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Arginosuccinic aciduria
Known as:
arginosuccinate lyase deficiency
National Institutes of Health
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Related topics
Related topics
4 relations
Broader (3)
Argininosuccinic Aciduria
Enzyme Deficiency
Urea 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
Jun Kido
,
Shirou Matsumoto
,
H. Mitsubuchi
,
F. Endo
,
Kimitoshi Nakamura
Metabolic Brain Disease
2018
Corpus ID: 47020054
Urea cycle disorders (UCDs) are inherited metabolic diseases that lead to hyperammonemia. Neurodevelopmental outcomes of patients…
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Review
2016
Review
2016
Continuous Renal Replacement Therapy in NICU — Indian Experience
M. S. Pillai
,
N. Nagesh
,
H. A. Venkatesh
,
A. Razak
,
V. Siddini
The Indian Journal of Pediatrics
2016
Corpus ID: 207388629
To the Editor : Continuous renal replacement therapy (CRRT) is an extracorporeal blood purification therapy intended to…
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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.
T. Zytkovicz
,
E. Fitzgerald
,
+7 authors
G. Grady
Clinical chemistry
2001
Corpus ID: 84831
BACKGROUND Tandem mass spectrometry (MS/MS) is rapidly being adopted by newborn screening programs to screen dried blood spots…
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1981
1981
Neonatal arginosuccinic aciduria.
R. Kuttan
,
L. Devarajan
,
M. Jadhav
,
A. Radhakrishnan
Indian pediatrics
1981
Corpus ID: 27106933
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