arginine has been researched along with Adiadochokinesis in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Auta, J; Davis, JM; Gatta, E; Guidotti, A; Pandey, SC; Zhang, H | 1 |
| Gardner, RC; Schmahmann, JD | 1 |
| Ito, D; Kitamoto, T; Nishimoto, Y; Shimizu, T; Suzuki, N; Suzuki, S | 1 |
| Alonso, I; Barros, J; Coutinho, P; Seixas, A; Sequeiros, J; Silveira, I; Tuna, A | 1 |
| Hambraeus, L; Hardell, LI; Hjorth, G; Lorentsson, R; Westphal, O | 1 |
5 other study(ies) available for arginine and Adiadochokinesis
| Article | Year |
|---|---|
Essential role for neuronal nitric oxide synthase in acute ethanol-induced motor impairment.
Topics: Alcohol-Induced Disorders, Nervous System; Animals; Arginine; Cerebellar Ataxia; Cerebellum; Enzyme Inhibitors; Ethanol; Frontal Lobe; Indazoles; Male; Nitric Oxide Synthase Type I; Psychomotor Disorders; Rats, Sprague-Dawley | 2020 |
Arginine test is not reliable for diagnosing cerebellar multiple system atrophy.
Topics: Adult; Arginine; Biomarkers; Blood Chemical Analysis; Cerebellar Ataxia; Diagnosis, Differential; Female; Growth Hormone; Humans; Male; Middle Aged; Multiple System Atrophy; Predictive Value of Tests; Reproducibility of Results; Sensitivity and Specificity | 2010 |
Slow-progressive ataxia with a methionine-to-arginine point mutation in codon 232 in the prion protein gene (PRNP).
Topics: Arginine; Cerebellar Ataxia; Cerebral Angiography; Creutzfeldt-Jakob Syndrome; Electroencephalography; Female; Humans; Magnetic Resonance Angiography; Magnetic Resonance Imaging; Methionine; Middle Aged; Point Mutation; Prion Proteins; Prions; Tomography, Emission-Computed, Single-Photon; Vision Disorders | 2011 |
A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel alpha-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine.
Topics: Adolescent; Adult; Arginine; Calcium Channels; Cerebellar Ataxia; Child; DNA Mutational Analysis; Exons; Female; Hemiplegia; Humans; Male; Migraine Disorders; Pedigree; Point Mutation | 2004 |
Argininosuccinic aciduria. Report of three cases and the effect of high and reduced protein intake on the clinical state.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Arginine; Blood Urea Nitrogen; Cerebellar Ataxia; Child; Developmental Disabilities; Diet Therapy; Dietary Proteins; Electroencephalography; Female; Hair; Humans; Intellectual Disability; Succinates | 1974 |