Nonketotic Hyperglycinemia

Known as: Hyperglycinemia, Nonketotic, Glycine Encephalopathies, Hyperglycinemia, Nonketotic [Disease/Finding] 
An autosomal recessive metabolic disorder caused by mutations in the AMT and GLDC genes. It is characterized by abnormal accumulation of glycine in… (More)
National Institutes of Health

Papers overview

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Review
2017
Review
2017
Chlorogenic acid (CGA), an important biologically active dietary polyphenol, is produced by certain plant species and is a major… (More)
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2015
2015
UNLABELLED To present three cases who presented with neonatal hiccups and who were later diagnosed with nonketotic… (More)
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Highly Cited
2009
Highly Cited
2009
A general framework based on histogram equalization for image contrast enhancement is presented. In this framework, contrast… (More)
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2009
2009
Nonketotic hyperglycinemia is an autosomal recessive disorder of glycine metabolism. Patients generally present in the neonatal… (More)
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Review
2008
Review
2008
The glycine cleavage system catalyzes the following reversible reaction: Glycine + H(4)folate + NAD(+) <==> 5,10-methylene-H(4… (More)
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2006
2006
Serial diffusion-weighted (DWI) and diffusion tensor imaging (DTI) were performed in a patient with neonatal onset nonketotic… (More)
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Review
2001
Review
2001
Nonketotic hyperglycinemia (NKH) is an autosomal recessive disorder of glycine metabolism caused by a defect in the glycine… (More)
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2000
2000
We present four patients with typical neonatal onset non-ketotic hyperglycinemia (NKH) who developed hydrocephalus requiring… (More)
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1989
1989
MR imaging in seven patients (4 days to 38 months old) with nonketotic hyperglycinemia showed age-related findings of progressive… (More)
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1979
1979
Nonketotic hyperglycinemia is an inborn error of metabolism resulting from a defect in the glycine cleavage enzyme system. It is… (More)
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