phytanic acid has been researched along with alpha-Galactosidase A Deficiency in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (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 |
|---|---|
| Asbury, AK; Braine, H; Moser, HW; Murray, C; Pyeritz, RE; Ullman, D | 1 |
| Batshaw, ML; Braine, H; Brusilow, SW; Moser, HW; Murray, C | 1 |
| Thomas, PK | 1 |
1 review(s) available for phytanic acid and alpha-Galactosidase A Deficiency
| Article | Year |
|---|---|
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 |
2 other study(ies) available for phytanic acid and alpha-Galactosidase A Deficiency
| Article | Year |
|---|---|
Therapeutic trial of plasmapheresis in Refsum disease and in Fabry disease.
Topics: Adult; Fabry Disease; Female; Glycosphingolipids; Humans; Male; Phytanic Acid; Plasmapheresis; Refsum Disease | 1980 |
Management of heritable disorders of the urea cycle and of Refsum's and Fabry's diseases.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Arginine; Benzoates; Carbamoyl-Phosphate Synthase (Ammonia); Dietary Proteins; Fabry Disease; Hippurates; Humans; Male; Nitrogen; Ornithine Carbamoyltransferase Deficiency Disease; Phytanic Acid; Plasmapheresis; Refsum Disease; Trihexosylceramides; Urea | 1979 |