Glutamine and hyperammonemic crises in patients with urea cycle disorders
B. Lee(Baylor College of Medicine), Bruce F. Scharschmidt, Cary O. Harding(Oregon Health & Science University), Andreas Schulze(University of Toronto), George A. Díaz(Icahn School of Medicine at Mount Sinai), Dion F. Coakley, William Berquist(Palo Alto University), Richard Rowell, Wendy E. Smith(Maine Medical Center), Cynthia Le Mons(National Urea Cycle Disorders Foundation), Masoud Mokhtarani, Uta Lichter‐Konecki(Children's National), Miguel Marino(Tufts Medical Center), Nicola Longo(Center for Human Genetics), Annette Feigenbaum(Hospital for Sick Children), Shawn E. McCandless(University Hospitals of Cleveland), James Bartley(MemorialCare Long Beach Medical Center), S.C. Nagamani(Baylor College of Medicine), Susan A. Berry(University of Minnesota), Renata C. Gallagher(Children's Hospital Colorado), William J. Rhead(Children's Hospital of Wisconsin)
Cited by 41
Related Papers
Cockayne syndrome: Review of 140 cases
|American Journal of Medical Genetics|1992|807
B cell–helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen
|Nature Immunology|2011|724
Phenylalanine hydroxylase deficiency: diagnosis and management guideline
|Genetics in Medicine|2014|718
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
|Genetics in Medicine|2017|563
Treatment of Fabry’s Disease with the Pharmacologic Chaperone Migalastat
|New England Journal of Medicine|2016|555