arginine has been researched along with Ataxia in 17 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (41.18) | 18.7374 |
| 1990's | 1 (5.88) | 18.2507 |
| 2000's | 4 (23.53) | 29.6817 |
| 2010's | 3 (17.65) | 24.3611 |
| 2020's | 2 (11.76) | 2.80 |
| Authors | Studies |
|---|---|
| Barmada, SJ; Barsur, V; Flores, BN; Ivanova, MI; Koutmou, KS; Krans, A; Monroe, J; Rodriguez, CM; Todd, PK; Wright, SE; Xing, J | 1 |
| Anshari, ZR; Colucci, E; Guskov, A; Nemchinova, M; Patiño-Ruiz, MF; Slotboom, DJ; Whittaker, J | 1 |
| Attri, S; Saini, AG; Sankhyan, N; Singhi, P | 1 |
| Dupré, N; Lu, JP; Rouleau, GA; Sliter, DA; Wojcikiewicz, RJ; Wright, FA | 1 |
| Bersano, A; Di Cristofori, A; Fusi, L; Gomitoni, A; Grampa, G | 1 |
| Ceuterick, C; De Jonghe, P; Dehaene, I; Dermaut, B; Löfgren, A; Martin, JJ; Moonen, M; Tack, P; Van Broeckhoven, C; Van Goethem, G; Van Zandijcke, M; Ververken, D; Wibail, A | 1 |
| DEHEVESY, G; HAMBRAEUS, L | 1 |
| Bouchard, JP; Brais, B; Dicaire, MJ; Duquette, A; Gosselin, I; Labuda, D; Loisel, L; Marchand, L; Mathieu, J; McNabb-Baltar, J; Roddier, K; St-Denis, A | 1 |
| Appleton, D; Coman, D; Jaeken, J; Klingberg, S; MacDonald, R; McGill, J; Morris, D | 1 |
| Furukawa, H; Nabeshima, T; Noda, Y; Yamada, K | 1 |
| Morato, GS; Wazlawik, E | 1 |
| Potter, JL; Silvidi, AA; Timmons, GD; West, R | 1 |
| Brenton, DP; Cusworth, DC; Hartley, S; Kuzemko, JA; Lumley, S | 1 |
| Breglia, RJ; Jarowski, CI; Ward, CO | 1 |
| Lewis, PD; Miller, AL | 1 |
| O'Dell, BL; Savage, JE; Stutz, MW | 1 |
| Greer, M; Sprinkle, T; Williams, CM | 1 |
1 review(s) available for arginine and Ataxia
| Article | Year |
|---|---|
R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update.
Topics: Arginine; Ataxia; Calcium Channels; Cerebellum; DNA Mutational Analysis; Female; Glutamine; Humans; Middle Aged; Migraine with Aura; Radiography; Tomography Scanners, X-Ray Computed | 2012 |
16 other study(ies) available for arginine and Ataxia
| Article | Year |
|---|---|
CGG repeats trigger translational frameshifts that generate aggregation-prone chimeric proteins.
Topics: Arginine; Ataxia; Fragile X Mental Retardation Protein; Fragile X Syndrome; Glycine; Humans; Neurodegenerative Diseases; Peptides; Protein Aggregation, Pathological; Recombinant Fusion Proteins; Trinucleotide Repeats | 2022 |
Mutation in glutamate transporter homologue GltTk provides insights into pathologic mechanism of episodic ataxia 6.
Topics: Amino Acid Transport System X-AG; Archaea; Archaeal Proteins; Arginine; Ataxia; Excitatory Amino Acid Transporter 1; Humans; Mutation | 2023 |
Hypomorphic citrullinaemia due to mutated
Topics: Administration, Oral; Arginine; Ataxia; Child; Citrullinemia; Diet, Protein-Restricted; Genetic Testing; High-Throughput Nucleotide Sequencing; Humans; Male; Mutation, Missense; Sodium Benzoate | 2018 |
A Point Mutation in the Ubiquitin Ligase RNF170 That Causes Autosomal Dominant Sensory Ataxia Destabilizes the Protein and Impairs Inositol 1,4,5-Trisphosphate Receptor-mediated Ca2+ Signaling.
Topics: Animals; Arginine; Ataxia; Calcium; Calcium Signaling; Cell Line; Cell Membrane; Endoplasmic Reticulum; Exons; HeLa Cells; Humans; Inositol 1,4,5-Trisphosphate Receptors; Lysine; Mice; Mutation; Neurodegenerative Diseases; Point Mutation; Proteasome Endopeptidase Complex; Signal Transduction; Ubiquitin; Ubiquitin-Protein Ligases | 2015 |
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia.
