Tetrahydrobiopterin Deficiency and an International Database of Patients

Author:

Blau N.,Dhondt Jean-Louis

Publisher

Springer US

Reference16 articles.

1. N. Blau, Inborn errors of pterin metabolism. Ann Rev Nutr. 8:185 (1988).

2. J.L. Dhondt, Strategy for the screening of tetrahydrobiopterin deficiency among hyperphenylalaninemic patients: 15-years experience. J Inherit Metab Dis. 14:117 (1991).

3. N. Blau, H.C. Curtius, T. Kuster, A. Matasovic, G. Schoedon, J.L. Dhondt, P. Guibaud, T. Giudici and M. Blaskovics, Primapterinuria: a new variant of atypical phenylketonuria. J Inherit Metab Dis. 12/2:335 (1989).

4. J.L. Dhondt, Tetrahydrobiopterin deficiency. Lessons from the analysis of 90 patients collected in the international register. Arch Fr Pediatr. 12:655 (1987).

5. J.L. Dhondt, Tetrahydrobiopterin deficiencies. Lessons from the compilation of 200 patients. Developmental Brain Dysfunction. 6:139 (1993).

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