Fatal Outcome
"Fatal Outcome" 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.
Death resulting from the presence of a disease in an individual, as shown by a single case report or a limited number of patients. This should be differentiated from DEATH, the physiological cessation of life and from MORTALITY, an epidemiological or statistical concept.
Descriptor ID |
D017809
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MeSH Number(s) |
E05.318.308.985.550.325 L01.280.975.550.325 N01.224.935.698.201 N06.850.505.400.975.550.325 N06.850.520.308.985.550.325
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Concept/Terms |
Fatal Outcome- Fatal Outcome
- Fatal Outcomes
- Outcome, Fatal
- Outcomes, Fatal
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Below are MeSH descriptors whose meaning is more general than "Fatal Outcome".
Below are MeSH descriptors whose meaning is more specific than "Fatal Outcome".
This graph shows the total number of publications written about "Fatal Outcome" by people in this website by year, and whether "Fatal Outcome" 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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1994 | 0 | 4 | 4 | 1995 | 0 | 2 | 2 | 1996 | 0 | 3 | 3 | 1997 | 0 | 2 | 2 | 1998 | 0 | 5 | 5 | 1999 | 0 | 2 | 2 | 2000 | 0 | 2 | 2 | 2001 | 0 | 3 | 3 | 2002 | 0 | 4 | 4 | 2003 | 0 | 7 | 7 | 2004 | 0 | 6 | 6 | 2005 | 0 | 5 | 5 | 2006 | 0 | 7 | 7 | 2007 | 0 | 4 | 4 | 2008 | 0 | 12 | 12 | 2009 | 0 | 6 | 6 | 2010 | 0 | 2 | 2 | 2011 | 0 | 7 | 7 | 2012 | 0 | 5 | 5 | 2013 | 0 | 4 | 4 | 2015 | 0 | 9 | 9 | 2016 | 0 | 6 | 6 | 2017 | 0 | 4 | 4 | 2018 | 0 | 2 | 2 | 2019 | 0 | 3 | 3 | 2020 | 0 | 3 | 3 |
To return to the timeline, click here.
Below are the most recent publications written about "Fatal Outcome" by people in Profiles.
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Bitterman Y, Hubara E, Hadash A, Ben-Ari J, Annich G, Eytan D. Methylene Blue Administration for Distributive Shock States in Critically Ill Children. Isr Med Assoc J. 2020 Jul; 22(7):404-408.
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Gauquelin L, Hawkins C, Tam EWY, Miller SP, Yoon G. Pearls & Oy-sters: Fatal brain edema is a rare complication of severe CACNA1A-related disorder. Neurology. 2020 04 07; 94(14):631-634.
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Torralba-Raga L, Tesi B, Chiang SCC, Schlums H, Nordenskjöld M, Horne A, Henter JI, Meeths M, Abdelhaleem M, Weitzman S, Bryceson Y. Diagnostic challenges for a novel SH2D1A mutation associated with X-linked lymphoproliferative disease. Pediatr Blood Cancer. 2020 04; 67(4):e28184.
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Oshrine B, Grana N, Moore C, Nguyen J, Crenshaw M, Edwards M, Sudhaman S, Forster VJ, Tabori U. B-cell acute lymphoblastic leukemia with high mutation burden presenting in a child with constitutional mismatch repair deficiency. Blood Adv. 2019 06 25; 3(12):1795-1798.
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D'Arcy CE, Bitnun A, Coulthart MB, D'Amour R, Friedman J, Knox JD, Rapoport A, Carter S, Widjaja E, Hazrati LN, Jansen GH. Sporadic Creutzfeldt-Jakob Disease in a Young Girl With Unusually Long Survival. J Neuropathol Exp Neurol. 2019 04 01; 78(4):373-378.
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Gelder CL, Hawkins C, Zapotocky M, Dirks P, Bartels U, Bouffet E. Diffuse intrinsic pontine glioma ventricular peritoneal shunt metastasis: a case report and literature review. Childs Nerv Syst. 2019 05; 35(5):861-864.
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Van Ommeren RH, Gao AF, Blaser SI, Chitayat DA, Hazrati LN. BRAT1 Mutation: The First Reported Case of Chinese Origin and Review of the Literature. J Neuropathol Exp Neurol. 2018 12 01; 77(12):1071-1078.
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Ho SSC, Nashid N, Waters VJ, LiPuma JJ, Zlosnik JEA, Otley A, Somers GR, Kamath BM, Yau YCW. Burkholderia multivorans septicemia in a pediatric liver transplant patient. Am J Transplant. 2019 03; 19(3):933-938.
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Goyal A, Cajigas I, Ibrahim GM, Brathwaite CD, Khatib Z, Niazi T, Bhatia S, Ragheb J. Surgical Treatment of Intramedullary Spinal Metastasis in Medulloblastoma: Case Report and Review of the Literature. World Neurosurg. 2018 Oct; 118:42-46.
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Ejaz R, Lionel AC, Blaser S, Walker S, Scherer SW, Babul-Hirji R, Marshall CR, Stavropoulos DJ, Chitayat D. De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delay. . 2017 Oct; 173(10):2725-2730.
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