Page last updated: 2024-08-23

miglustat and Fabry Disease

miglustat has been researched along with Fabry Disease in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (83.33)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Andreotti, G; Cubellis, MV; Monticelli, M1
Etou, Y1
Brady, RO1
Alp, NJ; Butters, TD; Channon, KM; Clarke, K; Dwek, RA; Heare, T; Kulkarni, AB; Platt, FM; Priestman, DA; Qasba, P1
Abe, A; Arend, LJ; Brady, RO; Lee, L; Lingwood, C; Shayman, JA1
Abe, A; Brady, RO; Gregory, S; Killen, PD; Kulkarni, A; Lee, L; Shayman, JA1

Reviews

2 review(s) available for miglustat and Fabry Disease

ArticleYear
[Recent therapeutics for Fabry disease].
    Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine, 2009, Apr-10, Volume: 98, Issue:4

    Topics: 1-Deoxynojirimycin; alpha-Galactosidase; Cell- and Tissue-Based Therapy; Fabry Disease; Genetic Therapy; Glucosamine; Humans; Isoenzymes; Mass Screening; Trihexosylceramides

2009
Emerging strategies for the treatment of hereditary metabolic storage disorders.
    Rejuvenation research, 2006,Summer, Volume: 9, Issue:2

    Topics: 1-Deoxynojirimycin; Bone Marrow Transplantation; Enzyme Inhibitors; Fabry Disease; Gangliosidosis, GM1; Gaucher Disease; Genetic Therapy; Humans; Imino Sugars; Piperidines

2006

Other Studies

4 other study(ies) available for miglustat and Fabry Disease

ArticleYear
Looking for protein stabilizing drugs with thermal shift assay.
    Drug testing and analysis, 2015, Volume: 7, Issue:9

    Topics: 1-Deoxynojirimycin; alpha-Galactosidase; Drug Evaluation, Preclinical; Enzyme Stability; Fabry Disease; Glycogen Storage Disease Type II; High-Throughput Screening Assays; Humans; Temperature

2015
Severe endothelial dysfunction in the aorta of a mouse model of Fabry disease; partial prevention by N-butyldeoxynojirimycin treatment.
    Journal of inherited metabolic disease, 2007, Volume: 30, Issue:1

    Topics: 1-Deoxynojirimycin; alpha-Galactosidase; Animals; Aorta; Disease Models, Animal; Enzyme Inhibitors; Fabry Disease; Female; Humans; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Microscopy, Electron; Phenotype

2007
Glycosphingolipid depletion in fabry disease lymphoblasts with potent inhibitors of glucosylceramide synthase.
    Kidney international, 2000, Volume: 57, Issue:2

    Topics: 1-Deoxynojirimycin; alpha-Galactosidase; B-Lymphocytes; Bacterial Toxins; Cell Line, Transformed; Dose-Response Relationship, Drug; Enzyme Inhibitors; Fabry Disease; Fluorescein-5-isothiocyanate; Fluorescent Dyes; Genetic Vectors; Glucosyltransferases; Glycosphingolipids; Herpesvirus 4, Human; Humans; Neutral Glycosphingolipids; Propanolamines; Pyrrolidines; Shiga Toxin 1; Trihexosylceramides

2000
Reduction of globotriaosylceramide in Fabry disease mice by substrate deprivation.
    The Journal of clinical investigation, 2000, Volume: 105, Issue:11

    Topics: 1-Deoxynojirimycin; Animals; Dose-Response Relationship, Drug; Fabry Disease; Kidney; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Propanolamines; Pyrrolidines; Trihexosylceramides

2000