catechol has been researched along with Hypoadrenocorticism, Familial in 1 studies
Hypoadrenocorticism, Familial: Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (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 |
|---|---|
| LUFT, R | 1 |
| VON EULER, US | 1 |
1 other study available for catechol and Hypoadrenocorticism, Familial
| Article | Year |
|---|---|
Urinary excretion of catechol amines during insulin hypoglycemia in five patients with Addison's disease and in one patient after bilateral adrenalectomy.
Topics: Addison Disease; Adrenal Insufficiency; Adrenalectomy; Amines; Catechols; Epinephrine; Humans; Hyper | 1957 |