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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2018 | 2 | 0 | 2 |
| 2019 | 3 | 1 | 4 |
| 2020 | 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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Challenges in Chronic Genetic Disorders: Lessons From the COVID-19 Pandemic. Indian Pediatr. 2021 Apr 15; 58(4):391-392.
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Invisible burden of COVID-19: enzyme replacement therapy disruptions. J Pediatr Endocrinol Metab. 2021 May 26; 34(5):539-545.
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Impact of COVID-19 related healthcare crisis on treatments for patients with lysosomal storage disorders, the first Italian experience. Mol Genet Metab. 2020 07; 130(3):170-171.
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Plasma and dried blood spot lysosphingolipids for the diagnosis of different sphingolipidoses: a comparative study. Clin Chem Lab Med. 2019 Nov 26; 57(12):1863-1874.
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Liver Transplantation for Lysosomal Storage Disorders: A Novel Option to Pick. Liver Transpl. 2019 08; 25(8):1140-1141.
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Molecular Pathways and Respiratory Involvement in Lysosomal Storage Diseases. Int J Mol Sci. 2019 Jan 15; 20(2).
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Ophthalmic manifestations of Gaucher disease: the most common lysosomal storage disorder. Br J Ophthalmol. 2019 03; 103(3):315-326.
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Identifying genes in Parkinson disease: state of the art. Med J Aust. 2018 05 21; 208(9):381-382.
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Spastic paraparesis caused by X-linked adrenoleukodystrophy mimicking vacuolar myelopathy in a human immunodeficiency virus patient: A case report. Medicine (Baltimore). 2018 May; 97(20):e10756.