Literature DB >> 14454131

Glucoglycinuria, a new familial syndrome.

H KASER, P COTTIER, I ANTENER.   

Abstract

Entities:  

Keywords:  GLYCOSURIA/genetics; PANCREATIC CYSTIC FIBROSIS/complications

Mesh：

Year:  1962        PMID： 14454131     DOI： 10.1016/s0022-3476(62)80369-2

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  5 in total

1.  HYPERGLYCINAEMIA AND HYPERGLYCINURIA IN A NEWBORN INFANT.

Authors:  H K VISSER; H W VEENSTRA; C PIK
Journal:  Arch Dis Child       Date:  1964-08       Impact factor: 3.791

Review 2.  INHERITED ENZYME DEFECTS: A REVIEW.

Authors:  T HARGREAVES
Journal:  J Clin Pathol       Date:  1963-07       Impact factor: 3.411

Review 3.  Lessons from inborn errors of metabolism.

Authors:  M D Milne
Journal:  Proc R Soc Med       Date:  1966-11

4.  Phenylketonuria with familial hyperglycinuria.

Authors:  J M Marques
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

5.  Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters.

Authors:  Stefan Bröer; Charles G Bailey; Sonja Kowalczuk; Cynthia Ng; Jessica M Vanslambrouck; Helen Rodgers; Christiane Auray-Blais; Juleen A Cavanaugh; Angelika Bröer; John E J Rasko
Journal:  J Clin Invest       Date:  2008-11-06       Impact factor: 14.808
  5 in total

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