isoleucine and Epilepsy

isoleucine has been researched along with Epilepsy in 10 studies

Research

Studies (10)

TimeframeStudies, this research(%)All Research%
pre-19905 (50.00)18.7374
1990's0 (0.00)18.2507
2000's2 (20.00)29.6817
2010's2 (20.00)24.3611
2020's1 (10.00)2.80

Authors

AuthorsStudies
Cheng, P; Jia, P; Liao, S; Meng, K; Xiao, C; Xu, R; Zhao, X; Zheng, X1
Feng, Z; Li, X; Lin, R; Liu, L; Sheng, H; Su, L1
Chen, P; Lu, A; Xu, H; Yan, Q; Zhao, P1
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, N1
Martin, JK; Norman, RM1
Janjua, NA; MacGibbon, B; Metrakos, JD; Metrakos, K; van Gelder, NM1
Hadama, A; Hayashibara, M; Higuchi, S; Ieiri, I; Kitada, M; Mamiya, K; Morita, T; Ninomiya, H; Ohmori, S; Otsubo, K; Tainaka, H; Tashiro, N1
Brown, GK; Danks, DM; Hunt, SM; Mitchell, DK1
Ionasescu, V; Mueller, S; Stegink, L; Weinstein, M1
Iivanainen, M; Palo, J; Savolainen, H1

Reviews

1 review(s) available for isoleucine and Epilepsy

ArticleYear
The effects of ABCC2 G1249A polymorphism on the risk of resistance to antiepileptic drugs: a meta-analysis of the literature.
    Genetic testing and molecular biomarkers, 2014, Volume: 18, Issue:2

    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

Other Studies

9 other study(ies) available for isoleucine and Epilepsy

ArticleYear
Insights into the development of pentylenetetrazole-induced epileptic seizures from dynamic metabolomic changes.
    Metabolic brain disease, 2022, Volume: 37, Issue:7

    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.
    Metabolic brain disease, 2017, Volume: 32, Issue:6

    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.
    Epilepsy research, 2007, Volume: 75, Issue:1

    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.
    Developmental medicine and child neurology, 1967, Volume: 9, Issue:2

    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.
    Neurochemical research, 1980, Volume: 5, Issue:6

    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.
    Therapeutic drug monitoring, 2000, Volume: 22, Issue:3

    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.
    European journal of pediatrics, 1987, Volume: 146, Issue:4

    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.
    Archives of neurology, 1973, Volume: 28, Issue:3

    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.
    Journal of mental deficiency research, 1973, Volume: 17, Issue:2

    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