isomethyleugenol has been researched along with Inborn Errors of Metabolism in 19 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (36.84) | 18.7374 |
| 1990's | 7 (36.84) | 18.2507 |
| 2000's | 2 (10.53) | 29.6817 |
| 2010's | 2 (10.53) | 24.3611 |
| 2020's | 1 (5.26) | 2.80 |
| Authors | Studies |
|---|---|
| Kožich, V; Stabler, S | 1 |
| Augoustides-Savvopoulou, P; Barić, I; Blom, HJ; Chien, YH; Dobbelaere, D; Grünert, SC; Opladen, T; Petković Ramadža, D; Rakić, B; Staufner, C; Wedell, A | 1 |
| Benoist, JF; Giraudier, S; Ogier de Baulny, H; Royer, N; Schiff, M; Tilea, B | 1 |
| Busby, MG; da Costa, KA; Fischer, L; Mar, MH; Thompson, D; Zeisel, SH | 1 |
| Fontaine, B; Lyon-Caen, O; Saudubray, JM; Sedel, F | 1 |
| Bottiglieri, T; Hyland, K; Reynolds, EH | 1 |
| Ballabriga, A; Martinez, M; Mougan, I; Roig, M | 1 |
| Surtees, R | 2 |
| Gérard, M; Ogier de Baulny, H; Saudubray, JM; Zittoun, J | 1 |
| Al Essa, M; Al Jishi, EA; Dabbagh, O; Joshi, S; Ozand, PT; Powe, JE; Rashed, MS; Sakati, NA | 1 |
| Hoffmann, GF; Surtees, RA; Wevers, RA | 1 |
| Mudd, SH | 1 |
| Freeman, JM; Mudd, SH | 1 |
| King, JO; Levine, SP; Markey, SP; Witten, TA | 1 |
| Ando, T; Cottom, D; Hull, D; Kilroy, AW; Nyhan, WL; Rasmussen, K; Wadlington, W | 1 |
| Mahoney, MJ; Mudd, SH; Rosenberg, LE; Uhlendorf, BW | 1 |
| Goodman, SI; Hammond, KB | 1 |
| Taborsky, RG | 1 |
10 review(s) available for isomethyleugenol and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Lessons Learned from Inherited Metabolic Disorders of Sulfur-Containing Amino Acids Metabolism.
Topics: Amino Acids, Sulfur; Animals; Brain Diseases; Cysteine; Glutathione; Homocysteine; Homocystinuria; Humans; Hydrogen Sulfide; Liver; Metabolic Diseases; Metabolism, Inborn Errors; Methionine; Methionine Adenosyltransferase; Methylation; S-Adenosylmethionine; Sulfites; Sulfur; Sulfur Compounds | 2020 |
Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders.
Topics: Consensus; Homocysteine; Humans; Infant, Newborn; Metabolism, Inborn Errors; Methionine; Methionine Adenosyltransferase; Methylation; Neonatal Screening; S-Adenosylhomocysteine; S-Adenosylmethionine | 2017 |
Isolated remethylation disorders: do our treatments benefit patients?
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adolescent; Adult; Ferredoxin-NADP Reductase; Homocystinuria; Humans; Infant, Newborn; Metabolism, Inborn Errors; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Models, Biological; Muscle Spasticity; Psychotic Disorders; Risk Assessment | 2011 |
Hereditary spastic paraparesis in adults associated with inborn errors of metabolism: a diagnostic approach.
Topics: Age of Onset; Decision Trees; Female; Genetic Diseases, Inborn; Humans; Male; Metabolism, Inborn Errors; Methylation; Motor Neurons; Paraparesis, Spastic; Spinal Cord; Syndrome | 2007 |
The clinical potential of ademetionine (S-adenosylmethionine) in neurological disorders.
Topics: AIDS Dementia Complex; Animals; Brain Diseases; Dementia; Disease Models, Animal; Epilepsy; Humans; Metabolism, Inborn Errors; Methotrexate; Methylation; Multiple Sclerosis; Neurotransmitter Agents; Parkinson Disease; Receptors, Neurotransmitter; S-Adenosylmethionine; Spinal Cord Diseases | 1994 |
Biochemical pathogenesis of subacute combined degeneration of the spinal cord and brain.
Topics: Brain Diseases; Demyelinating Diseases; Humans; Metabolism, Inborn Errors; Methylation; Nerve Degeneration; Spinal Cord Diseases; Vitamin B 12; Vitamin B 12 Deficiency | 1993 |
Remethylation defects: guidelines for clinical diagnosis and treatment.
Topics: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase; Adult; Betaine; Child, Preschool; Folic Acid; Homocysteine; Humans; Hydroxocobalamin; Infant; Infant, Newborn; Metabolism, Inborn Errors; Methionine; Methylation; Methylenetetrahydrofolate Reductase (NADPH2); Methylmalonic Acid; Oxidoreductases Acting on CH-NH Group Donors; Practice Guidelines as Topic; Vitamin B 12 | 1998 |
Demyelination and inborn errors of the single carbon transfer pathway.
