Literature DB >> 13462804

Phenylketonuria.

W R CENTERWALL.   

Abstract

Entities:  

Keywords:  PHENYLPYRUVIC OLIGOPHRENIA/diagnosis

Mesh：

Year:  1957        PMID： 13462804     DOI： 10.1001/jama.1957.02980220076022

Source DB:  PubMed          Journal:  J Am Med Assoc        ISSN： 0002-9955


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  6 in total

1.  The detection and diagnosis of phenylketonuria.

Authors:  R J ALLEN
Journal:  Am J Public Health Nations Health       Date:  1960-11

2.  Phenylketonuria: screening programs and testing methods.

Authors:  W R CENTERWALL; R F CHINNOCK; A PUSAVAT
Journal:  Am J Public Health Nations Health       Date:  1960-11

3.  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

Review 4.  Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

Authors:  Suzanne W Boyer; Lisa J Barclay; Lindsay C Burrage
Journal:  Nutr Clin Pract       Date:  2015-06-16       Impact factor: 3.080

Review 5.  Newborn Screening for Primary Immunodeficiency Diseases: History, Current and Future Practice.

Authors:  Jovanka R King; Lennart Hammarström
Journal:  J Clin Immunol       Date:  2017-11-08       Impact factor: 8.317

6.  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
  6 in total

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