cholestanol has been researched along with Adiadochokinesis in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cai, YH; Chen, C; Ding, ZT; Gong, LY; Sun, YM; Wang, J; Wu, H; Wu, JJ; Zhang, Y | 1 |
| Hur, KY; Jin, SM; Ki, CS; Kim, HK; Kim, JH; Kim, KW; Kim, MY; Kim, SW; Park, HD; Suh, S | 1 |
| Clemen, CS; Dodel, R; Klockgether, T; Lütjohann, D; Spottke, EA; Urbach, H; von Bergmann, K | 1 |
| Björkhem, I; Eggertsen, G; Fujiyama, J; Kim, KS; Kubota, S; Kuriyama, M; Seyama, Y | 1 |
4 other study(ies) available for cholestanol and Adiadochokinesis
| Article | Year |
|---|---|
Clinical and molecular genetic features of cerebrotendinous xanthomatosis patients in Chinese families.
Topics: Adult; Age of Onset; Asian People; Cerebellar Ataxia; Cholestanetriol 26-Monooxygenase; Cholestanol; Cognition Disorders; Disease Progression; Female; Genetic Testing; Humans; Male; Middle Aged; Mutation; Paraparesis, Spastic; Pedigree; Polymerase Chain Reaction; Xanthomatosis; Xanthomatosis, Cerebrotendinous | 2017 |
Three siblings with Cerebrotendinous Xanthomatosis: a novel mutation in the CYP27A1 gene.
Topics: Adult; Amino Acid Substitution; Cataract; Cerebellar Ataxia; Chenodeoxycholic Acid; Cholestanetriol 26-Monooxygenase; Cholestanol; Female; Humans; INDEL Mutation; Intellectual Disability; Male; Middle Aged; Pedigree; Peripheral Nervous System Diseases; Sequence Analysis, DNA; Siblings; Xanthomatosis, Cerebrotendinous | 2012 |
Cerebrotendinous xanthomatosis: a treatable ataxia.
Topics: Adult; Cerebellar Ataxia; Cerebellum; Chenodeoxycholic Acid; Cholestanol; Cholesterol; Disease Progression; Electroencephalography; Humans; Magnetic Resonance Imaging; Male; Paraparesis, Spastic; Peripheral Nervous System Diseases; Simvastatin; Treatment Outcome; Xanthomatosis, Cerebrotendinous | 2005 |
Identification of new mutations in sterol 27-hydroxylase gene in Japanese patients with cerebrotendinous xanthomatosis (CTX).
Topics: Adult; Arteriosclerosis; Base Sequence; Cerebellar Ataxia; Cholestanetriol 26-Monooxygenase; Cholestanol; Cholesterol; Cytochrome P-450 Enzyme System; Dementia; Fibroblasts; Humans; Japan; Molecular Sequence Data; Mutation; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Steroid Hydroxylases; Xanthomatosis | 1994 |