Literature DB >> 6502349

Intelligence and personality characteristics in adults with untreated atypical phenylketonuria and mild hyperphenylalaninemia.

S E Waisbren, R Schnell, H L Levy.   

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Year:  1984        PMID： 6502349     DOI： 10.1016/s0022-3476(84)80088-8

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  11 in total

Review 1.  Phenylketonuria: old disease, new approach to treatment.

Authors:  H L Levy
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

2.  Randomised controlled trial of tyrosine supplementation on neuropsychological performance in phenylketonuria.

Authors:  M L Smith; W B Hanley; J T Clarke; P Klim; W Schoonheyt; V Austin; D C Lehotay
Journal:  Arch Dis Child       Date:  1998-02       Impact factor: 3.791

3.  DNA haplotype analyses of patients with hyperphenylalaninemia.

Authors:  D Di Silvestre; A Pandya; R Koch; J Groffen
Journal:  Am J Hum Genet       Date:  1990-10       Impact factor: 11.025

4.  Commentary: What degree of hyperphenylalaninaemia requires treatment?

Authors:  R J Pollitt
Journal:  J Inherit Metab Dis       Date:  2012-06-21       Impact factor: 4.982

5.  Behavioural and emotional problems in early-treated adolescents with phenylketonuria in comparison with diabetic patients and healthy controls.

Authors:  J Weglage; M Grenzebach; M Pietsch; R Feldmann; R Linnenbank; J Denecke; H G Koch
Journal:  J Inherit Metab Dis       Date:  2000-07       Impact factor: 4.982

6.  Expression of human phenylalanine hydroxylase activity in T lymphocytes of classical phenylketonuria children by retroviral-mediated gene transfer.

Authors:  C M Lin; Y Tan; Y M Lee; C C Chang; K J Hsiao
Journal:  J Inherit Metab Dis       Date:  1997-11       Impact factor: 4.982

7.  Intelligence in mild atypical phenylketonuria.

Authors:  P M Costello; M G Beasley; S L Tillotson; I Smith
Journal:  Eur J Pediatr       Date:  1994-04       Impact factor: 3.183

8.  The North American Maternal Phenylketonuria Collaborative Study, developmental assessment of the offspring: preliminary report.

Authors:  W B Hanley; R Koch; H L Levy; R Matalon; B Rouse; C Azen; F de la Cruz
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

Review 9.  Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Medical Research Council Working Party on Phenylketonuria.

Authors: 
Journal:  BMJ       Date:  1993-01-09

10.  The New England Maternal PKU Project: identification of at-risk women.

Authors:  S E Waisbren; L B Doherty; I V Bailey; F J Rohr; H L Levy
Journal:  Am J Public Health       Date:  1988-07       Impact factor: 9.308
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