Pages that link to "Q36062700"
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The following pages link to Carbamylphosphate synthetase deficiency in an infant with severe cerebral damage (Q36062700):
Displaying 16 items.
- Disorders of amino acid metabolism--1971 (Q34825350) (← links)
- Neonatal hyperammonaemia with complete absence of liver carbamyl phosphate synthetase activity (Q34986724) (← links)
- Neuropathological observations in a patient with carbamylphosphate-synthetase deficiency and in two sibs (Q35149402) (← links)
- Autosomal recessive inheritance of human mitochondrial carbamyl phosphate synthetase deficiency. (Q35201486) (← links)
- Genetic-Metabolic Considerations in the Sick Neonate (Q39772163) (← links)
- Phenylketonuria and Other Disorders of Amino Acid Metabolism (Q39926030) (← links)
- Treatment of Carbamyl Phosphate Synthetase Deficiency with Keto Analogues of Essential Amino Acids (Q39929473) (← links)
- Regulation of pyrimidine and arginine biosynthesis in mammals (Q40003082) (← links)
- Carbamyl-phosphate-synthetase deficiency with neonatal onset of symptoms (Q40095808) (← links)
- Carbamyl phosphate synthetase 1 deficiency: a destructive encephalopathy (Q43574492) (← links)
- Liver Morphology in a Case of Citrullinemia (a Light and Electron Microscopic Study) (Q44277466) (← links)
- Congenital hyperammonemic syndromes (Q44778177) (← links)
- Liver pathology in a new congenital disorder of urea synthesis: N-acetylglutamate synthetase deficiency (Q69976931) (← links)
- Kinetic abnormalities of carbamyl phosphate synthetase-I in a case of congenital hyperammonaemia (Q70316913) (← links)
- Carbamyl phosphate synthetase deficiency with lethal neonatal outcome (Q70599251) (← links)
- Ultrastructure of hepatic mitochondria in a child with hyperornithinemia, hyperammonemia, and homocitrullinuria (Q70762041) (← links)