sulfobromophthalein has been researched along with Galactosemias in 3 studies
Sulfobromophthalein: A phenolphthalein that is used as a diagnostic aid in hepatic function determination.
Galactosemias: A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)
| 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 |
|---|---|
| Gross, O | 1 |
| Audetat, V | 1 |
| Bircher, J | 1 |
| Colón, AR | 1 |
| Sandberg, DH | 1 |
| Lüders, D | 1 |
2 reviews available for sulfobromophthalein and Galactosemias
| Article | Year |
|---|---|
Presently recognized forms of inherited jaundice in infancy. A summary and review.
Topics: Bilirubin; Biological Transport; Cholestasis; Diagnosis, Differential; Feces; Galactosemias; Hepatit | 1973 |
[Neonatal hepatitis and bile duct atresia].
Topics: Bile Ducts; Bilirubin; Cholestasis; Congenital Abnormalities; Diagnosis, Differential; Feces; Galact | 1974 |
1 other study available for sulfobromophthalein and Galactosemias
| Article | Year |
|---|---|
[Blood cholinesterase and hepatic function: a comparison with BSP and galactose elimination as well as serum albumin concentration].
Topics: Adult; Aged; Cholinesterases; Female; Galactosemias; Humans; Liver; Liver Diseases; Liver Function T | 1978 |