Literature DB >> 5645685

Mass screening of the newborn for metabolic disease.

L I Woolf.   

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Year:  1968        PMID: 5645685      PMCID: PMC2019823          DOI: 10.1136/adc.43.228.137

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


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  18 in total

1.  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

2.  A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.

Authors:  R GUTHRIE; A SUSI
Journal:  Pediatrics       Date:  1963-09       Impact factor: 7.124

3.  Use of micromethod for phenylalanine in management of phenylketonuric patients.

Authors:  H K BERRY
Journal:  Clin Chem       Date:  1962-04       Impact factor: 8.327

Review 4.  Phenylketonuria 1967.

Authors:  D Y Hsia
Journal:  Dev Med Child Neurol       Date:  1967-10       Impact factor: 5.449

5.  Phenylketonuria. Mass screening of newborns in Ireland.

Authors:  S F Cahalane
Journal:  Arch Dis Child       Date:  1968-04       Impact factor: 3.791

6.  Results of routine screening for phenylketonuria in early infancy, Northern Ireland (1960-67).

Authors:  N A Carson; I J Carré; D W Neill
Journal:  Arch Dis Child       Date:  1968-04       Impact factor: 3.791

7.  Procedures for monitoring the low-phenylalanine diet in treatment of phenylketonuria.

Authors:  H K Berry; B Umbarger; B S Sutherland
Journal:  J Pediatr       Date:  1965-10       Impact factor: 4.406

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

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

9.  A rapid method for the detection of plasma phenylalanine.

Authors:  J P Mellon; A G Stiven
Journal:  J Med Lab Technol       Date:  1966-07

10.  Diagnosis of phenylketonuria (phenylalanine hydroxylase deficiency, temporary and permanent).

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

Review 1.  Phenylketonuria: a review.

Authors:  J S Yu
Journal:  Postgrad Med J       Date:  1970-07       Impact factor: 2.401

2.  Implications for clinical implementation of results of metabolic screening for amino acidopathies in the newborn.

Authors:  M I Griffiths
Journal:  Arch Dis Child       Date:  1971-12       Impact factor: 3.791

3.  Routine neonatal screening for phenylketonuria in the United Kingdom 1964-78. Medical Research Council Steering Committee for the MRC/DHSS Phenylketonuria Register.

Authors: 
Journal:  Br Med J (Clin Res Ed)       Date:  1981-05-23

4.  Dr. Louis Isaac Woolf: At the Forefront of Newborn Screening and the Diet to Treat Phenylketonuria-Biography to Mark His 100th Birthday.

Authors:  José Ramón Alonso-Fernández
Journal:  Int J Neonatal Screen       Date:  2020-08-03
  4 in total

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