Literature DB >> 2516181

Progressive systemic scleroderma in an infant with partial phenylketonuria.

M Haktan1, A Aydin, H Bahat, B Tuysuz, H Yazici, S Altay.   

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Year:  1989        PMID： 2516181     DOI： 10.1007/bf01802048

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


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  3 in total

1.  Phenylketonuria and scleroderma.

Authors:  E H Brown; H K Berry; J Olson; J Levinson
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

2.  Pseudoscleroderma and phenylketonuria.

Authors:  G Y Guillet; N Dore; J P Hehunstre; J Maleville; J Battin
Journal:  Int J Dermatol       Date:  1983-09       Impact factor: 2.736

3.  Tryptophan metabolism in a patient with phenylketonuria and scleroderma: a proposed explanation of the indole defect in phenylketonuria.

Authors:  K N Drummond; A F Michael; R A Good
Journal:  Can Med Assoc J       Date:  1966-04-16       Impact factor: 8.262
  3 in total

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