Topics: Demyelinating Diseases; Humans; Liver; Metabolism, Inborn Errors; Methionine Adenosyltransferase; Methylation; Myelin Basic Protein; One-Carbon Group Transferases; S-Adenosylmethionine | 1998 |
Cerebrospinal fluid investigations for neurometabolic disorders.
Topics: Adolescent; Biogenic Monoamines; Biomarkers; Brain Diseases, Metabolic; Child; Child, Preschool; Clinical Protocols; Disease Progression; Female; gamma-Aminobutyric Acid; Gene Expression; Humans; Infant; Infant, Newborn; Male; Metabolism, Inborn Errors; Methylation | 1998 |
Diseases of sulphur metabolism: implications for the methionine-homocysteine cycle, and vitamin responsiveness.
Topics: Adolescent; Cystathionine beta-Synthase; Homocysteine; Homocystinuria; Humans; Metabolism, Inborn Errors; Methionine; Methylation; Pyridoxine; Sulfur | 1979 |
9 other study(ies) available for isomethyleugenol and Inborn Errors of Metabolism
| Article | Year |
|---|---|
Choline- and betaine-defined diets for use in clinical research and for the management of trimethylaminuria.
Topics: Betaine; Choline; Dietary Supplements; Dietetics; Dose-Response Relationship, Drug; Food Analysis; Humans; Metabolism, Inborn Errors; Methylamines; Methylation; Nutrition Policy; Nutritional Requirements; Practice Guidelines as Topic | 2004 |
Blood polyunsaturated fatty acids in patients with peroxisomal disorders. A multicenter study.
Topics: Adolescent; Adrenoleukodystrophy; Adult; Arachidonic Acid; Child; Child, Preschool; Docosahexaenoic Acids; Erythrocytes; Fatty Acids, Unsaturated; Humans; Infant; Linoleic Acid; Linoleic Acids; Metabolism, Inborn Errors; Methylation; Microbodies; Plasmalogens; X Chromosome | 1994 |
Inborn error of vitamin B12 metabolism: a treatable cause of childhood dementia/paralysis.
Topics: Age of Onset; Anemia, Hemolytic; Anemia, Megaloblastic; Blood Transfusion; Child; Child, Preschool; Dementia; Demyelinating Diseases; Diagnostic Errors; Family Health; Female; Gas Chromatography-Mass Spectrometry; Humans; Hydroxocobalamin; Metabolism, Inborn Errors; Methylation; Nuclear Family; Paralysis; Vitamin B 12 Deficiency | 1998 |
N-5,10-methylenetetrahydrofolate reductase deficiency and schizophrenia: a working hypothesis.
Topics: Adolescent; Dopamine; Female; Fibroblasts; Folic Acid; Homocysteine; Humans; Male; Metabolism, Inborn Errors; Methylation; Methylenetetrahydrofolate Dehydrogenase (NADP); Methyltransferases; Oxidoreductases; Schizophrenia; Tetrahydrofolates | 1974 |
Gas-chromatographic-mass-spectrometric determination of urinary acid profiles of normal young adults on a controlled diet.
Topics: Acetamides; Adult; Carboxylic Acids; Chromatography; Chromatography, Gas; Creatinine; Dicarboxylic Acids; Diet; Evaluation Studies as Topic; Fasting; Female; Fluoroacetates; Humans; Hydroxybutyrates; Male; Malonates; Mass Spectrometry; Metabolism, Inborn Errors; Methylation; Nutritional Physiological Phenomena; Phenylacetates; Silicon | 1973 |
Excretion of tiglylglycine in propionic acidemia.
Topics: Butyrates; Cells, Cultured; Chromatography, Gas; Coenzyme A; Diet Therapy; Fibroblasts; Glycine; Humans; Ligases; Mass Spectrometry; Metabolism, Inborn Errors; Methylation; Propionates | 1972 |
Defective metabolism of vitamin B 12 in fibroblasts from children with methylmalonicaciduria.
Topics: Adolescent; Adult; Cells, Cultured; Child; Child, Preschool; Cobalt Isotopes; Deoxyadenosines; Enzyme Activation; Fibroblasts; Folic Acid; Homocysteine; Humans; Hydroxocobalamin; Infant; Infant, Newborn; Male; Malonates; Metabolism, Inborn Errors; Methylation; Methyltransferases; Vitamin B 12 | 1971 |
A gas chromatographic procedure for detection of pathological organic aciduria.
Topics: Acetates; Acids; Butyrates; Caproates; Chromatography, Gas; Dicarboxylic Acids; Glycols; Humans; Infant, Newborn; Lactates; Malonates; Metabolism, Inborn Errors; Methods; Methylation; Propionates; Solvents; Succinates; Valerates | 1970 |
Indoxyl derivatives: potential psychotropic metabolites.
Topics: Adrenochrome; Animals; Behavior, Animal; Diseases in Twins; Ethanol; Humans; Indoles; Male; Metabolism, Inborn Errors; Methylation; Psychoses, Substance-Induced; Rats; Reward | 1968 |