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Arginosuccinic aciduria

Known as: arginosuccinate lyase deficiency 
 
National Institutes of Health

Related topics

Related topics

4 relations

Broader (3)

Argininosuccinic AciduriaEnzyme DeficiencyUrea Cycle Disorders, Inborn
autosomal recessive trait

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Early liver transplantation in neonatal-onset and moderate urea cycle disorders may lead to normal neurodevelopment
Urea cycle disorders (UCDs) are inherited metabolic diseases that lead to hyperammonemia. Neurodevelopmental outcomes of patients… Expand
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Review
2016
Review
2016
Continuous Renal Replacement Therapy in NICU — Indian Experience
To the Editor : Continuous renal replacement therapy (CRRT) is an extracorporeal blood purification therapy intended to… Expand
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Highly Cited
2001
Highly Cited
2001
Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program.
BACKGROUND Tandem mass spectrometry (MS/MS) is rapidly being adopted by newborn screening programs to screen dried blood spots… Expand
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1981
1981
Neonatal arginosuccinic aciduria.
 
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