Literature DB >> 8929743

Microcephaly in a hyperphenylalaninemic infant leading to the diagnosis of maternal hyperphenylalaninemia.

N Gungor, A Tokath, T Coskun, M Ozguc, I Ozalp.   

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Year:  1996        PMID： 8929743     DOI： 10.1007/bf01953954

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


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  5 in total

1.  Inherited metabolic disorders in Turkey.

Authors:  I Ozalp; T Coskun; S Tokol; G Demircin; E Mönch
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Effects of untreated maternal hyperphenylalaninemia on the fetus: further study of families identified by routine cord blood screening.

Authors:  S E Waisbren; H L Levy
Journal:  J Pediatr       Date:  1990-06       Impact factor: 4.406

3.  Phenylalanine embryopathy in three siblings: implications of maternal diet therapy.

Authors:  R P Bachman; E J Schoen; M V Backstrom; R L Lee; S R Williams; E R Jurecki
Journal:  Am J Dis Child       Date:  1993-01

4.  Maternal phenylketonuria.

Authors:  D H Pullon; S D Macfarlane; I C Lyon
Journal:  N Z Med J       Date:  1990-08-22

5.  Effects of untreated maternal phenylketonuria and hyperphenylalaninemia on the fetus.

Authors:  H L Levy; S E Waisbren
Journal:  N Engl J Med       Date:  1983-11-24       Impact factor: 91.245
  5 in total
  1 in total

1.  Microcephaly and maternal phenylketonuria.

Authors:  A Superti-Furga; B Steinmann; G Duc; R Gitzelmann
Journal:  Eur J Pediatr       Date:  1996-11       Impact factor: 3.183
  1 in total

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