M. Lambert

Guanidino Compound Analysis as a Complementary Diagnostic Parameter for Hyperargininemia: Follow-Up of Guanidino Compound Levels during Therapy

P. Deyn, S. Cederbaum, A. Lowenthal, 1990, Pediatric Research.

Hyperargininemia: intellectual and motor improvement related to changes in biochemical data.

P. D. De Deyn, L. Dallaire, B. Marescau, 1991, The Journal of pediatrics.

Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: neurologic, ophthalmologic, and neuropsychologic examination of six patients.

G. Mitchell, J. Lemay, J. Dubé, 1992, The Journal of pediatrics.

Hyperornithinemia, hyperammonemia, homocitrullinuria (HHH) syndrome: presentation as acute liver disease with coagulopathy.

E. Seidman, G. Jasmin, P. Brochu, 1992, Journal of Pediatric Gastroenterology and Nutrition - JPGN.

Guanidino compounds in hyperargininaemia

E. Hirsch, M. Durán, S. Cederbaum, 1992 .

Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal.

D. Millington, L. Dallaire, S. Melançon, 1996, Biochemical and molecular medicine.

Hyperargininemia: a treatable inborn error of metabolism?

R. C. Green, A. Beaudet, E. Hirsch, 1997 .

Hyperorgininemia: a treatable inborn error of metabolism

Roth, A. Beaudet, S. Cederbaum, 1997 .

Nucleotide pool imbalances in the livers of patients with urea cycle disorders associated with increased levels of orotic aciduria.

S. Rajalakshmi, D. Sarma, S. Vasudevan, 1995, Biochemistry and molecular biology international.