Literature DB >> 5927700

Hartnup disease in three siblings.

E G Nielsen, S Vedso, C Zimmermann-Nielsen.   

Abstract

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Year:  1966        PMID： 5927700

Source DB:  PubMed          Journal:  Dan Med Bull        ISSN： 0907-8916


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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.  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

4.  Xanthurenic aciduria due to a mutation in KYNU encoding kynureninase.

Authors:  M Christensen; M Duno; A M Lund; F Skovby; E Christensen
Journal:  J Inherit Metab Dis       Date:  2007-03-01       Impact factor: 4.750

5.  Tissue-specific amino acid transporter partners ACE2 and collectrin differentially interact with hartnup mutations.

Authors:  Simone M R Camargo; Dustin Singer; Victoria Makrides; Katja Huggel; Klaas M Pos; Carsten A Wagner; Keiji Kuba; Ursula Danilczyk; Flemming Skovby; Robert Kleta; Josef M Penninger; François Verrey
Journal:  Gastroenterology       Date:  2008-10-29       Impact factor: 22.682
  5 in total

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