aminolevulinic acid has been researched along with Syndrome in 6 studies
Aminolevulinic Acid: A compound produced from succinyl-CoA and GLYCINE as an intermediate in heme synthesis. It is used as a PHOTOCHEMOTHERAPY for actinic KERATOSIS.
5-aminolevulinic acid : The simplest delta-amino acid in which the hydrogens at the gamma position are replaced by an oxo group. It is metabolised to protoporphyrin IX, a photoactive compound which accumulates in the skin. Used (in the form of the hydrochloride salt)in combination with blue light illumination for the treatment of minimally to moderately thick actinic keratosis of the face or scalp.
Syndrome: A characteristic symptom complex.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 5 (83.33) | 18.7374 |
1990's | 1 (16.67) | 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 |
---|---|
Chalmers, RA | 1 |
Lawson, AM | 1 |
Watts, RW | 1 |
Tavill, AS | 1 |
Kamerling, JP | 1 |
Hey, E | 1 |
Ogilvie, D | 1 |
O'Connor, LJ | 1 |
Pisanets, M | 1 |
Poriazov, K | 1 |
Doss, M | 1 |
von Tiepermann, R | 1 |
Schneider, J | 1 |
Nordmann, Y | 1 |
Amram, D | 1 |
Deybach, JC | 1 |
Phung, LN | 1 |
Lesbros, D | 1 |
Rapaccini, GL | 1 |
Topi, GC | 1 |
Anti, M | 1 |
D'Alessandro Gandolfo, L | 1 |
Griso, D | 1 |
Amantea, A | 1 |
de Vitis, I | 1 |
Fedeli, G | 1 |
6 other studies available for aminolevulinic acid and Syndrome
Article | Year |
---|---|
D-2-hydroxyglutaric aciduria: case report and biochemical studies.
Topics: Aminolevulinic Acid; Asthma; Child, Preschool; Chromatography, Gas; Chromatography, Ion Exchange; Fo | 1980 |
Acute intermittent porphyria.
Topics: Acute Disease; Adult; Aminolevulinic Acid; Female; Humans; Male; Porphobilinogen; Porphyrias; Seizur | 1981 |
[Porphyrin biosynthesis in parturients with the EPH syndrome and their newborn infants].
Topics: Adolescent; Adult; Aminolevulinic Acid; Erythrocytes; Female; Hemoglobins; Humans; In Vitro Techniqu | 1982 |
Acute hepatic porphyria syndrome with porphobilinogen synthase defect.
Topics: Acute Disease; Adult; Amino Acids; Aminolevulinic Acid; Erythrocytes; Feces; Female; Humans; Lead; L | 1980 |
Coexistent hereditary coproporphyria and congenital erythropoietic porphyria (Günther disease).
Topics: Aging; Aminolevulinic Acid; Coproporphyrins; Erythrocytes; Feces; Female; Hemolysis; Humans; Infant; | 1990 |
Porphyrins in Rotor's syndrome: a study on an Italian family.
Topics: Adult; Aminolevulinic Acid; Coproporphyrins; Female; Humans; Jaundice; Liver; Male; Porphobilinogen; | 1986 |