Literature DB >> 14116920

HARTNUP DISEASE IN TWO SIBLINGS. CLINICAL OBSERVATIONS AND BIOCHEMICAL STUDIES.

J K VISAKORPI, L HJELT, T LAHIKAINEN, S OHMAN.   

Abstract

Keywords:  ADOLESCENCE; AMINOACIDURIA, RENAL; ATAXIA; CHILD; ECZEMA; GENETICS, HUMAN; NAD; NADP; NICOTINIC ACID; PELLAGRA; PROTEIN DEFICIENCY; TRYPTOPHAN

Mesh：

Substances：

Year:  1964        PMID： 14116920

Source DB:  PubMed          Journal:  Ann Paediatr Fenn        ISSN： 0570-1732


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  3 in total

1.  Hartnup syndrome, progressive encephalopathy and allo-albuminaemia. A clinico-pathological case study.

Authors:  K Schmidtke; W Endres; A Roscher; H Ibel; N Herschkowitz; C Bachmann; E Plöchl; H B Hadorn
Journal:  Eur J Pediatr       Date:  1992-12       Impact factor: 3.183

2.  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

3.  Hartnup disease.

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

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