Literature DB >> 4935772

Phenylketonuria and its variations. A review of recent developments.

M E Blaskovics, T L Nelson.   

Abstract

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Year:  1971        PMID： 4935772      PMCID： PMC1517901     

Source DB:  PubMed          Journal:  Calif Med        ISSN： 0008-1264


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  108 in total

1.  UNEXPECTED FINDING FROM A PKU NEWBORN SCREENING PROGRAM.

Authors:  R W COFFELT
Journal:  Pediatrics       Date:  1964-12       Impact factor: 7.124

2.  The dietary treatment of phenylketonuria.

Authors:  L I WOOLF; R GRIFFITHS; A MONCRIEFF; S COATES; F DILLISTONE
Journal:  Arch Dis Child       Date:  1958-02       Impact factor: 3.791

3.  Phenylketonuria. Report of the Oregon Detection and Evaluation Program.

Authors:  J M Stewart; C G Ashley
Journal:  J Lancet       Date:  1967-05

4.  Cystathioninuria in two healty siblings.

Authors:  T L Perry; D F Hardwick; S Hansen; D L Love; S Israels
Journal:  N Engl J Med       Date:  1968-03-14       Impact factor: 91.245

5.  Termination of dietary treatment of phenylketonuria.

Authors:  D Murphy
Journal:  Ir J Med Sci       Date:  1969-04       Impact factor: 1.568

6.  Congenital malformations in offspring of phenylketonuric mothers.

Authors:  R E Stevenson; C C Huntley
Journal:  Pediatrics       Date:  1967-07       Impact factor: 7.124

7.  The effect of excess L-phenylalamine on mothers and on their breast-fed infants.

Authors:  R O Fisch; R Jenness; D Doeden; J A Anderson
Journal:  J Pediatr       Date:  1967-08       Impact factor: 4.406

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.  Legislation and advances in medical knowledge--acceleration or inhibition?

Authors:  S P Bessman
Journal:  J Pediatr       Date:  1966-08       Impact factor: 4.406

10.  PREVENTION OF A MENTAL DEFECT OF PHENYLKETONURIA WITH SEROTONIN CONGENERS SUCH AS MELATONIN OR HYDROXYTRYPTOPHAN.

Authors:  D W WOOLLEY; T VANDERHOEVEN
Journal:  Science       Date:  1964-06-26       Impact factor: 47.728
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  16 in total

1.  Increased neurotransmitter biosynthesis in phenylketonuria induced by phenylalanine restriction or by supplementation of unrestricted diet with large amounts of tyrosine.

Authors:  C Lykkelund; J B Nielsen; H C Lou; V Rasmussen; A M Gerdes; E Christensen; F Güttler
Journal:  Eur J Pediatr       Date:  1988-12       Impact factor: 3.183

2.  Hypophosphatasia with phenylketonuria.

Authors:  M E Blaskovics; K N Shaw
Journal:  Z Kinderheilkd       Date:  1974

3.  Phenylalaninaemia. Differential diagnosis.

Authors:  M E Blaskovics; G E Schaeffler; S Hack
Journal:  Arch Dis Child       Date:  1974-11       Impact factor: 3.791

Review 4.  Diet termination in children with phenylketonuria: a review of psychological assessments used to determine outcome.

Authors:  S E Waisbren; R R Schnell; H L Levy
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

5.  Effects of increasing Mg++ ion concentration on the PKU monitoring assay.

Authors:  K J Brown; R B Elliott; D R Lines
Journal:  Experientia       Date:  1979-04-15

Review 6.  Inborn errors of metabolism: clues to understanding human behavioral disorders.

Authors:  G S Omenn
Journal:  Behav Genet       Date:  1976-07       Impact factor: 2.805

7.  Compound heterozygotes in hyperphenylalaninaemia.

Authors:  K Bartholomé; K Olek; F Trefz
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

8.  [Molecular basis for the heterogeneity of phenylketonuria].

Authors:  K Bartholomé
Journal:  Naturwissenschaften       Date:  1980-10

Review 9.  Diseases of phenylalanine metabolism.

Authors:  C E Parker
Journal:  West J Med       Date:  1979-10

10.  Phenylketonuria (PKU) and the single gene: an old story retold.

Authors:  R M Murphey
Journal:  Behav Genet       Date:  1983-03       Impact factor: 2.805
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