A modification of the orcinol procedure of Bruckner has been developed to permit rapid analysis of galactose in blood. The method is sensitive to increased amounts of galactose in blood filtrates, but accurate estimations of low concentrations are diffi-cult because of interfering substances. Calculation of results has been simplified by the use of constants. Their derivations are given. P REVId)US INVESTIGATION (bile in this hospital requiring repeated ga-lactose tolerance tests on a family with 3 galactosemic nmembers (6, 7) denmoimstrated the desirability of sinmplification or modification of the tests available for use in infants. We questioumed the possibility of variations iim the umormal galactose tolerance curve with age amid sug-ge...
Newborn screening for classical galactosemia in the Netherlands is performed by five laboratories an...
Newborn screening for classical galactosemia in the Netherlands is performed by five laboratories an...
Galactosemia, caused by an hereditary deficiency (1) of galactose-1-phosphate uridyltransferase (EC ...
I describe a rapid quantitative centrifugal analysis for galactose in blood. The technique involves ...
The blood galactose concentration was assayed by a galactose oxidase method and intravenous galactos...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
The blood galactose concentration was assayed by a galactose oxidase method and intravenous galactos...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
An inexpensive automated fluorometric technique for blood galactose determination has been modified ...
Reportedly, galactose provides an alternative carbohydrate source and improved homeostatic regulatio...
The quantitative measurement of galactose in blood is essential for the early diagnosis, treatment, ...
tive assay for newborn mass screening of galactosemia, but it is qualitative and relies on visual in...
A screeningprocedure is described which can be used to separate the great majority of normal persons...
from the blood depends on nutrient hepatic blood flow. We can measure such concentrations, which was...
Galactosemia is an autosomal recessive disorder, caused by an impaired galactose metabolism, resulti...
Newborn screening for classical galactosemia in the Netherlands is performed by five laboratories an...
Newborn screening for classical galactosemia in the Netherlands is performed by five laboratories an...
Galactosemia, caused by an hereditary deficiency (1) of galactose-1-phosphate uridyltransferase (EC ...
I describe a rapid quantitative centrifugal analysis for galactose in blood. The technique involves ...
The blood galactose concentration was assayed by a galactose oxidase method and intravenous galactos...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
The blood galactose concentration was assayed by a galactose oxidase method and intravenous galactos...
A method has been developed for detecting elevated levels of galactose and galactose-1-phosphate in ...
An inexpensive automated fluorometric technique for blood galactose determination has been modified ...
Reportedly, galactose provides an alternative carbohydrate source and improved homeostatic regulatio...
The quantitative measurement of galactose in blood is essential for the early diagnosis, treatment, ...
tive assay for newborn mass screening of galactosemia, but it is qualitative and relies on visual in...
A screeningprocedure is described which can be used to separate the great majority of normal persons...
from the blood depends on nutrient hepatic blood flow. We can measure such concentrations, which was...
Galactosemia is an autosomal recessive disorder, caused by an impaired galactose metabolism, resulti...
Newborn screening for classical galactosemia in the Netherlands is performed by five laboratories an...
Newborn screening for classical galactosemia in the Netherlands is performed by five laboratories an...
Galactosemia, caused by an hereditary deficiency (1) of galactose-1-phosphate uridyltransferase (EC ...