isomethyleugenol has been researched along with Amino Acid Metabolism Disorders, Inborn in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (15.38) | 18.7374 |
| 1990's | 3 (23.08) | 18.2507 |
| 2000's | 2 (15.38) | 29.6817 |
| 2010's | 5 (38.46) | 24.3611 |
| 2020's | 1 (7.69) | 2.80 |
| Authors | Studies |
|---|---|
| Bouvier, D; Brailova, M; Minet-Quinard, R; Regnier, A; Sapin, V; Szymanowski, M | 1 |
| Baethmann, M; Ballhausen, D; Baumgartner, MR; Blasco-Alonso, J; Blom, H; Boy, N; Bueno, M; Burgos Peláez, R; Cerone, R; Chabrol, B; Chapman, KA; Couce, ML; Crushell, E; Dalmau Serra, J; Diodato, D; Diogo, L; Dionisi-Vici, C; Ficicioglu, C; Froese, DS; García Jimenez, MC; García Silva, MT; Gaspar, AM; Gautschi, M; Gleich, F; González-Lamuño, D; Gouveia, S; Grünewald, S; Hendriksz, C; Huemer, M; Janssen, MCH; Jesina, P; Koch, J; Kölker, S; Konstantopoulou, V; Kožich, V; Lavigne, C; Lund, AM; Martin, CA; Martinelli, D; Martins, EG; Meavilla Olivas, S; Mention, K; Mochel, F; Morris, AA; Mundy, H; Murphy, E; Olivieri, G; Paquay, S; Pedrón-Giner, C; Ruiz Gómez, MA; Santra, S; Schiff, M; Scholl-Bürgi, S; Schwartz, IV; Seifert, B; Servais, A; Skouma, A; Tran, C; Vives Piñera, I; Walter, J; Weisfeld-Adams, J | 1 |
| Carrasco, M; Castro, C; Lu, SC; Luka, Z; Martínez-Chantar, ML; Mato, JM; Micó, JA; Murillo-Carretero, M; Ortega-Martínez, S; Rabaneda, LG; Wagner, C; Woodhoo, A | 1 |
| Augoustides-Savvopoulou, P; Baumgartner, MR; Blair, E; Brennerova, K; Broomfield, A; Bürer, C; De Meirleir, L; Fowler, B; Gökcay, G; Hennermann, J; Huemer, M; Jardine, P; Ješina, P; Koch, J; Kožich, V; Landolt, MA; Lorenzl, S; Lotz-Havla, AS; Noss, J; Parini, R; Peters, H; Plecko, B; Ramos, FJ; Schlune, A; Suormala, T; Tsiakas, K; Zerjav Tansek, M | 1 |
| Cheillan, D; Dessein, AF; Dobbelaere, D; Fontaine, M; Joncquel-Chevalier Curt, M; Mention-Mulliez, K; Porchet, N; Soto-Ares, G; Vamecq, J; Voicu, PM | 1 |
| Ataullakhanov, FI; Banerjee, R; Martinov, MV; Vitvitsky, VM | 1 |
| Lawson-Yuen, A; Levy, HL | 1 |
| Magee, PN; Nyce, J; Weinhouse, S | 1 |
| Rees, MM; Rodgers, GM | 1 |
| Bottiglieri, T; Charles, HC; Gray, L; Hyland, K; Jaeken, J; Kahler, SG; Lazeyras, F; Van Hove, JL; Zeisel, SH | 1 |
| Bräutigam, C; Hoffman, GF; Hyland, K; Knust, A; Sharma, RK; Wevers, RA | 1 |
| Miller, JW; Selhub, J | 1 |
| Benjafield, JG; Rutter, LF | 1 |
6 review(s) available for isomethyleugenol and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
Creatine biosynthesis and transport in health and disease.
Topics: Amidinotransferases; Amino Acid Metabolism, Inborn Errors; Amino Acid Transport Systems, Basic; AMP-Activated Protein Kinases; Animals; Biological Transport, Active; Brain Diseases, Metabolic, Inborn; Creatine; Developmental Disabilities; Energy Metabolism; Guanidinoacetate N-Methyltransferase; Gyrate Atrophy; Humans; Hyperammonemia; Intellectual Disability; Language Development Disorders; Mental Retardation, X-Linked; Methylation; Mitochondrial Membrane Transport Proteins; Movement Disorders; Mutation; Nerve Tissue Proteins; Ornithine; Plasma Membrane Neurotransmitter Transport Proteins; Prenatal Diagnosis; S-Adenosylmethionine; Speech Disorders; Urea Cycle Disorders, Inborn | 2015 |
The logic of the hepatic methionine metabolic cycle.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Glycine N-Methyltransferase; Humans; Liver; Metabolic Networks and Pathways; Methionine; Methionine Adenosyltransferase; Methylation; Methyltransferases; Models, Biological; S-Adenosylmethionine | 2010 |
The use of betaine in the treatment of elevated homocysteine.
