isoleucine has been researched along with Epilepsy in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (20.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cheng, P; Jia, P; Liao, S; Meng, K; Xiao, C; Xu, R; Zhao, X; Zheng, X | 1 |
| Feng, Z; Li, X; Lin, R; Liu, L; Sheng, H; Su, L | 1 |
| Chen, P; Lu, A; Xu, H; Yan, Q; Zhao, P | 1 |
| Fujiwara, T; Iai, M; Inoue, Y; Iwamoto, H; Kaneko, S; Kurosawa, K; Mazaki, E; Ogiwara, I; Okamura, N; Osaka, H; Yamada, M; Yamakawa, K; Yamashita, S; Yasui-Furukori, N | 1 |
| Martin, JK; Norman, RM | 1 |
| Janjua, NA; MacGibbon, B; Metrakos, JD; Metrakos, K; van Gelder, NM | 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 |
| Brown, GK; Danks, DM; Hunt, SM; Mitchell, DK | 1 |
| Ionasescu, V; Mueller, S; Stegink, L; Weinstein, M | 1 |
| Iivanainen, M; Palo, J; Savolainen, H | 1 |
1 review(s) available for isoleucine and Epilepsy
| Article | Year |
|---|---|
The effects of ABCC2 G1249A polymorphism on the risk of resistance to antiepileptic drugs: a meta-analysis of the literature.
Topics: Amino Acid Substitution; Anticonvulsants; Drug Resistance; Epilepsy; Humans; Isoleucine; Multidrug Resistance-Associated Protein 2; Multidrug Resistance-Associated Proteins; Polymorphism, Single Nucleotide; Risk Factors; Valine | 2014 |
9 other study(ies) available for isoleucine and Epilepsy
| Article | Year |
|---|---|
Insights into the development of pentylenetetrazole-induced epileptic seizures from dynamic metabolomic changes.
Topics: Alanine; Animals; Anticonvulsants; Asparagine; Citrates; Creatine; Creatinine; Disease Models, Animal; Epilepsy; Glucose; Glutamates; Isoleucine; Ketone Bodies; Lactates; Leucine; Pentylenetetrazole; Pyruvates; Rats; Seizures; Succinates; Valine | 2022 |
Clinical and molecular analysis of 6 Chinese patients with isoleucine metabolism defects: identification of 3 novel mutations in the HSD17B10 and ACAT1 gene.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acetyl-CoA C-Acetyltransferase; Acetyl-CoA C-Acyltransferase; Amino Acid Metabolism, Inborn Errors; Brain; Child, Preschool; China; Diagnosis, Differential; Dyskinesias; Epilepsy; Female; Humans; Infant; Isoleucine; Male; Mental Retardation, X-Linked; Models, Molecular; Mutation; Retrospective Studies | 2017 |
Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation.
Topics: Adult; Child; DNA Mutational Analysis; Epilepsy; Female; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Mutation; NAV1.1 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Pedigree; Phenotype; Sodium Channels; Valine | 2007 |
Maple syrup urine disease in an infant with microgyria.
Topics: Brain; Cerebral Cortex; Chromatography, Paper; Epilepsy; Female; Humans; Infant; Infant, Newborn; Isoleucine; Leucine; Maple Syrup Urine Disease; Pons; Spasm; Thalamus; Valine | 1967 |
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 |
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 |
Profound neurological illness, relieved by protein restriction, in a baby with a transient disturbance in the metabolism of ingested isoleucine.
Topics: Amino Acid Metabolism, Inborn Errors; Developmental Disabilities; Dietary Proteins; Epilepsy; Female; Humans; Infant; Isoleucine; Muscle Hypotonia; Nervous System Diseases | 1987 |
Amino acid abnormality in Sjögren-Larsson syndrome.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Dental Enamel Hypoplasia; Epilepsy; Ethylamines; Glutamine; Glycine; Histidine; Humans; Ichthyosis; Intellectual Disability; Isoleucine; Leucine; Lysine; Male; Muscle Spasticity; Retinal Degeneration; Serine; Syndrome; Valine | 1973 |
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 |