Literature DB >> 5673397

Paediatric screening for genetically determined metabolic diseases.

L I Woolf.   

Abstract

Mesh：

Substances：

Year:  1968        PMID： 5673397      PMCID： PMC1902463     

Source DB:  PubMed          Journal:  Proc R Soc Med        ISSN： 0035-9157


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  6 in total

1.  APPLICATION OF A SIMPLE MICROMETHOD TO THE SCREENING OF PLASMA FOR A VARIETY OF AMINOACIDOPATHIES.

Authors:  C R SCRIVER; E DAVIES; A M CULLEN
Journal:  Lancet       Date:  1964-08-01       Impact factor: 79.321

2.  A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER.

Authors:  M L EFRON; D YOUNG; H W MOSER; R A MACCREADY
Journal:  N Engl J Med       Date:  1964-06-25       Impact factor: 91.245

3.  AN AUTOMATED PROCEDURE FOR BLOOD PHENYLALANINE.

Authors:  J B HILL; G K SUMMER; M W PENDER; N O ROSZEL
Journal:  Clin Chem       Date:  1965-05       Impact factor: 8.327

4.  Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives.

Authors:  N K GIBBS; L I WOOLF
Journal:  Br Med J       Date:  1959-09-26

5.  Phenylketonuria: a reassessment of mass infant screening by napkin test.

Authors:  J B Stephenson; M S McBean
Journal:  Br Med J       Date:  1967-09-02

6.  A manual fluorometric paper disc method for detecting phenylketonuria.

Authors:  B Searle; M B Mijuskovic; D Widelock; B Davidow
Journal:  Clin Chem       Date:  1967-08       Impact factor: 8.327
  6 in total

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