Efficacy and safety of i.v. sodium benzoate in urea cycle disorders: a multicentre retrospective study

[1]  S. Waisbren,et al.  Improving long term outcomes in urea cycle disorders-report from the Urea Cycle Disorders Consortium , 2016, Journal of Inherited Metabolic Disease.

[2]  J. Zeman,et al.  Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders , 2016, Journal of Inherited Metabolic Disease.

[3]  S. Kölker,et al.  Neonatal mortality and outcome at the end of the first year of life in early onset urea cycle disorders—review and meta-analysis of observational studies published over more than 35 years , 2016, Journal of Inherited Metabolic Disease.

[4]  M. Baumgartner,et al.  The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation , 2015, Journal of Inherited Metabolic Disease.

[5]  M. Tuchman,et al.  A longitudinal study of urea cycle disorders. , 2014, Molecular genetics and metabolism.

[6]  Hye-Seung Lee,et al.  The incidence of urea cycle disorders. , 2013, Molecular genetics and metabolism.

[7]  M. Baumgartner,et al.  Cross-sectional observational study of 208 patients with non-classical urea cycle disorders , 2013, Journal of Inherited Metabolic Disease.

[8]  V. Rubio,et al.  Suggested guidelines for the diagnosis and management of urea cycle disorders , 2012, Orphanet Journal of Rare Diseases.

[9]  Sanjay Saint,et al.  Guidelines for the prevention of intravascular catheter-related infections. , 2002, American journal of infection control.

[10]  Sanjay Saint,et al.  Guidelines for the prevention of intravascular catheter-related infections. , 2011, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

[11]  V. Walker,et al.  Ammonia toxicity and its prevention in inherited defects of the urea cycle , 2009, Diabetes, obesity & metabolism.

[12]  F. Feillet,et al.  Conduite à tenir devant une hyperammoniémie , 2009 .

[13]  F. Feillet,et al.  [Diagnosis and management of hyperammonemia]. , 2009, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

[14]  J. Leonard,et al.  Hypothesis: proposals for the management of a neonate at risk of hyperammonaemia due to a urea cycle disorder , 2008, European Journal of Pediatrics.

[15]  A. Hamosh,et al.  Survival after treatment with phenylacetate and benzoate for urea-cycle disorders. , 2007, The New England journal of medicine.

[16]  M. Meisner,et al.  [Patients with ornithine transcarbamylase deficiency. Anaesthesiological and intensive care management]. , 2005, Der Anaesthesist.

[17]  S. Albrecht,et al.  Der Patient mit Ornithintranscarbamylasemangel , 2005, Der Anaesthesist.

[18]  D. Kovacevich,et al.  Guidelines for the prevention of intravascular catheter-related infections: Centers for Disease Control and Prevention. , 2003, Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition.

[19]  M. Tuchman,et al.  Proceedings of a consensus conference for the management of patients with urea cycle disorders. , 2001, The Journal of pediatrics.

[20]  M. Braun,et al.  Continuous Venovenous Hemodiafiltration in the Treatment of Acute Hyperammonemia , 1998, American Journal of Nephrology.

[21]  J. Leonard,et al.  Alternative pathway therapy for urea cycle disorders , 1998, Journal of Inherited Metabolic Disease.

[22]  P. D. Lonlay,et al.  Les maladies héréditaires du métabolisme à l'âge adulte , 1998 .

[23]  J. Saudubray,et al.  [Hereditary metabolic diseases in adults]. , 1998, La Revue de medecine interne.

[24]  S. Brusilow,et al.  Urea cycle disorders: diagnosis, pathophysiology, and therapy. , 1996, Advances in Pediatrics.

[25]  M. Msall,et al.  Cognitive Development in Children with Inborn Errors of Urea Synthesis , 1988, Acta paediatrica Japonica : Overseas edition.

[26]  D. Rabier,et al.  VALPROATE-INDUCED INHIBITION OF UREA SYNTHESIS , 1987, The Lancet.

[27]  S. Brusilow,et al.  Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies. , 1984, The New England journal of medicine.

[28]  N. Buchan.  Letter: Breast examination in obese patients. , 1976, Lancet.