threonine has been researched along with Aura in 10 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (20.00) | 18.7374 |
1990's | 1 (10.00) | 18.2507 |
2000's | 3 (30.00) | 29.6817 |
2010's | 4 (40.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Donovan, MJ; Gietzen, DW; Lindström, SH; Sharp, JW; Teh, PS | 1 |
Kumar, P; Rai, V | 1 |
Bao, X; Downs, J; Leonard, H; Williams, S; Wong, K | 1 |
Baulac, S; Ishida, S; Kaneko, S; Kuwamura, M; Mashimo, T; Nishio, T; Ohno, Y; Sakamoto, Y; Serikawa, T; Takizawa, A | 1 |
Imoto, K; Obata, K; Yamagata, Y | 1 |
Janjua, NA; MacGibbon, B; Metrakos, JD; Metrakos, K; van Gelder, NM | 1 |
Kitoh, J; Kuroda, T; Masuda, K; Mizobuchi, M; Nakano, K; Takahashi, S | 1 |
Hadama, A; Hayashibara, M; Higuchi, S; Ieiri, I; Kitada, M; Mamiya, K; Morita, T; Ninomiya, H; Ohmori, S; Otsubo, K; Tainaka, H; Tashiro, N | 1 |
Apeland, T; Mansoor, MA; Strandjord, RE | 1 |
Iivanainen, M; Palo, J; Savolainen, H | 1 |
1 review(s) available for threonine and Aura
Article | Year |
---|---|
Methylenetetrahydrofolate reductase C677T polymorphism and susceptibility to epilepsy.
Topics: Cysteine; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Male; Methylenetetrahydrofolate Reductase (NADPH2); Odds Ratio; Polymorphism, Single Nucleotide; Risk Factors; Threonine | 2018 |
9 other study(ies) available for threonine and Aura
Article | Year |
---|---|
Indispensable Amino Acid-Deficient Diets Induce Seizures in Ketogenic Diet-Fed Rodents, Demonstrating a Role for Amino Acid Balance in Dietary Treatments for Epilepsy.
Topics: Amino Acids, Essential; Animals; Brain; Deficiency Diseases; Diet, Ketogenic; Dietary Proteins; Epilepsy; Feeding Behavior; Female; Gerbillinae; Glutamic Acid; Male; Nutritional Requirements; Rats, Sprague-Dawley; Seizures; Threonine | 2018 |
Using a large international sample to investigate epilepsy in Rett syndrome.
Topics: Adolescent; Adult; Age Factors; Age of Onset; Anticonvulsants; Arginine; Child; Child, Preschool; Cysteine; Epilepsy; Female; Gene Deletion; Genotype; Humans; Infant; Internationality; Methionine; Methyl-CpG-Binding Protein 2; Middle Aged; Mutation; Odds Ratio; Phenotype; Polymorphism, Single Nucleotide; Rett Syndrome; Sampling Studies; Severity of Illness Index; Threonine | 2013 |
Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures.
Topics: Animals; Antiemetics; Biophysical Phenomena; Biotinylation; Body Weight; Carbamazepine; Cells, Cultured; Chromosome Mapping; Disease Models, Animal; DNA Mutational Analysis; Electric Stimulation; Electroencephalography; Electromyography; Epilepsy; Ethylnitrosourea; Gene Transfer Techniques; Humans; Isaacs Syndrome; Kv1.1 Potassium Channel; Male; Membrane Potentials; Mice; Models, Molecular; Mutagenesis; Mutagens; Mutation, Missense; Myokymia; Oocytes; Patch-Clamp Techniques; Protein Transport; Psychomotor Performance; Rats; Rats, Inbred F344; Rats, Mutant Strains; Sequence Analysis; Serine; Survival Analysis; Swimming; Threonine; Time Factors; Xenopus | 2012 |
A mechanism for the inactivation of Ca2+/calmodulin-dependent protein kinase II during prolonged seizure activity and its consequence after the recovery from seizure activity in rats in vivo.
Topics: Animals; Brain; Calcium; Calcium Signaling; Calcium-Calmodulin-Dependent Protein Kinase Type 2; Calcium-Calmodulin-Dependent Protein Kinases; Cell Membrane; Convulsants; Disease Models, Animal; Enzyme Activation; Epilepsy; Kainic Acid; Male; Membrane Potentials; Neurons; Phosphorylation; Rats; Rats, Wistar; Recovery of Function; Solubility; Status Epilepticus; Threonine | 2006 |
Plasma amino acids in 3/sec spike-wave epilepsy.
Topics: Adolescent; Adult; Alanine; Amino Acids; Aspartic Acid; Child; Child, Preschool; Epilepsy; Female; Glutamates; Glutamine; Glycine; Humans; Isoleucine; Leucine; Male; Methionine; Middle Aged; Phenylalanine; Serine; Taurine; Threonine; Tyrosine; Valine | 1980 |
High levels of quinolinic acid in brain of epilepsy-prone E1 mice.
Topics: Aging; Amino Acids; Animals; Cerebral Cortex; Epilepsy; Escherichia coli; Lipopolysaccharides; Methionine; Mice; Mice, Inbred Strains; Mice, Neurologic Mutants; Quinolinic Acid; Species Specificity; Threonine; Tryptophan | 1993 |
Catalytic activity of three variants (Ile, Leu, and Thr) at amino acid residue 359 in human CYP2C9 gene and simultaneous detection using single-strand conformation polymorphism analysis.
Topics: Adult; Alleles; Amino Acid Substitution; Anti-Inflammatory Agents, Non-Steroidal; Aryl Hydrocarbon Hydroxylases; Blotting, Western; Catalysis; Cytochrome P-450 CYP2C9; Cytochrome P-450 Enzyme System; Diclofenac; Epilepsy; Genetic Variation; Humans; Isoenzymes; Isoleucine; Kinetics; Leucine; Male; Middle Aged; Mutagenesis, Site-Directed; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Recombinant Proteins; Steroid 16-alpha-Hydroxylase; Steroid Hydroxylases; Threonine | 2000 |
Antiepileptic drugs as independent predictors of plasma total homocysteine levels.
Topics: Adult; Amino Acid Substitution; Anticonvulsants; Cholesterol; Cholesterol, HDL; Confidence Intervals; Cysteine; Epilepsy; Fasting; Female; Folic Acid; Homocysteine; Humans; Hyperhomocysteinemia; Male; Middle Aged; Mutation; Predictive Value of Tests; Prevalence; Statistics, Nonparametric; Threonine; Triglycerides; Vitamin B 12 | 2001 |
Free amino acids and carbohydrates in the cerebrospinal fluid of 305 mentally retarded patients: a screening study.
Topics: Adolescent; Adult; Alanine; Amino Acids; Arginine; Carbohydrates; Child; Child, Preschool; Chromatography, Thin Layer; Cystine; Epilepsy; Female; Glutamates; Glutamine; Humans; Intellectual Disability; Intelligence Tests; Isoleucine; Leucine; Lysine; Male; Metabolism, Inborn Errors; Methionine; Middle Aged; Ornithine; Phenylalanine; Pneumoencephalography; Threonine; Valine | 1973 |