Diurnal Variation of Urinary Fabry Disease Biomarkers during Enzyme Replacement Therapy Cycles.
Adult
Biomarkers
/ urine
Case-Control Studies
Circadian Rhythm
Drug Administration Schedule
Drug Chronotherapy
Enzyme Replacement Therapy
Fabry Disease
/ drug therapy
Female
Glycolipids
/ urine
Humans
Infusions, Intravenous
Male
Sphingolipids
/ urine
Treatment Outcome
Trihexosylceramides
/ urine
alpha-Galactosidase
/ administration & dosage
Fabry disease
diurnal variation
globotriaosylceramide
globotriaosylsphingosine
glycosphingolipids
mass spectrometry
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
25 Aug 2020
25 Aug 2020
Historique:
received:
24
07
2020
revised:
19
08
2020
accepted:
21
08
2020
entrez:
29
8
2020
pubmed:
29
8
2020
medline:
23
2
2021
Statut:
epublish
Résumé
Fabry disease is an X-linked lysosomal storage disorder caused by mutations in the
Identifiants
pubmed: 32854306
pii: ijms21176114
doi: 10.3390/ijms21176114
pmc: PMC7503492
pii:
doi:
Substances chimiques
Biomarkers
0
Glycolipids
0
Sphingolipids
0
Trihexosylceramides
0
globotriaosyl lysosphingolipid
126550-86-5
globotriaosylceramide
71965-57-6
alpha-Galactosidase
EC 3.2.1.22
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Références
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