Topics: Amino Acid Metabolism, Inborn Errors; Betaine; Homocysteine; Homocystinuria; Humans; Hyperhomocysteinemia; Methionine; Methylation | 2006 |
5-Methylcytosine depletion during tumour development: an extension of the miscoding concept.
Topics: 5-Methylcytosine; Alkylation; Amino Acid Metabolism, Inborn Errors; Animals; Carcinogens; Cell Transformation, Neoplastic; Choline Deficiency; Cytosine; DNA; DNA Repair; Gene Expression Regulation; Humans; Methylation; Methyltransferases; Models, Genetic; Neoplasms; Oncogenes; Rats; Tyrosine; Vitamin B 6 Deficiency | 1983 |
Homocysteinemia: association of a metabolic disorder with vascular disease and thrombosis.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Blood Coagulation Factors; Blood Platelets; Child; Cystathionine beta-Synthase; Endothelium, Vascular; Fibrinolytic Agents; Folic Acid Deficiency; Homocysteine; Humans; Incidence; Male; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Penicillamine; Risk Factors; Thrombosis; Vascular Diseases; Vitamin B 12; Vitamin B 6 Deficiency; Vitamins | 1993 |
The pathogenesis of homocysteinemia: interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine.
Topics: Amino Acid Metabolism, Inborn Errors; Cystathionine; Homocysteine; Humans; Methionine; Methylation; S-Adenosylmethionine | 1992 |
7 other study(ies) available for isomethyleugenol and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
[Remethylation disorders: about two cases].
Topics: Alcoholism; Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Female; Folic Acid; Folic Acid Deficiency; Homocysteine; Homocystinuria; Humans; Infant, Newborn; Metabolic Networks and Pathways; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged; Muscle Spasticity; Psychotic Disorders; Vitamin B 12 | 2020 |
Phenotype, treatment practice and outcome in the cobalamin-dependent remethylation disorders and MTHFR deficiency: Data from the E-HOD registry.
Topics: Adolescent; Adult; Age of Onset; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Cross-Sectional Studies; Disease Progression; Europe; Female; Homocystinuria; Humans; Infant; Infant, Newborn; Male; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Methylmalonic Acid; Muscle Spasticity; Phenotype; Pregnancy; Psychotic Disorders; Registries; Retrospective Studies; Vitamin B 12; Young Adult | 2019 |
Glycine N-methyltransferase expression in the hippocampus and its role in neurogenesis and cognitive performance.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Cognition; Cyclin E; Fibroblast Growth Factor 2; Gene Expression Regulation; Glycine N-Methyltransferase; Hippocampus; MAP Kinase Signaling System; Maze Learning; Memory Disorders; Methionine; Methionine Adenosyltransferase; Methylation; Mice; Mice, Inbred C57BL; Mice, Knockout; Nerve Tissue Proteins; Neurogenesis; Neuronal Plasticity; Rotarod Performance Test; S-Adenosylmethionine | 2014 |
Clinical onset and course, response to treatment and outcome in 24 patients with the cblE or cblG remethylation defect complemented by genetic and in vitro enzyme study data.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adolescent; Age of Onset; Amino Acid Metabolism, Inborn Errors; Cells, Cultured; Child; Child, Preschool; Disease Progression; Female; Ferredoxin-NADP Reductase; Humans; Infant; Infant, Newborn; Male; Methylation; Pregnancy; Retrospective Studies; Treatment Outcome; Vitamin B 12; Young Adult | 2015 |
One-methyl group metabolism in non-ketotic hyperglycinaemia: mildly elevated cerebrospinal fluid homocysteine levels.
Topics: Amino Acid Metabolism, Inborn Errors; Benzoic Acid; Brain Diseases; Choline; Coma; Female; Glycine; Homocysteine; Humans; Infant; Infant, Newborn; Male; Methionine; Methylation; Phosphatidylcholines; S-Adenosylmethionine; Seizures; Serine; Tetrahydrofolates | 1998 |
The influence of L-dopa on methylation capacity in aromatic L-amino acid decarboxylase deficiency: biochemical findings in two patients.
Topics: Amino Acid Metabolism, Inborn Errors; Aromatic-L-Amino-Acid Decarboxylases; Dopamine; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Hypokinesia; Levodopa; Methoxyhydroxyphenylglycol; Methylation; Muscle Hypotonia; Tetrahydrofolates; Tyrosine | 2000 |
Significance of metabolic disorders in schizophrenia.
Topics: Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Dopamine; Female; Humans; Male; Methylation; Schizophrenia; Tyrosine | 1973 |