Literature DB >> 14320688

THE HURLER SYNDROME: A BIOCHEMICAL AND CLINICAL STUDY.

A G BEARN.   

Abstract

Keywords:  ADOLESCENCE; BIOCHEMISTRY; CHILD; CHONDROITIN; ELECTROPHORESIS; EXCRETION; GENETICS, HUMAN; LIPOCHONDRODYSTROPHY; MUCOPOLYSACCHARIDES; URINE

Mesh：

Substances：

Year:  1965        PMID： 14320688     DOI： 10.1016/0002-9343(65)90045-8

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


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  3 in total

1.  The genetic secrets of the humble fibroblast.

Authors:  A G Bearn; B S Danes
Journal:  Trans Am Clin Climatol Assoc       Date:  1970

2.  Biochemical definition of the mucopolysaccharidoses.

Authors:  J W Spranger
Journal:  Z Kinderheilkd       Date:  1970

3.  [The heparitinsulfate mucopolysaccharidosis (Sanfilippo). Clinical, biochemical, genetic and morphological studies].

Authors:  W Teller; H Bechtelsheimer; V Totović
Journal:  Klin Wochenschr       Date:  1967-05-15
  3 in total

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