melatonin has been researched along with Fabry Disease in 2 studies
Fabry Disease: An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders.
Excerpt | Relevance | Reference |
---|---|---|
"Fabry disease is a progressive disease characterized by an enzymatic deficiency of acid alpha-galactosidase and glycosphingolipids storage within the lysosomes." | 5.51 | Rhythmic changes in Fabry disease: Inversion and non-oscillatory pattern in 6-sulfatoxymelatonin daily profile. ( Amaral, FGD; Cipolla-Neto, J; D'Almeida, V; Vallim, JRDS, 2019) |
"Fabry disease is a progressive disease characterized by an enzymatic deficiency of acid alpha-galactosidase and glycosphingolipids storage within the lysosomes." | 1.51 | Rhythmic changes in Fabry disease: Inversion and non-oscillatory pattern in 6-sulfatoxymelatonin daily profile. ( Amaral, FGD; Cipolla-Neto, J; D'Almeida, V; Vallim, JRDS, 2019) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 1 (50.00) | 2.80 |
Authors | Studies |
---|---|
Vallim, JRDS | 2 |
do Amaral, FG | 1 |
D'Almeida, V | 2 |
Amaral, FGD | 1 |
Cipolla-Neto, J | 1 |
2 other studies available for melatonin and Fabry Disease
Article | Year |
---|---|
Sleep parameters assessed by actigraphy in Fabry's disease patients: a proof-of-concept.
Topics: Actigraphy; Adult; Case-Control Studies; Cross-Sectional Studies; Fabry Disease; Female; Humans; Mal | 2020 |
Rhythmic changes in Fabry disease: Inversion and non-oscillatory pattern in 6-sulfatoxymelatonin daily profile.
Topics: Adolescent; Adult; Case-Control Studies; Circadian Rhythm; Fabry Disease; Female; Humans; Male; Mela | 2019 |