n-acetylaspartic acid has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 14 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 6 (42.86) | 29.6817 |
| 2010's | 8 (57.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bushara, KO; Deelchand, DK; Eberly, LE; Emir, UE; Gomez, CM; Hutter, D; Joers, JM; Lyu, T; Öz, G | 1 |
| Arsovic, A; Auburger, G; Bosman, LWJ; Canet-Pons, J; Chae, WH; De Zeeuw, CI; Gispert, S; Halbach, MV; Kaya, ZE; Meierhofer, D; Mittelbronn, M; Pilatus, U; Rollmann, E; Seidel, K; Sen, NE | 1 |
| Brandt, AU; Doss, S; Endres, M; Oberwahrenbrock, T; Paul, F; Rinnenthal, JL | 1 |
| Clark, HB; Demirgöz, D; Eberly, LE; Kittelson, E; Orr, HT; Öz, G; Rainwater, O | 1 |
| Adanyeguh, IM; Brice, A; Deelchand, DK; Durr, A; Eberly, LE; Emir, UE; Henry, PG; Jauffret, C; Mochel, F; Nguyen, TM; Öz, G; Rinaldi, D; Valabregue, R | 1 |
| Brandt, AU; Doss, S; Endres, M; Klockgether, T; Lux, S; Maul, S; Minnerop, M; Papazoglou, S; Paul, F; Rinnenthal, JL; Schmitz-Hübsch, T; Würfel, J | 1 |
| Bushara, KO; Clark, HB; Eberly, LE; Gomez, CM; Gross, MD; Hutter, D; Jiang, H; Oz, G; Tkác, I | 1 |
| Chen, HC; Lirng, JF; Soong, BW; Wang, PS; Wu, HM; Wu, YT | 1 |
| Belli, G; Cosottini, M; De Grandis, D; Della Nave, R; Filla, A; Foresti, S; Ginestroni, A; Guerrini, L; Lolli, F; Mascalchi, M; Piacentini, S; Plasmati, R; Salvi, F; Siciliano, G; Tessa, C | 1 |
| Färkkilä, M; Häkkinen, AM; Harno, H; Heikkinen, S; Kallela, M; Kaunisto, MA; Lundbom, N; Wessman, M | 1 |
| Ishikawa, K; Nakano, I; Nakao, K; Shimazaki, H; Takiyama, Y | 1 |
| Boesch, SM; Felber, S; Schocke, M; Seppi, K; Wenning, GK; Wolf, C | 1 |
| Borkert, J; Döhlinger, S; Hauser, TK; Luft, AR; Schulz, JB | 1 |
| Aichner, FT; Boesch, SM; Bürk, K; Felber, S; Fornai, F; Hollosi, P; Poewe, W; Schocke, M | 1 |
1 trial(s) available for n-acetylaspartic acid and Autosomal Dominant Cerebellar Ataxia, Type II
| Article | Year |
|---|---|
Differentiation of SCA2 from MSA-C using proton magnetic resonance spectroscopic imaging.
Topics: Adult; Age of Onset; Aged; Aspartic Acid; Cerebellum; Choline; Creatine; Diagnosis, Differential; Female; Humans; Image Processing, Computer-Assisted; Imaging, Three-Dimensional; Lactic Acid; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Middle Aged; Multiple System Atrophy; Reference Values; Severity of Illness Index; Spinocerebellar Ataxias; Time Factors | 2007 |
13 other study(ies) available for n-acetylaspartic acid and Autosomal Dominant Cerebellar Ataxia, Type II
| Article | Year |
|---|---|
Neurochemical abnormalities in premanifest and early spinocerebellar ataxias.
Topics: Activities of Daily Living; Adult; Aged; Aspartic Acid; Ataxins; Brain; Brain Diseases, Metabolic; Case-Control Studies; Cohort Studies; Cross-Sectional Studies; Disease Progression; Female; gamma-Aminobutyric Acid; Glutamic Acid; Humans; Inositol; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Middle Aged; Spinocerebellar Ataxias; Young Adult | 2018 |
Generation of an Atxn2-CAG100 knock-in mouse reveals N-acetylaspartate production deficit due to early Nat8l dysregulation.
