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arginosuccinate lyase deficiency
National Institutes of Health
Urea Cycle Disorders, Inborn
autosomal recessive trait
Semantic Scholar uses AI to extract papers important to this topic.
Early liver transplantation in neonatal-onset and moderate urea cycle disorders may lead to normal neurodevelopment
Metabolic Brain Disease
Corpus ID: 47020054
Urea cycle disorders (UCDs) are inherited metabolic diseases that lead to hyperammonemia. Neurodevelopmental outcomes of patients…
Continuous Renal Replacement Therapy in NICU — Indian Experience
M. S. Pillai
H. A. Venkatesh
The Indian Journal of Pediatrics
Corpus ID: 207388629
To the Editor : Continuous renal replacement therapy (CRRT) is an extracorporeal blood purification therapy intended to…
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.
Corpus ID: 84831
BACKGROUND Tandem mass spectrometry (MS/MS) is rapidly being adopted by newborn screening programs to screen dried blood spots…
Neonatal arginosuccinic aciduria.
Corpus ID: 27106933
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