Literature DB >> 14085009

CLINICAL AND BIOCHEMICAL FEATURES OF A CASE OF HARTNUP DISEASE.

S G SRIKANTIA, P S VENKATACHALAM, V REDDY.   

Abstract

Keywords:  AMINOACIDURIA, RENAL; BIOCHEMISTRY; CHILD; GENETICS, HUMAN; INDICAN; INDOLEACETIC ACID; KIDNEY DISEASES; PELLAGRA; TRYPTOPHAN; URINE

Mesh：

Substances：

Year:  1964        PMID： 14085009      PMCID： PMC1813320          DOI： 10.1136/bmj.1.5378.282

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


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  3 in total

1.  The metabolic disorder in Hartnup disease.

Authors:  M D MILNE; M A CRAWFORD; C B GIRAO; L W LOUGHRIDGE
Journal:  Q J Med       Date:  1960-07

2.  Formation of indole-3-acetic acid and tryptamine in animals: a method for estimation of indole-3-acetic acid in tissues.

Authors:  H WEISSBACH; W KING; A SJOERDSMA; S UDENFRIEND
Journal:  J Biol Chem       Date:  1959-01       Impact factor: 5.157

3.  Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features.

Authors:  D N BARON; C E DENT; H HARRIS; E W HART; J B JEPSON
Journal:  Lancet       Date:  1956-09-01       Impact factor: 79.321
  3 in total
  4 in total

1.  Clinical and biochemical observations in two cases of hartnup disease.

Authors:  P W Wong; P M Pillai
Journal:  Arch Dis Child       Date:  1966-08       Impact factor: 3.791

2.  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

3.  Biochemical screening and mental retardation.

Authors:  B S Sridhara Rama Rao; N Jayasimha; M N Subhash
Journal:  Indian J Pediatr       Date:  1982 May-Jun       Impact factor: 1.967

Review 4.  The role of the neutral amino acid transporter B0AT1 (SLC6A19) in Hartnup disorder and protein nutrition.

Authors:  Stefan Bröer
Journal:  IUBMB Life       Date:  2009-06       Impact factor: 3.885
  4 in total

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