arginine and Carbamoyl-Phosphate Synthase I Deficiency Disease

arginine has been researched along with Carbamoyl-Phosphate Synthase I Deficiency Disease in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (25.00)29.6817
2010's2 (50.00)24.3611
2020's1 (25.00)2.80

Authors

AuthorsStudies
Ando, Y; Arisaka, O; Imataka, G; Ishii, J; Nitta, A; Takagi, Y; Yoshihara, S1
Cynober, L; Forbes, A; Osowska, S; Papadia, C1
Mhanni, AA; Prasad, C; Rockman-Greenberg, C1
Brunetti-Pierri, N; Carter, S; Garlick, P; Jahoor, F; Kleppe, S; Lee, B; Marini, J; O'Brien, W; Scaglia, F1

Reviews

2 review(s) available for arginine and Carbamoyl-Phosphate Synthase I Deficiency Disease

ArticleYear
Citrulline in health and disease. Review on human studies.
    Clinical nutrition (Edinburgh, Scotland), 2018, Volume: 37, Issue:6 Pt A

    Topics: Anabolic Agents; Animals; Arginine; Athletic Performance; Carbamoyl-Phosphate Synthase I Deficiency Disease; Cardiovascular Diseases; Citrulline; Endothelial Cells; Enterocytes; Female; Humans; Immunity; Male; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Oxidative Stress; Protein Biosynthesis; Urea Cycle Disorders, Inborn

2018
Clinical consequences of urea cycle enzyme deficiencies and potential links to arginine and nitric oxide metabolism.
    The Journal of nutrition, 2004, Volume: 134, Issue:10 Suppl

    Topics: Animals; Arginine; Argininosuccinic Aciduria; Carbamoyl-Phosphate Synthase I Deficiency Disease; Enzymes; Humans; Hyperargininemia; Isoenzymes; Metabolism, Inborn Errors; Nitric Oxide; Urea

2004

Other Studies

2 other study(ies) available for arginine and Carbamoyl-Phosphate Synthase I Deficiency Disease

ArticleYear
Long-term survival of a patient with acute neonatal-onset metabolic encephalopathy with carbamoyl phosphate synthetase 1 deficiency.
    European review for medical and pharmacological sciences, 2020, Volume: 24, Issue:19

    Topics: Arginine; Brain Diseases, Metabolic; Carbamoyl-Phosphate Synthase I Deficiency Disease; Carnitine; Female; Humans; Hyperammonemia; Infant, Newborn; Phenylbutyrates; Renal Dialysis; Sodium Benzoate

2020
Ornithine transcarbamylase deficiency presenting as recurrent abdominal pain in childhood.
    Pediatric emergency care, 2011, Volume: 27, Issue:9

    Topics: Abdominal Pain; Alkalosis, Respiratory; Arginine; Carbamoyl-Phosphate Synthase I Deficiency Disease; Child, Preschool; Citrulline; Consciousness Disorders; Diagnosis, Differential; Diet, Protein-Restricted; Emergencies; Exons; Female; Glutamine; Humans; Hyperammonemia; Language Development Disorders; Liver Transplantation; Mutation, Missense; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Phenylbutyrates; Recurrence

2011