Topics: Acetyltransferases; Animals; Aspartic Acid; Ataxin-2; Brain; Female; Gene Knock-In Techniques; Male; Mice; Mice, Transgenic; Spinocerebellar Ataxias; Trinucleotide Repeats | 2019 |
Metabolic evidence for cerebral neurodegeneration in spinocerebellar ataxia type 1.
Topics: Adult; Aged; Analysis of Variance; Aspartic Acid; Brain; Cerebral Cortex; Choline; Creatine; Female; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Nerve Degeneration; Nerve Fibers, Myelinated; Spinocerebellar Ataxias | 2014 |
Assessing recovery from neurodegeneration in spinocerebellar ataxia 1: Comparison of in vivo magnetic resonance spectroscopy with motor testing, gene expression and histology.
Topics: Animals; Area Under Curve; Aspartic Acid; Ataxin-1; Cerebellum; Doxycycline; Gene Expression; Humans; Inositol; Magnetic Resonance Spectroscopy; Male; Mice, Transgenic; Motor Activity; Polymerase Chain Reaction; Recovery of Function; ROC Curve; Rotarod Performance Test; Sensitivity and Specificity; Spinocerebellar Ataxias | 2015 |
In vivo neurometabolic profiling in patients with spinocerebellar ataxia types 1, 2, 3, and 7.
Topics: Adult; Aspartic Acid; Ataxins; Cohort Studies; Female; Glutamic Acid; Humans; Machado-Joseph Disease; Magnetic Resonance Spectroscopy; Male; Middle Aged; Principal Component Analysis; Protons; Spinocerebellar Ataxias; Statistics as Topic | 2015 |
Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency.
Topics: Adult; Aged; Aspartic Acid; Cerebellum; Cerebral Cortex; Creatine; Female; Glutamic Acid; Glutathione; Humans; Male; Middle Aged; Proton Magnetic Resonance Spectroscopy; Spinocerebellar Ataxias | 2015 |
Neurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status.
Topics: Analysis of Variance; Aspartic Acid; Brain Chemistry; Case-Control Studies; Female; Functional Laterality; Glial Fibrillary Acidic Protein; Humans; Inositol; Isoprostanes; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Middle Aged; Phosphocreatine; Protons; Severity of Illness Index; Spinocerebellar Ataxias; Statistics as Topic | 2010 |
Association between proton magnetic resonance spectroscopy measurements and CAG repeat number in patients with spinocerebellar ataxias 2, 3, or 6.
Topics: Adult; Age of Onset; Aged; Aspartic Acid; Case-Control Studies; Cerebellum; Creatine; Disease Progression; Female; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Nerve Tissue Proteins; Research Design; Retrospective Studies; Severity of Illness Index; Spinocerebellar Ataxias; Taiwan; Trinucleotide Repeats | 2012 |
Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study.
Topics: Adult; Aged; Aspartic Acid; Biomarkers; Brain Stem; Cerebellum; Creatine; Female; Humans; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Middle Aged; Pons; Severity of Illness Index; Spinocerebellar Ataxias | 2004 |
Decreased cerebellar total creatine in episodic ataxia type 2: a 1H MRS study.
Topics: Adolescent; Adult; Aspartic Acid; Calcium Channels; Cerebellum; Child; Choline; Creatine; Dysarthria; Female; Humans; Lactates; Magnetic Resonance Spectroscopy; Male; Nystagmus, Pathologic; RNA Splice Sites; Spinocerebellar Ataxias | 2005 |
[A case of spinocerebellar ataxia type 6 with its initial symptom of episodic ataxia-like phenotype].
Topics: Adult; Aspartic Acid; Brain Chemistry; Creatine; Female; Humans; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Spinocerebellar Ataxias | 2006 |
Magnetic resonance imaging in spinocerebellar ataxias.
Topics: Aspartic Acid; Ataxin-1; Ataxin-3; Ataxins; Atrophy; Brain; Cerebellum; Humans; Magnetic Resonance Imaging; Nerve Tissue Proteins; Nuclear Proteins; Repressor Proteins; Sensitivity and Specificity; Spinocerebellar Ataxias | 2008 |
Proton magnetic resonance spectroscopic imaging reveals differences in spinocerebellar ataxia types 2 and 6.
Topics: Adult; Aspartic Acid; Choline; Creatine; Female; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Mutation; Protons; Spinocerebellar Ataxias; Statistics, Nonparametric | 2001 |