المؤلفون: Nagamani SC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA. nagamani@bcm.edu, Shchelochkov OA, Mullins MA, Carter S, Lanpher BC, Sun Q, Kleppe S, Erez A, O'Brian Smith E, Marini JC, Lee B

مؤلفون مشاركون: Members of the Urea Cycle Disorders Consortium

المصدر: Molecular genetics and metabolism [Mol Genet Metab] 2012 Nov; Vol. 107 (3), pp. 315-21. Date of Electronic Publication: 2012 Sep 17.

نوع المنشور: Journal Article; Randomized Controlled Trial; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE

مواضيع طبية MeSH: Arginine/*therapeutic use , Argininosuccinic Aciduria/*drug therapy , Phenylbutyrates/*therapeutic use, Adolescent ; Alanine Transaminase/blood ; Arginine/blood ; Argininosuccinic Acid/blood ; Argininosuccinic Aciduria/blood ; Aspartate Aminotransferases/blood ; Child ; Child, Preschool ; Cross-Over Studies ; Double-Blind Method ; Drug Administration Schedule ; Drug Therapy, Combination ; Female ; Humans ; Liver Function Tests ; Male ; Phenylbutyrates/blood ; Placebos ; Young Adult