1-anilino-8-naphthalenesulfonate has been researched along with Porphyrias in 3 studies
1-anilino-8-naphthalenesulfonate: RN given refers to parent cpd
8-anilinonaphthalene-1-sulfonic acid : A naphthalenesulfonic acid that is naphthalene-1-sulfonic acid substituted by a phenylamino group at position 8.
Porphyrias: A diverse group of metabolic diseases characterized by errors in the biosynthetic pathway of HEME in the LIVER, the BONE MARROW, or both. They are classified by the deficiency of specific enzymes, the tissue site of enzyme defect, or the clinical features that include neurological (acute) or cutaneous (skin lesions). Porphyrias can be hereditary or acquired as a result of toxicity to the hepatic or erythropoietic marrow tissues.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fernández-Miranda, C | 1 |
| De La Calle, M | 1 |
| Larumbe, S | 1 |
| Gómez-Izquierdo, T | 1 |
| Porres, A | 1 |
| Gómez-Gerique, J | 1 |
| Enríquez de Salamanca, R | 1 |
| Glencross, PM | 1 |
| Ledingham, DD | 1 |
| Alexander, JA | 1 |
| Pirozhenko, LS | 1 |
3 other studies available for 1-anilino-8-naphthalenesulfonate and Porphyrias
| Article | Year |
|---|---|
Lipoprotein abnormalities in patients with asymptomatic acute porphyria.
Topics: Acute Disease; Adult; Apolipoprotein A-I; Apolipoproteins B; Cholesterol; Cholesterol, HDL; Choleste | 2000 |
Acute porphyria presenting with hyperamylasemia.
Topics: Acute Disease; Adult; Amylases; Diagnosis, Differential; Female; Humans; Lipase; Pancreatitis; Porph | 1991 |
[Functional state of the stomach and the pancreas in patients with late skin porphyria].
Topics: Adult; Duodenum; Female; Humans; Lipase; Male; Middle Aged; Pancreas; Porphyrias; Stomach | 1973 |