Literature DB >> 1779640

A case of 6-pyruvoyl-tetrahydropterin synthase deficiency after screening 1,500,000 newborns in Greece.

K H Schulpis1, A Covanis, M Loumakou, N Frantzis, O Papandreou, A Divolli, S Missiou-Tsagaraki, L Kierat, N Blau.   

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Year:  1991        PMID： 1779640     DOI： 10.1007/bf01799967

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  3 in total

1.  Progression of 6-pyruvoyl-tetrahydropterin synthase deficiency from a peripheral into a central phenotype.

Authors:  A Ponzone; N Blau; O Guardamagna; G B Ferrero; I Dianzani; W Endres
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Phenylketonuria in Greece: 12 years' experience.

Authors:  S Missiou-Tsagaraki; K Soulpi; M Loumakou
Journal:  J Ment Defic Res       Date:  1988-08

Review 3.  Inborn errors of pterin metabolism.

Authors:  N Blau
Journal:  Annu Rev Nutr       Date:  1988       Impact factor: 11.848
  3 in total

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