hexacosanoic acid has been researched along with Symptom Cluster in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Benke, PJ; Brown, FR; Kelley, RI; Moser, AE; Moser, HW; Singh, I; Solish, GI | 1 |
Bakkeren, JA; Maas, JM; Monnens, LA; Trijbels, JM | 1 |
Kawamura, N; Kishimoto, Y; Moser, AB; Moser, HW; Murphy, J; Schaumburg, H; Suzuki, K | 1 |
Nijenhuis, A; Schutgens, RB; Tager, JM; Tromp, A; van den Bosch, H; van Roermund, CW; van Wijland, MJ; Wanders, RJ | 1 |
Heikoop, J; Schram, AW; Schutgens, RB; Tager, JM; van den Bosch, H; van Roermund, CW; van Wijland, MJ; Wanders, RJ | 1 |
5 other study(ies) available for hexacosanoic acid and Symptom Cluster
Article | Year |
---|---|
The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis.
Topics: Abnormalities, Multiple; Adrenoleukodystrophy; Amniocentesis; Brain Diseases; Diagnosis, Differential; Fatty Acids; Fatty Acids, Monounsaturated; Fatty Acids, Unsaturated; Female; Fibroblasts; Humans; Kidney Diseases, Cystic; Liver Diseases; Male; Microbodies; Pregnancy; Prenatal Diagnosis; Syndrome | 1984 |
Serum very long chain fatty acid pattern in Zellweger syndrome.
Topics: Adult; Brain Diseases; Child; Chromatography, Gas; Fatty Acids; Female; Humans; Kidney Diseases; Liver Diseases; Male; Microbodies; Molecular Weight; Syndrome | 1984 |
Adrenoleukodystrophy: elevated C26 fatty acid in cultured skin fibroblasts.
Topics: Adolescent; Adrenal Insufficiency; Adult; Cells, Cultured; Child; Diffuse Cerebral Sclerosis of Schilder; Fatty Acids; Female; Fibroblasts; Genetic Carrier Screening; Humans; Male; Middle Aged; Skin; Syndrome | 1980 |
Prenatal diagnosis of Zellweger syndrome by measurement of very long chain fatty acid (C26:0) beta-oxidation in cultured chorionic villous fibroblasts: implications for early diagnosis of other peroxisomal disorders.
Topics: Cells, Cultured; Fatty Acids; Female; Fetal Diseases; Fibroblasts; Humans; Microbodies; Oxidation-Reduction; Pregnancy; Prenatal Diagnosis; Syndrome | 1987 |
Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders.
Topics: Facial Bones; Fatty Acids; Hepatomegaly; Humans; Microbodies; Oxidation-Reduction; Palmitates; Polycystic Kidney Diseases; Skin; Skull; Syndrome | 1987 |