Page last updated: 2024-08-17

aspartic acid and Autosomal Dominant Cerebellar Ataxia, Type II

aspartic acid has been researched along with Autosomal Dominant Cerebellar Ataxia, Type II in 16 studies

Research

Studies (16)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	7 (43.75)	29.6817
2010's	9 (56.25)	24.3611
2020's	0 (0.00)	2.80

Authors

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
Agrawal, S; Andresen, M; Barnes, J; Duvick, L; Ebner, B; Giesler, GJ; Lim, J; Orr, HT; Zoghbi, HY	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
Ikeda, SI; Morita, H; Suzuki, K; Yoshida, K	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

Trials

1 trial(s) available for aspartic acid and Autosomal Dominant Cerebellar Ataxia, Type II

Article	Year
Differentiation of SCA2 from MSA-C using proton magnetic resonance spectroscopic imaging. Journal of magnetic resonance imaging : JMRI, 2007, Volume: 25, Issue:3 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

Article

Year

Differentiation of SCA2 from MSA-C using proton magnetic resonance spectroscopic imaging.

Journal of magnetic resonance imaging : JMRI, 2007, Volume: 25, Issue:3

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

Other Studies

15 other study(ies) available for aspartic acid and Autosomal Dominant Cerebellar Ataxia, Type II

Article	Year
Neurochemical abnormalities in premanifest and early spinocerebellar ataxias. Annals of neurology, 2018, Volume: 83, Issue:4 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. Neurobiology of disease, 2019, Volume: 132 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. Cerebellum (London, England), 2014, Volume: 13, Issue:2 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. Neurobiology of disease, 2015, Volume: 74 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. Movement disorders : official journal of the Movement Disorder Society, 2015, Apr-15, Volume: 30, Issue:5 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. Journal of neurology, 2015, Volume: 262, Issue:8 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. Movement disorders : official journal of the Movement Disorder Society, 2010, Jul-15, Volume: 25, Issue:9 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
SCA1-like disease in mice expressing wild-type ataxin-1 with a serine to aspartic acid replacement at residue 776. Neuron, 2010, Sep-23, Volume: 67, Issue:6 Topics: Animals; Aspartic Acid; Ataxin-1; Ataxins; Calbindins; Cerebellum; Dendrites; Disease Models, Animal; Gene Expression Regulation; Mice; Mice, Transgenic; Motor Activity; Mutation; Nerve Tissue Proteins; Neural Pathways; Nuclear Proteins; Purkinje Cells; Rotarod Performance Test; S100 Calcium Binding Protein G; Serine; Spinocerebellar Ataxias; Vesicular Glutamate Transport Protein 2	2010
Association between proton magnetic resonance spectroscopy measurements and CAG repeat number in patients with spinocerebellar ataxias 2, 3, or 6. PloS one, 2012, Volume: 7, Issue:10 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. Brain : a journal of neurology, 2004, Volume: 127, Issue:Pt 8 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. Neurology, 2005, Feb-08, Volume: 64, Issue:3 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]. No to shinkei = Brain and nerve, 2006, Volume: 58, Issue:1 Topics: Adult; Aspartic Acid; Brain Chemistry; Creatine; Female; Humans; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Spinocerebellar Ataxias	2006
A Japanese case of SCA14 with the Gly128Asp mutation. Journal of human genetics, 2006, Volume: 51, Issue:12 Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Aspartic Acid; Base Sequence; Cerebellum; Female; Glycine; Humans; Japan; Middle Aged; Molecular Sequence Data; Point Mutation; Protein Kinase C; Radiography; Spinocerebellar Ataxias	2006
Magnetic resonance imaging in spinocerebellar ataxias. Cerebellum (London, England), 2008, Volume: 7, Issue:2 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. Journal of magnetic resonance imaging : JMRI, 2001, Volume: 13, Issue:4 Topics: Adult; Aspartic Acid; Choline; Creatine; Female; Humans; Magnetic Resonance Spectroscopy; Male; Middle Aged; Mutation; Protons; Spinocerebellar Ataxias; Statistics, Nonparametric	2001