7 | 2012 | 0 | 5 | 5 | 2013 | 0 | 4 | 4 | 2014 | 0 | 6 | 6 | 2015 | 0 | 10 | 10 | 2016 | 0 | 8 | 8 | 2017 | 0 | 6 | 6 | 2018 | 0 | 9 | 9 | 2019 | 0 | 8 | 8 | 2020 | 0 | 7 | 7 | 2021 | 0 | 12 | 12 | 2022 | 0 | 10 | 10 | 2023 | 0 | 10 | 10 | 2024 | 0 | 9 | 9 |
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Below are the most recent publications written about "Syndrome" by people in Profiles.
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Sanders J, Conway AE, Kartha N, Kumar BP, Oppenheimer J, Verdi M, Anagnostou A, Abrams EM, Blatman KSH, Greenhawt M, Shaker MS. Cost-effectiveness of shared decision-making in determining challenge setting for nonsevere food protein-induced enterocolitis syndrome. Ann Allergy Asthma Immunol. 2025 Jun; 134(6):706-712.e2.
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Shaker M, Abrams EM, Greenhawt M, Joshi S, Lieberman J, Mustafa SS, Anagnostou A. Shared Decision-Making in Food Protein-Induced Enterocolitis Syndrome. J Allergy Clin Immunol Pract. 2025 Jun; 13(6):1310-1316.
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Mullen MP, Ivy DD, Varghese NP, Winant AJ, Cortes-Santiago N, Vargas SO, Porres D, Maschietto N, Critser PJ, Hirsch R, Avitabile CM, Hopper RK, Frank BS, Coleman RD, Agrawal PB, Madden JA, Roberts AE, Collins SL, Raj JU, Austin ED, Chung WK, Abman SH. SOX17-Associated Pulmonary Hypertension in Children: A Distinct Developmental and Clinical Syndrome. J Pediatr. 2025 Mar; 278:114422.
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Whipple MO, Craswell J. Mid-aortic syndrome presenting in adulthood: A case report and review of the literature. J Vasc Nurs. 2024 Sep; 42(3):213-215.
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Huang Y, Jay KL, Yen-Wen Huang A, Wan J, Jangam SV, Chorin O, Rothschild A, Barel O, Mariani M, Iascone M, Xue H, Huang J, Mignot C, Keren B, Saillour V, Mah-Som AY, Sacharow S, Rajabi F, Costin C, Yamamoto S, Kanca O, Bellen HJ, Rosenfeld JA, Palmer CGS, Nelson SF, Wangler MF, Martinez-Agosto JA. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly. Genet Med. 2024 Nov; 26(11):101218.
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Shanker AI, Li BUK, Kramer RE. Cannabinoid hyperemesis syndrome co-occurring with superior mesenteric artery syndrome in adolescents. J Pediatr Gastroenterol Nutr. 2024 Sep; 79(3):495-500.
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Chen Y, Dawes R, Kim HC, Ljungdahl A, Stenton SL, Walker S, Lord J, Lemire G, Martin-Geary AC, Ganesh VS, Ma J, Ellingford JM, Delage E, D'Souza EN, Dong S, Adams DR, Allan K, Bakshi M, Baldwin EE, Berger SI, Bernstein JA, Bhatnagar I, Blair E, Brown NJ, Burrage LC, Chapman K, Coman DJ, Compton AG, Cunningham CA, D'Souza P, Danecek P, D?lot EC, Dias KR, Elias ER, Elmslie F, Evans CA, Ewans L, Ezell K, Fraser JL, Gallacher L, Genetti CA, Goriely A, Grant CL, Haack T, Higgs JE, Hinch AG, Hurles ME, Kuechler A, Lachlan KL, Lalani SR, Lecoquierre F, Leit?o E, Fevre AL, Leventer RJ, Liebelt JE, Lindsay S, Lockhart PJ, Ma AS, Macnamara EF, Mansour S, Maurer TM, Mendez HR, Metcalfe K, Montgomery SB, Moosajee M, Nassogne MC, Neumann S, O'Donoghue M, O'Leary M, Palmer EE, Pattani N, Phillips J, Pitsava G, Pysar R, Rehm HL, Reuter CM, Revencu N, Riess A, Rius R, Rodan L, Roscioli T, Rosenfeld JA, Sachdev R, Shaw-Smith CJ, Simons C, Sisodiya SM, Snell P, St Clair L, Stark Z, Stewart HS, Tan TY, Tan NB, Temple SEL, Thorburn DR, Tifft CJ, Uebergang E, VanNoy GE, Vasudevan P, Vilain E, Viskochil DH, Wedd L, Wheeler MT, White SM, Wojcik M, Wolfe LA, Wolfenson Z, Wright CF, Xiao C, Zocche D, Rubenstein JL, Markenscoff-Papadimitriou E, Fica SM, Baralle D, Depienne C, MacArthur DG, Howson JMM, Sanders SJ, O'Donnell-Luria A, Whiffin N. De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature. 2024 Aug; 632(8026):832-840.
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Mehta JS, Pahys JM, Saad A, Sponseller P, Andras L, Marks D, Poon S, Klineberg E, White KK, Helenius I, Welborn M, Redding G. Paediatric syndromic scoliosis: proceedings of the half-day course at the 57th annual meeting of the Scoliosis Research Society. Spine Deform. 2024 May; 12(3):523-543.
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Smalling S, Roberts J, Hendrick K, Gray M, Wyrwa JM. Vestibular Testing and Impairments in Postoperative Pediatric Cerebellar Mutism Syndrome: A Case Series. Pediatr Neurol. 2024 May; 154:15-19.
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Szakszon K, Lourenco CM, Callewaert BL, Genevi?ve D, Rouxel F, Morin D, Denomm?-Pichon AS, Vitobello A, Patterson WG, Louie R, Pinto E Vairo F, Klee E, Kaiwar C, Gavrilova RH, Agre KE, Jacquemont S, Khadij? J, Giltay J, van Gassen K, Mero G, Gerkes E, Van Bon BW, Rinne T, Pfundt R, Brunner HG, Caluseriu O, Grasshoff U, Kehrer M, Haack TB, Khelifa MM, Bergmann AK, Cueto-Gonz?lez AM, Martorell AC, Ramachandrappa S, Sawyer LB, Fasel P, Braun D, Isis A, Superti-Furga A, McNiven V, Chitayat D, Ahmed SA, Brennenstuhl H, Schwaibolf EM, Battisti G, Parmentier B, Stevens SJC. Further delineation of the rare GDACCF (global developmental delay, absent or hypoplastic corpus callosum, dysmorphic facies syndrome): genotype and phenotype of 22 patients with ZNF148 mutations. J Med Genet. 2024 01 19; 61(2):132-141.
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