lysine and Ataxia
lysine has been researched along with Ataxia in 10 studies
Research
Studies (10)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (40.00) | 18.7374 |
| 1990's | 1 (10.00) | 18.2507 |
| 2000's | 3 (30.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| Dupré, N; Lu, JP; Rouleau, GA; Sliter, DA; Wojcikiewicz, RJ; Wright, FA | 1 |
| Hennessy, M; Mayne, PD; McCarthy, P; Murphy, S; Saidha, S | 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 |
| Bieganowski, P; Brenner, C; Seidle, HF | 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 |
| Frey, HJ; Frey, ML; Riekkinen, PJ; Tuomola, HO | 1 |
| Breglia, RJ; Jarowski, CI; Ward, CO | 1 |
| Efron, ML; Moser, HW; Shih, VE | 1 |
Other Studies
10 other study(ies) available for lysine and Ataxia
| Article | Year |
|---|---|
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 |
L-2-hydroxyglutaric aciduria diagnosed in an adult presenting with acute deterioration.
Topics: Adult; Ataxia; Brain; Disease Progression; Epilepsy; Glutarates; Humans; Lysine; Male; Metabolism, Inborn Errors; Rare Diseases; Seizures | 2010 |
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 |
Disease-associated mutations inactivate AMP-lysine hydrolase activity of Aprataxin.
Topics: Adenosine Monophosphate; Alleles; Apraxias; Ataxia; Binding Sites; Blotting, Western; Cations; DNA Damage; DNA-Binding Proteins; Electrophoresis, Polyacrylamide Gel; Escherichia coli; Eye Diseases; Humans; Hydrogen-Ion Concentration; Hydrolases; Kinetics; Lysine; Metals; Motor Neuron Disease; Mutagenesis, Site-Directed; Mutation; Nuclear Proteins; Phenotype; Plasmids; Protein Binding; Protein Structure, Tertiary; RNA, Messenger; Substrate Specificity; Syndrome; Temperature; Zinc Fingers | 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 |
A family with autosomal dominant spinocerebellar ataxia, with electrophysiological findings.
Topics: Action Potentials; Adult; Aged; Ataxia; Beta-Globulins; Cerebellar Ataxia; Electromyography; Female; Foot Deformities, Congenital; Histidine; Humans; Lysine; Male; Methods; Middle Aged; Neural Conduction; Nystagmus, Pathologic; Optic Atrophy; Pedigree | 1973 |
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 |
Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Ataxia; Child, Preschool; Citrulline; Diet Therapy; Humans; Intellectual Disability; Lysine; Male; Myoclonus; Ornithine; Ornithine Carbamoyltransferase; Seizures | 1969 |