glutamic acid has been researched along with Adiadochokinesis in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (33.33) | 18.7374 |
| 1990's | 1 (8.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 6 (50.00) | 24.3611 |
| 2020's | 1 (8.33) | 2.80 |
| Authors | Studies |
|---|---|
| Boiko, N; Harbidge, DG; Kreko-Pierce, T; Marcus, DC; Pugh, JR; Stockand, JD | 1 |
| Klopstock, T; Rudolph, G; Stendel, C; Wagner, M | 1 |
| Bazán, E; Calatrava-Ferreras, L; Casarejos, MJ; Díaz-Gil, JJ; Gonzalo-Gobernado, R; Herranz, AS; Jiménez-Escrig, A; Montero-Vega, MT; Reimers, D | 1 |
| Hardy, J; Houlden, H; Schorge, S; Singleton, A; van de Leemput, J | 1 |
| Di Guilmi, MN; Ferrari, MD; Forsythe, ID; Inchauspe, CG; Uchitel, OD; Urbano, FJ; van den Maagdenberg, AM | 1 |
| Fahlke, C; Kovermann, P; Winter, N | 1 |
| Barcs, G; Finta, L; Holló, A; Kamondi, A; Osztie, E; Papp, E; Sólyom, A; Szucs, A; Várallyay, P; Varga, D | 1 |
| Mizuno, Y; Tanaka, Y | 1 |
| Perry, TL | 1 |
| Plaitakis, A | 1 |
| Nicklas, WJ | 1 |
| Itoyama, Y; Mochizuki, H; Takeda, A; Tanji, H; Tateyama, M | 1 |
2 review(s) available for glutamic acid and Adiadochokinesis
| Article | Year |
|---|---|
Abnormal metabolism of neuroexcitatory amino acids in olivopontocerebellar atrophy.
Topics: Amino Acids; Animals; Aspartic Acid; Cells, Cultured; Cerebellar Ataxia; Fibroblasts; Glutamate Dehydrogenase; Glutamates; Glutamic Acid; Humans; Malates; Olivary Nucleus; Phenotype; Pons; Rats; Skin; Syndrome | 1984 |
Amino acid metabolism in the central nervous system: role of glutamate dehydrogenase.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Central Nervous System; Cerebellar Ataxia; Enzyme Activation; gamma-Aminobutyric Acid; Glutamate Dehydrogenase; Glutamate Synthase; Glutamates; Glutamic Acid; Glutamine; Humans; Leucine; Mitochondria; NADP; Nerve Endings; Neuroglia; Rats; Syndrome | 1984 |
10 other study(ies) available for glutamic acid and Adiadochokinesis
| Article | Year |
|---|---|
Cerebellar Ataxia Caused by Type II Unipolar Brush Cell Dysfunction in the Asic5 Knockout Mouse.
Topics: Acid Sensing Ion Channels; Action Potentials; Animals; Cerebellar Ataxia; Glutamic Acid; Male; Mice; Neurons; Potassium | 2020 |
Gillespie's Syndrome with Minor Cerebellar Involvement and No Intellectual Disability Associated with a Novel ITPR1 Mutation: Report of a Case and Literature Review.
Topics: Aniridia; Atrophy; Cerebellar Ataxia; Cerebellum; Gait Disorders, Neurologic; Glutamic Acid; Humans; Infant; Inositol 1,4,5-Trisphosphate Receptors; Intellectual Disability; Male; Mutation; Mutation, Missense; Pedigree | 2019 |
Neuroprotective role of liver growth factor "LGF" in an experimental model of cerebellar ataxia.
Topics: Animals; Antigens, Nuclear; Bilirubin; Calbindins; Cell Differentiation; Cerebellar Ataxia; Cerebellum; Disease Models, Animal; Female; gamma-Aminobutyric Acid; Glutamic Acid; Microglia; Nerve Tissue Proteins; Neurons; Neuroprotective Agents; Proto-Oncogene Proteins c-bcl-2; Pyridines; Rats; Rats, Sprague-Dawley; Serum Albumin; Serum Albumin, Human | 2014 |
Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling.
Topics: Animals; Calcium; Calcium Channels, N-Type; Cerebellar Ataxia; Glutamic Acid; Humans; Inositol 1,4,5-Trisphosphate Receptors; Models, Biological; Mutation; Peptides; Potassium Channels; Purkinje Cells; Signal Transduction | 2010 |
Presynaptic CaV2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held.
Topics: Action Potentials; Animals; Auditory Pathways; Calcium; Calcium Channels, N-Type; Calcium Channels, P-Type; Calcium Channels, Q-Type; Cerebellar Ataxia; Chelating Agents; Excitatory Postsynaptic Potentials; Exocytosis; Glutamic Acid; Mice; Mice, Transgenic; Migraine Disorders; Mutation, Missense; Neuronal Plasticity; Neurons, Afferent; Pons; Potassium Channel Blockers; Presynaptic Terminals | 2012 |
A point mutation associated with episodic ataxia 6 increases glutamate transporter anion currents.
Topics: Cell Line; Cell Membrane; Cerebellar Ataxia; Excitatory Amino Acid Transporter 1; Glutamic Acid; Humans; Membrane Potentials; Point Mutation; Voltage-Dependent Anion Channels | 2012 |
Clinical experiences with Creutzfeldt-Jakob disease: three case studies.
Topics: Aged; Autopsy; Brain; Cerebellar Ataxia; Creutzfeldt-Jakob Syndrome; Diagnosis, Differential; Electroencephalography; Fatal Outcome; Female; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Prion Proteins; Prions; Seizures; Speech Disorders | 2012 |
[GABA, glutamate, aspartate, glycine, and taurine contents in spinocerebellar degeneration and parkinsonism].
Topics: Adult; Aged; Amino Acids; Aspartic Acid; Brain Chemistry; Cerebellar Ataxia; Chromatography, High Pressure Liquid; Female; gamma-Aminobutyric Acid; Glutamates; Glutamic Acid; Humans; Male; Middle Aged; Neurotransmitter Agents; Parkinson Disease; Taurine | 1984 |
Four biochemically different types of dominantly inherited olivopontocerebellar atrophy.
Topics: Adult; Aged; Amino Acids; Aspartic Acid; Brain Chemistry; Cerebellar Ataxia; gamma-Aminobutyric Acid; Genes, Dominant; Glutamates; Glutamic Acid; Humans; Middle Aged; Neurotransmitter Agents; Olivary Nucleus; Pons; Syndrome; Taurine | 1984 |
[Progressive cerebellar ataxia and distal amyotrophy of Charcot-Marie-Tooth type with hyperglutamataemia:two sibling cases].
Topics: Adult; Cerebellar Ataxia; Charcot-Marie-Tooth Disease; Female; Glutamic Acid; Humans; Male | 1995 |