Literature DB >> 5647741

Hartnup disorder in a New England family.

J Pomeroy, M L Efron, J Dayman, D Hoefnagel.   

Abstract

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Year:  1968        PMID： 5647741     DOI： 10.1056/NEJM196805302782207

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  5 in total

1.  Hartnup disease.

Authors:  M D Milne
Journal:  Biochem J       Date:  1969-02       Impact factor: 3.857

2.  Studies on intestinal absorption of amino acids and a dipeptide in a case of Hartnup disease.

Authors:  F Navab; A M Asatoor
Journal:  Gut       Date:  1970-05       Impact factor: 23.059

3.  The Hartnup phenotype: Mendelian transport disorder, multifactorial disease.

Authors:  C R Scriver; B Mahon; H L Levy; C L Clow; T M Reade; J Kronick; B Lemieux; C Laberge
Journal:  Am J Hum Genet       Date:  1987-05       Impact factor: 11.025

4.  Circumvention of defective neutral amino acid transport in Hartnup disease using tryptophan ethyl ester.

Authors:  A J Jonas; I J Butler
Journal:  J Clin Invest       Date:  1989-07       Impact factor: 14.808

5.  A candidate mouse model for Hartnup disorder deficient in neutral amino acid transport.

Authors:  D J Symula; A Shedlovsky; E N Guillery; W F Dove
Journal:  Mamm Genome       Date:  1997-02       Impact factor: 2.957
  5 in total

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