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conduritol epoxide and Autosomal Dominant Juvenile Parkinson Disease

conduritol epoxide has been researched along with Autosomal Dominant Juvenile Parkinson Disease in 2 studies

conduritol epoxide: conduritol C epoxide refers to the (epi & neo)-isomers; structure
conduritol epoxide : An epoxide resulting from the epoxidation of the double bond of a conduritol.

Research Excerpts

ExcerptRelevanceReference
"Gaucher disease is an autosomal recessive disease, caused by a lack or functional deficiency of the lysosomal enzyme, glucocerebrosidase (GCase)."1.42Glucocerebrosidase deficiency and mitochondrial impairment in experimental Parkinson disease. ( Alvarez-Fischer, D; Andreas, H; Hirsch, EC; Höglinger, GU; Höllerhage, M; Lu, L; Noelker, C; Oertel, WH; Roscher, R; Sturn, A; Vulinovic, F, 2015)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Mus, L1
Siani, F1
Giuliano, C1
Ghezzi, C1
Cerri, S1
Blandini, F1
Noelker, C1
Lu, L1
Höllerhage, M1
Vulinovic, F1
Sturn, A1
Roscher, R1
Höglinger, GU1
Hirsch, EC1
Oertel, WH1
Alvarez-Fischer, D1
Andreas, H1

Other Studies

2 other studies available for conduritol epoxide and Autosomal Dominant Juvenile Parkinson Disease

ArticleYear
Development and biochemical characterization of a mouse model of Parkinson's disease bearing defective glucocerebrosidase activity.
    Neurobiology of disease, 2019, Volume: 124

    Topics: Animals; Disease Models, Animal; Enzyme Inhibitors; Glucosylceramidase; Inositol; Male; Mice; Mice,

2019
Glucocerebrosidase deficiency and mitochondrial impairment in experimental Parkinson disease.
    Journal of the neurological sciences, 2015, Sep-15, Volume: 356, Issue:1-2

    Topics: 1-Deoxynojirimycin; 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; Animals; Brain; Cell Count; Cells,

2015