Literature DB >> 590278

Termination of dietary treatment in phenylketonuria.

B Cabalska, N Duczyńska, J Borzymowska, K Zorska, A Koślacz-Folga, K Bozkowa.   

Abstract

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Year:  1977        PMID： 590278     DOI： 10.1007/bf00477051

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


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  14 in total

1.  PHENYLKETONURIA.

Authors:  R S PAINE
Journal:  Clin Proc Child Hosp Dist Columbia       Date:  1964-06

2.  TERMINATION OF DIETARY TREATMENT FOR PHENYLKETONURIA.

Authors:  P R VANDEMAN
Journal:  Am J Dis Child       Date:  1963-11

3.  Termination of dietary treatment of phenylketonuria.

Authors:  F A HORNER; C W STREAMER; L L ALEJANDRINO; L H REED; F IBBOTT
Journal:  N Engl J Med       Date:  1962-01-11       Impact factor: 91.245

4.  WHEN TO STOP THE DIET IN PHENYLKETONURIA.

Authors:  A MONCRIEFF
Journal:  Dev Med Child Neurol       Date:  1964-02       Impact factor: 5.449

5.  Phenylketonuria: mental development, behavior, and termination of low phenylalanine diet.

Authors:  I M Hackney; W B Hanley; W Davidson; L Lindsao
Journal:  J Pediatr       Date:  1968-05       Impact factor: 4.406

6.  Behavioral consequences of increased phenylalanine intake by phenylketonuric children: a pilot study describing a methodology.

Authors:  W K Frankenburg; A D Goldstein; C O Olson
Journal:  Am J Ment Defic       Date:  1973-03

7.  What is the best age to discontinue the low phenylalanine diet in phenylketonuria? A presentation of some contributory data.

Authors:  C F Johnson
Journal:  Clin Pediatr (Phila)       Date:  1972-03       Impact factor: 1.168

8.  Biochemical and EEG studies in phenylketonuric children during phenylalanine tolerance testc.

Authors:  B E Clayton; A A Moncrieff; G Pampiglione; J Shepherd
Journal:  Arch Dis Child       Date:  1966-06       Impact factor: 3.791

9.  Evaluation of the effects of terminating the diet in phenylketonuria.

Authors:  G Solomons; L Keleske; E Opitz
Journal:  J Pediatr       Date:  1966-10       Impact factor: 4.406

10.  Results of treatment and termination of the diet in phenylketonuria (PKU).

Authors:  E S Kang; N D Sollee; P S Gerald
Journal:  Pediatrics       Date:  1970-12       Impact factor: 7.124
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  21 in total

1.  Effect on intelligence of relaxing the low phenylalanine diet in phenylketonuria.

Authors:  I Smith; M G Beasley; A E Ades
Journal:  Arch Dis Child       Date:  1991-03       Impact factor: 3.791

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.  The effects of diet discontinuation in children with phenylketonuria.

Authors:  R Koch; C G Azen; N Hurst; E G Friedman; K Fishler
Journal:  Eur J Pediatr       Date:  1987       Impact factor: 3.183

4.  Intracellular concentrations of phenylalanine, tyrosine and alpha-aminobutyric acid in 13 homozygotes and 19 heterozygotes for phenylketonuria compared with 26 normals.

Authors:  O Thalhammer; A Pollak; G Lubec; H Königshofer
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

5.  Late onset phenylalanine intoxication.

Authors:  L I Woolf
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

6.  Longitudinal study on early diagnosis and treatment of phenylketonuria in Poland.

Authors:  M B Cabalska; I Nowaczewska; E Sendecka; K Zorska
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

Review 7.  A prefrontal dysfunction model of early-treated phenylketonuria.

Authors:  M C Welsh
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

8.  Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria.

Authors:  I Smith; M E Lobascher; J E Stevenson; O H Wolff; H Schmidt; S Grubel-Kaiser; H Bickel
Journal:  Br Med J       Date:  1978-09-09

9.  Turnover of the fast components of myelin and myelin proteins in experimental hyperphenylalaninaemia. Relevance to termination of dietary treatment in human phenylketonuria.

Authors:  F A Hommes; A G Eller; E H Taylor
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

Review 10.  Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Medical Research Council Working Party on Phenylketonuria.

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