"Hyperammonemia" 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.
Elevated level of AMMONIA in the blood. It is a sign of defective CATABOLISM of AMINO ACIDS or ammonia to UREA.
Descriptor ID |
D022124
|
MeSH Number(s) |
C23.550.421
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hyperammonemia".
Below are MeSH descriptors whose meaning is more specific than "Hyperammonemia".
This graph shows the total number of publications written about "Hyperammonemia" by people in this website by year, and whether "Hyperammonemia" 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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2001 | 0 | 1 | 1 |
2002 | 0 | 1 | 1 |
2003 | 0 | 1 | 1 |
2006 | 3 | 0 | 3 |
2008 | 1 | 0 | 1 |
2010 | 1 | 2 | 3 |
2011 | 2 | 1 | 3 |
2012 | 1 | 2 | 3 |
2013 | 1 | 0 | 1 |
2014 | 2 | 2 | 4 |
2015 | 2 | 2 | 4 |
2017 | 1 | 0 | 1 |
2019 | 1 | 2 | 3 |
2020 | 3 | 1 | 4 |
2021 | 1 | 1 | 2 |
2022 | 2 | 0 | 2 |
2023 | 1 | 0 | 1 |
2024 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hyperammonemia" by people in Profiles.
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Unraveling the Link: Seizure Characteristics and Ammonia Levels in Urea Cycle Disorder During Hyperammonemic Crises. Pediatr Neurol. 2024 Oct; 159:48-55.
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Health-related quality of life in a systematically assessed cohort of children and adults with urea cycle disorders. Mol Genet Metab. 2023 11; 140(3):107696.
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Predicting the disease severity in male individuals with ornithine transcarbamylase deficiency. Ann Clin Transl Neurol. 2022 11; 9(11):1715-1726.
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Multisite Retrospective Review of Outcomes in Renal Replacement Therapy for Neonates with Inborn Errors of Metabolism. J Pediatr. 2022 07; 246:116-122.e1.
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Perceptions and use of phenylbutyrate metabolite testing in urea cycle disorders: Results of a clinician survey and analysis of a centralized testing database. Mol Genet Metab. 2022 01; 135(1):35-41.
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Biomarkers for liver disease in urea cycle disorders. Mol Genet Metab. 2021 06; 133(2):148-156.
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Severity-adjusted evaluation of newborn screening on the metabolic disease course in individuals with cytosolic urea cycle disorders. Mol Genet Metab. 2020 12; 131(4):390-397.
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Sunitinib-associated hyperammonemic encephalopathy. Am J Emerg Med. 2021 08; 46:282-283.
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Survival and Neurologic Recovery After Prompt Diagnosis and Aggressive Management of Severe Idiopathic Hyperammonemic Encephalopathy in a Patient with Acute Myeloid Leukemia. J Pediatr Hematol Oncol. 2020 08; 42(6):e452-e455.
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Hyperammonemia From Ureaplasma Infection in an Immunocompromised Child. J Pediatr Hematol Oncol. 2020 03; 42(2):e114-e116.