I describe a rapid quantitative centrifugal analysis for galactose in blood. The technique involves galactose de-hydrogenase. As compared to the manual (o..toluidine) method for galactose determination, analysis time (4 mm 45 s on the GEMSAEC, 4 mm io s on the CentrifiChem) and sample volume (5 gil) were considerably reduced. Sample deproteinization is eliminated. A modified com-mercial kit was also tested. Results by the procedure correlate well with those by the more classical methods and analytical recovery is about 100%. The method is applied to the determination of galactose in intravenous galactose tolerance tests. Results of actual tests are re-ported. Additional Keyphrases: galactose dehydrogenase pseudo-end-point analysis GEMSAEC a...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
Galactosemia, caused by an hereditary deficiency (1) of galactose-1-phosphate uridyltransferase (EC ...
A modification of the orcinol procedure of Bruckner has been developed to permit rapid analysis of g...
The blood galactose concentration was assayed by a galactose oxidase method and intravenous galactos...
An inexpensive automated fluorometric technique for blood galactose determination has been modified ...
The blood galactose concentration was assayed by a galactose oxidase method and intravenous galactos...
The quantitative measurement of galactose in blood is essential for the early diagnosis, treatment, ...
A new glucose dehydrogenase preparation has been used to determine the glucose concentration in seru...
The manual fluorimetric procedure, considered as a reference method for the determination of N-acety...
from the blood depends on nutrient hepatic blood flow. We can measure such concentrations, which was...
Reportedly, galactose provides an alternative carbohydrate source and improved homeostatic regulatio...
Background: Classical galactosaemia (OMIM #230400) is a rare disorder of carbohydrate metabolism cau...
Background: Classical galactosaemia (OMIM #230400) is a rare disorder of carbohydrate metabolism cau...
A screeningprocedure is described which can be used to separate the great majority of normal persons...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
Galactosemia, caused by an hereditary deficiency (1) of galactose-1-phosphate uridyltransferase (EC ...
A modification of the orcinol procedure of Bruckner has been developed to permit rapid analysis of g...
The blood galactose concentration was assayed by a galactose oxidase method and intravenous galactos...
An inexpensive automated fluorometric technique for blood galactose determination has been modified ...
The blood galactose concentration was assayed by a galactose oxidase method and intravenous galactos...
The quantitative measurement of galactose in blood is essential for the early diagnosis, treatment, ...
A new glucose dehydrogenase preparation has been used to determine the glucose concentration in seru...
The manual fluorimetric procedure, considered as a reference method for the determination of N-acety...
from the blood depends on nutrient hepatic blood flow. We can measure such concentrations, which was...
Reportedly, galactose provides an alternative carbohydrate source and improved homeostatic regulatio...
Background: Classical galactosaemia (OMIM #230400) is a rare disorder of carbohydrate metabolism cau...
Background: Classical galactosaemia (OMIM #230400) is a rare disorder of carbohydrate metabolism cau...
A screeningprocedure is described which can be used to separate the great majority of normal persons...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
Galactosemia, caused by an hereditary deficiency (1) of galactose-1-phosphate uridyltransferase (EC ...