Congenital glucose-galactose malabsorption

Known as: Glucose-Galactose Malabsorption, Carbohydrate Intolerance, Glucose Galactose Malabsorption 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1974-2017
051019742017

Papers overview

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2012
2012
Glucose–galactose malabsorption (GGM) is an autosomal recessive disease caused by mutations in the Na+/glucose cotransporter gene… (More)
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2010
Highly Cited
2010
With the advent of high-throughput targeted metabolic profiling techniques, the question of how to interpret and analyze the… (More)
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2009
Highly Cited
2009
Biological networks characterize the interactions of biomolecules at a systems-level. One important property of biological… (More)
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2007
Highly Cited
2007
We describe a gene network for the Arabidopsis thaliana transcriptome based on a modified graphical Gaussian model (GGM). Through… (More)
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2005
Highly Cited
2005
There are two broad classes of models used to address the econometric problems caused by skewness in data commonly encountered in… (More)
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2003
2003
Glucose-galactose malabsorption (GGM) is a rare autosomal recessive disorder of intestinal transport of glucose and galactose… (More)
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2002
Highly Cited
2002
MOTIVATION Recent advances in DNA microarray technologies have made it possible to measure the expression levels of thousands of… (More)
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2002
2002
In a gauge theory of weak and associated interactions (electromagnetic, strong .... ) in which parity and time reversal are… (More)
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2001
2001
Introduction Congenital glucose galactose malabsorption (CGGM) is a rare autosomal recessive disorder, which presents as a… (More)
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1991
Highly Cited
1991
Glucose/galactose malabsorption (GGM) is an autosomal recessive disease manifesting within the first weeks of life and… (More)
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