Page last updated: 2024-10-17

creatine and Galactosemias

creatine has been researched along with Galactosemias in 1 studies

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)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19901 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
COTLIER, E1

Other Studies

1 other study available for creatine and Galactosemias

ArticleYear
SYNTHESIS OF CREATINE PHOSPHATE BY THE CRYSTALLINE LENS; IN NORMAL CONDITIONS AND DURING THE DEVELOPMENT OF GALACTOSE CATARACT.
    American journal of ophthalmology, 1964, Volume: 57

    Topics: Adenosine Triphosphate; Cataract; Coenzymes; Creatine; Creatinine; Eye Proteins; Galactose; Galactos

1964