Lysosomal Storage Diseases
"Lysosomal Storage Diseases" 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.
Inborn errors of metabolism characterized by defects in specific lysosomal hydrolases and resulting in intracellular accumulation of unmetabolized substrates.
| Descriptor ID |
D016464
|
| MeSH Number(s) |
C16.320.565.595 C18.452.648.595
|
| Concept/Terms |
Lysosomal Storage Diseases- Lysosomal Storage Diseases
- Disease, Lysosomal Storage
- Diseases, Lysosomal Storage
- Lysosomal Storage Disease
- Lysosomal Enzyme Disorders
- Disorder, Lysosomal Enzyme
- Disorders, Lysosomal Enzyme
- Enzyme Disorder, Lysosomal
- Enzyme Disorders, Lysosomal
- Lysosomal Enzyme Disorder
|
Below are MeSH descriptors whose meaning is more general than "Lysosomal Storage Diseases".
Below are MeSH descriptors whose meaning is more specific than "Lysosomal Storage Diseases".
This graph shows the total number of publications written about "Lysosomal Storage Diseases" by people in this website by year, and whether "Lysosomal Storage Diseases" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2012 | 0 | 1 | 1 |
| 2016 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Lysosomal Storage Diseases" by people in Profiles.
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An unexpected player in Gaucher disease: The multiple roles of complement in disease development. Semin Immunol. 2018 06; 37:30-42.
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PATIENT-REPORTED OUTCOMES IN RARE LYSOSOMAL STORAGE DISEASES: KEY INFORMANT INTERVIEWS AND A SYSTEMATIC REVIEW PROTOCOL. Int J Technol Assess Health Care. 2016 Jan; 32(6):393-399.
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Limited responsiveness related to the minimal important difference of patient-reported outcomes in rare diseases. J Clin Epidemiol. 2016 11; 79:10-21.
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Gaucher disease and other storage disorders. Hematology Am Soc Hematol Educ Program. 2012; 2012:13-8.
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Multi-system disorders of glycosphingolipid and ganglioside metabolism. J Lipid Res. 2010 Jul; 51(7):1643-75.
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Induction of the manganese superoxide dismutase gene by sphingomyelinase and ceramide. J Neurochem. 1999 Aug; 73(2):513-20.