Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrate

Ammonia control in children with urea cycle disorders (UCDs); Phase 2 comparison of sodium phenylbutyrate and glycerol phenylbutyrate

(2011) Uta Lichter-Konecki et al.   MOLECULAR GENETICS AND METABOLISM

Pharmacology and safety of glycerol phenylbutyrate in healthy adults and adults with cirrhosis

(2010) Brendan M. McGuire et al.   HEPATOLOGY

Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium

(2010) Jennifer Seminara et al.   MOLECULAR GENETICS AND METABOLISM

Phase 2 comparison of a novel ammonia scavenging agent with sodium phenylbutyrate in patients with urea cycle disorders: Safety, pharmacokinetics and ammonia control

(2010) Brendan Lee et al.   MOLECULAR GENETICS AND METABOLISM

Experimental models of hepatic encephalopathy: ISHEN guidelines

(2009) Roger F. Butterworth et al.   LIVER INTERNATIONAL

Clinical trials: Curing a critical deficiency in metabolic medicine

(2009) Jerry Vockley et al.   MOLECULAR GENETICS AND METABOLISM

Treatment of mitochondrial electron transport chain disorders: A review of clinical trials over the past decade

(2009) Douglas S. Kerr   MOLECULAR GENETICS AND METABOLISM

Intellectual, Adaptive, and Behavioral Functioning in Children With Urea Cycle Disorders

(2009) Lauren Krivitzky et al.   PEDIATRIC RESEARCH

1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency

(2008) A.L. Gropman et al.   MOLECULAR GENETICS AND METABOLISM

Cross-sectional multicenter study of patients with urea cycle disorders in the United States

(2008) Mendel Tuchman et al.   MOLECULAR GENETICS AND METABOLISM