Topics: Adolescent; Adult; Aged; Arginine; Ataxia; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Electron Transport Complex IV; Female; Genes, Recessive; Heterozygote; Humans; Magnetic Resonance Imaging; Male; Microscopy, Electron; Middle Aged; Molecular Sequence Data; Muscle, Skeletal; Mutation, Missense; Ophthalmoplegia, Chronic Progressive External; Pedigree; Succinate Dehydrogenase; Tryptophan | 2003 |
CYSTINURIA IN SWEDEN. VIII. A CASE OF COELIAC DISEASE ASSOCIATED WITH CYSTINE-LYSINURIA.
Topics: Amino Acid Metabolism, Inborn Errors; Arginine; Ataxia; Celiac Disease; Chromatography; Creatine; Creatinine; Cystinuria; Electrophoresis; Glucose Tolerance Test; Humans; Infant; Intestine, Small; Intestines; Lysine; Muscle Spasticity; Ornithine; Proteins; Psychomotor Disorders; Renal Aminoacidurias; Sweden; Urine; Vitamin A; Xylose | 1964 |
Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy.
Topics: Adult; Aged; alpha-Fetoproteins; Apraxias; Arginine; Ataxia; Chromosomes, Human, Pair 9; Cluster Analysis; DNA Helicases; DNA Mutational Analysis; Family Health; Female; Glutamic Acid; Humans; Leucine; Linkage Disequilibrium; Lysine; Male; Middle Aged; Multifunctional Enzymes; Mutation; Oculomotor Nerve Diseases; Quebec; RNA Helicases | 2005 |
Congenital disorder of glycosylation type 1a: three siblings with a mild neurological phenotype.
Topics: Adult; Arginine; Ataxia; Cerebellar Diseases; Congenital Disorders of Glycosylation; Female; Histidine; Humans; Intellectual Disability; Lysine; Magnetic Resonance Imaging; Male; Mutation; Osteoporosis; Phenotype; Phosphotransferases (Phosphomutases); Siblings | 2007 |
Involvement of nitric oxide in phencyclidine-induced hyperlocomotion in mice.
Topics: Animals; Arginine; Ataxia; Lysine; Male; Mice; Motor Activity; NG-Nitroarginine Methyl Ester; Nitric Oxide; Phencyclidine | 1995 |
Effects of intracerebroventricular administration of 7-nitroindazole on tolerance to ethanol.
Topics: Animals; Arginine; Ataxia; Drug Tolerance; Enzyme Inhibitors; Ethanol; Hypothermia; Indazoles; Injections, Intraventricular; Male; Nerve Tissue Proteins; Neuroprotective Agents; Nitric Oxide; Nitric Oxide Synthase; Nitric Oxide Synthase Type II; Rats; Rats, Wistar; Stereoisomerism | 2002 |
Arginosuccinicaciduria. The hair abnormality.
Topics: Amino Acids; Ammonia; Arginine; Ataxia; Blood Urea Nitrogen; Child, Preschool; Chromatography, Paper; Cystine; Electroencephalography; Epilepsy, Tonic-Clonic; Female; Hair; Humans; Intellectual Disability; Metabolism, Inborn Errors; Stress, Mechanical; Succinates; Syndrome | 1974 |
Argininosuccinicaciduria: clinical, metabolic and dietary study.
Topics: Affective Symptoms; Amino Acid Metabolism, Inborn Errors; Ammonia; Arginase; Arginine; Ataxia; Child; Citrulline; Dietary Proteins; Electroencephalography; Epilepsy; Female; Humans; Intellectual Disability; Intelligence Tests; Male; Ornithine; Phenobarbital; Seizures; Succinates; Tremor | 1974 |
Effect of selected amino acids on ethanol toxicity in rats.
Topics: Administration, Oral; Alcoholic Intoxication; Amino Acids; Animals; Arginine; Ataxia; Central Nervous System; Drug Interactions; Ethanol; Female; Glycine; Humans; Hydrogen-Ion Concentration; Lethal Dose 50; Lysine; Male; Ornithine; Rats; Sleep; Time Factors | 1973 |
Argininosuccinic aciduria. Case report with neuropathological findings.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Arginine; Ataxia; Autopsy; Brain; Cerebral Cortex; Epilepsy; Humans; Intellectual Disability; Liver; Lyases; Male; Pedigree; Sleep Wake Disorders; Succinates; Thalamus | 1970 |
Relation of dietary cations to arginine-lysine antagonism and free amino acid patterns in chicks.
Topics: Amino Acids; Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Arginine; Ataxia; Caseins; Chickens; Chlorides; Dietary Proteins | 1971 |
Detection of argininosuccinic aciduria by gas chromatography.
Topics: Arginine; Aspartic Acid; Ataxia; Chemical Precipitation; Chromatography, Gas; Epilepsy; Esters; Humans; Hydrogen-Ion Concentration; Intellectual Disability; Liver Diseases; Metabolism, Inborn Errors; Methods; Ornithine; Spectrum Analysis; Succinates | 1969 |