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The New England journal of medicine, ISSN 1533-4406, 02/2014, Volume 370, Issue 6, pp. 533 - 542
Journal Article
Genetics in medicine, ISSN 1098-3600, 05/2012, Volume 14, Issue 5, pp. 501 - 507
.... Deficiencies of any of these enzymes of the cycle result in urea cycle disorders (UCDs), a group of inborn errors of hepatic metabolism that often result in life-threatening hyperammonemia... 
argininosuccinic aciduria | nitric oxide | arginine | urea cycle | argininosuccinate lyase | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Liver Transplantation | Phenylbutyrates - therapeutic use | Genetic Testing | Humans | Child, Preschool | Infant | Neonatal Screening | Argininosuccinic Aciduria - diagnosis | Argininosuccinic Acid - urine | Hyperammonemia - enzymology | Liver Diseases - enzymology | Argininosuccinic Acid - metabolism | Hypertension - enzymology | Hypertension - genetics | Citrulline - blood | Infant, Newborn | Cognition Disorders - enzymology | Hyperammonemia - genetics | Liver Diseases - genetics | Argininosuccinate Lyase - genetics | Argininosuccinic Aciduria - therapy | Cognition Disorders - genetics | Lipids - therapeutic use | Diet, Protein-Restricted | Argininosuccinic Acid - blood | Argininosuccinic Aciduria - genetics | Fumarates - metabolism | Sodium Benzoate - therapeutic use | Glucose - therapeutic use | Arginine - therapeutic use | Arginine - metabolism | Index Medicus | Urine | Enzymes | Intravenous administration | Liver diseases | Liver | Cognition | Transplantation | Glucose | Metabolism | Nitrogen | Genetic screening | Argininosuccinate lyase | Dietary restrictions | Urea | Arginine | hyperammonemia | Wastes | citrulline | Genotypes | Argininosuccinic aciduria | Argininosuccinate Lyase
Journal Article
Journal Article