phytanic acid has been researched along with Lipid Metabolism, Inborn Error in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 7 (77.78) | 18.7374 |
| 1990's | 1 (11.11) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Freeman, WD; Gavrilov, DK; Matern, D; Oglesbee, D; Smith, EH; Tortorelli, S; Vavra, MW | 1 |
| AVIGAN, J; BAXTER, J; MIZE, C; STEINBERG, D | 1 |
| Christensen, E; Jakobs, C; Largillière, C; ten Brink, HJ; van den Heuvel, CM | 1 |
| Høie, K; Skjeldal, OH; Stokke, O | 1 |
| Thomas, PK | 1 |
| Hall, NA; Hjelm, NM; Lynes, GW | 1 |
| Bernheimer, H; Kainz-Korschinsky, M; Molzer, B; Sundt-Heller, R | 1 |
| Cooper, K; Tsai, MY | 1 |
2 review(s) available for phytanic acid and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Disorders related to the metabolism of phytanic acid.
Topics: Animals; Eicosanoic Acids; Humans; Lipid Metabolism, Inborn Errors; Liver; Microbodies; Mixed Function Oxygenases; Oxidoreductases; Phytanic Acid; Rats; Refsum Disease | 1986 |
Inherited neuropathies related to disorders of lipid metabolism.
Topics: Abetalipoproteinemia; Amidohydrolases; Ceramidases; Fabry Disease; Galactosylceramidase; Gangliosidoses; Gaucher Disease; Humans; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipid Metabolism, Inborn Errors; Lipoproteins; Nervous System Diseases; Niemann-Pick Diseases; Phytanic Acid; Refsum Disease; Sphingomyelin Phosphodiesterase; Sulfatases; Tangier Disease; Xanthomatosis | 1988 |
7 other study(ies) available for phytanic acid and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
An adult onset case of alpha-methyl-acyl-CoA racemase deficiency.
Topics: Age of Onset; Biomarkers; DNA Mutational Analysis; Fatty Acids; Genetic Predisposition to Disease; Homozygote; Humans; Leukoencephalopathies; Lipid Metabolism, Inborn Errors; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Nervous System Diseases; Phenotype; Phytanic Acid; Racemases and Epimerases; Remission Induction; Seizures; Treatment Outcome | 2010 |
PHYTANIC ACID FORMATION AND ACCUMULATION IN PHYTOL-FED RATS.
Topics: Alcohols; Carbon Dioxide; Fatty Acids; Feces; Intestines; Lipid Metabolism; Lipid Metabolism, Inborn Errors; Liver; Lymph; Phytanic Acid; Phytol; Rats; Refsum Disease; Research; Urine | 1965 |
Diagnosis of peroxisomal disorders by analysis of phytanic and pristanic acids in stored blood spots collected at neonatal screening.
Topics: Fatty Acids; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Microbodies; Neonatal Screening; Phytanic Acid | 1993 |
Discussion: lipid disorders.
Topics: Abetalipoproteinemia; Ataxia; Humans; Hypobetalipoproteinemias; Lipid Metabolism, Inborn Errors; Phytanic Acid; Refsum Disease | 1978 |
Ratios for very-long-chain fatty acids in plasma of subjects with peroxisomal disorders, as determined by HPLC and validated by gas chromatography-mass spectrometry.
Topics: Adolescent; Adrenoleukodystrophy; Adult; Aging; Child; Child, Preschool; Chromatography, High Pressure Liquid; Fatty Acids; Female; Gas Chromatography-Mass Spectrometry; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Microbodies; Middle Aged; Phytanic Acid; Reference Values; Refsum Disease; Syndrome | 1988 |
Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders.
Topics: Adrenal Glands; Adrenoleukodystrophy; Brain; Cholesterol Esters; Eicosanoic Acids; Fatty Acids; Humans; Kidney; Lipid Metabolism, Inborn Errors; Microbodies; Phytanic Acid; Refsum Disease; Zellweger Syndrome | 1989 |
Long-chain aliphatic fatty acids and phytanic acid simultaneously measured by dual-column capillary chromatography.
Topics: Chromatography, Gas; Eicosanoic Acids; Fatty Acids; Humans; Lipid Metabolism, Inborn Errors; Mass Spectrometry; Microbodies; Phytanic Acid | 1989 |