Literature DB >> 20791345

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

J B Stephenson, M S McBean.   

Abstract

Entities:  

Year:  1967        PMID: 20791345      PMCID: PMC1842751          DOI: 10.1136/bmj.3.5565.579

Source DB:  PubMed          Journal:  Br Med J        ISSN: 0007-1447


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  14 in total

1.  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

2.  ADVANCES IN THE MANAGEMENT OF PATIENT WITH PHENYLKETONURIA.

Authors:  B UMBARGER; H K BERRY; B S SUTHERLAND
Journal:  JAMA       Date:  1965-09-06       Impact factor: 56.272

3.  The early symptoms of phenylketonuria.

Authors:  M W PARTINGTON
Journal:  Pediatrics       Date:  1961-03       Impact factor: 7.124

4.  Further experiences in the treatment of phenylketonuria.

Authors:  A MONCRIEFF; R H WILKINSON
Journal:  Br Med J       Date:  1961-03-18

5.  An enzymatic spectrophotometric method for the determination of phenylalanine in blood.

Authors:  B N LA DU; P J MICHAEL
Journal:  J Lab Clin Med       Date:  1960-03

6.  The phenylalanine requirement of the normal infant.

Authors:  S E SNYDERMAN; E L PRATT; M W CHEUNG; P NORTON; L E HOLT; A E HANSEN; T C PANOS
Journal:  J Nutr       Date:  1955-06-10       Impact factor: 4.798

7.  Paper chromatographic method for estimation of phenylalanine.

Authors:  H K BERRY
Journal:  Proc Soc Exp Biol Med       Date:  1957-05

8.  Dietary and Biochemical Control of Phenylketonuria.

Authors:  F S Brimblecombe; J D Blainey; M E Stoneman; B S Wood
Journal:  Br Med J       Date:  1961-09-23

9.  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

10.  Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria.

Authors:  A J Schneider; S D Garrard
Journal:  J Pediatr       Date:  1966-05       Impact factor: 4.406

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  5 in total

1.  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

2.  Phenylketonuria.

Authors:  B E Clayton
Journal:  J Med Genet       Date:  1971-03       Impact factor: 6.318

3.  Mass screening of the newborn for metabolic disease.

Authors:  L I Woolf
Journal:  Arch Dis Child       Date:  1968-04       Impact factor: 3.791

4.  Classical and mild phenylketonuria in a family.

Authors:  N A Coutts; W M Fyfe
Journal:  Arch Dis Child       Date:  1971-08       Impact factor: 3.791

5.  Biopterin defect in a normal-appearing child affected by a transient phenylketonuria.

Authors:  F Rey; R J Leeming; J A Blair; J Rey
Journal:  Arch Dis Child       Date:  1980-08       Impact factor: 3.791

  5 in total

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