"alpha-Galactosidase" 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.
An enzyme that catalyzes the hydrolysis of terminal, non-reducing alpha-D-galactose residues in alpha-galactosides including galactose oligosaccharides, galactomannans, and galactolipids.
| Descriptor ID |
D000519
|
| MeSH Number(s) |
D08.811.277.450.410.050
|
| Concept/Terms |
alpha-Galactosidase- alpha-Galactosidase
- alpha Galactosidase
- alpha-Galactosidases
- alpha Galactosidases
- Melibiase
- alpha-Galactosidase A
- alpha Galactosidase A
|
Below are MeSH descriptors whose meaning is more general than "alpha-Galactosidase".
Below are MeSH descriptors whose meaning is more specific than "alpha-Galactosidase".
This graph shows the total number of publications written about "alpha-Galactosidase" by people in this website by year, and whether "alpha-Galactosidase" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 0 | 1 |
| 1999 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2004 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2007 | 0 | 1 | 1 |
| 2008 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "alpha-Galactosidase" by people in Profiles.
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Fabry disease revisited: Management and treatment recommendations for adult patients. Mol Genet Metab. 2018 04; 123(4):416-427.
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Challenges in the Diagnosis of Anderson-Fabry Disease: A Deceptively Simple and Yet Complicated Genetic Disease. J Am Coll Cardiol. 2016 09 06; 68(10):1051-3.
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a-Galactosidase A knockout mice: progressive organ pathology resembles the type 2 later-onset phenotype of Fabry disease. Am J Pathol. 2015 Mar; 185(3):651-65.
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Characterization of Fabry disease in 352 pediatric patients in the Fabry Registry. Pediatr Res. 2008 Nov; 64(5):550-5.
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Females with Fabry disease frequently have major organ involvement: lessons from the Fabry Registry. Mol Genet Metab. 2008 Feb; 93(2):112-28.
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Fabry disease: guidelines for the evaluation and management of multi-organ system involvement. Genet Med. 2006 Sep; 8(9):539-48.
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Fabry disease: renal sonographic and magnetic resonance imaging findings in affected males and carrier females with the classic and cardiac variant phenotypes. J Comput Assist Tomogr. 2004 Mar-Apr; 28(2):158-68.
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Fabry disease: detection of undiagnosed hemodialysis patients and identification of a "renal variant" phenotype. Kidney Int. 2003 Sep; 64(3):801-7.
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Further associations of congenital heart disease and genetic syndromes: report of a case of tetralogy of Fallot and Fabry's disease. Pediatr Cardiol. 1999 May-Jun; 20(3):236-7.
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Sixty-nine kilobases of contiguous human genomic sequence containing the alpha-galactosidase A and Bruton's tyrosine kinase loci. Mamm Genome. 1995 May; 6(5):334-8.