Literature DB >> 5946447

Idiopathic hyperglycinemia: isolation and identification of three previously undescribed urinary ketones.

J H Menkes.   

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Year:  1966        PMID： 5946447     DOI： 10.1016/s0022-3476(66)80086-0

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


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  5 in total

1.  Inherited propionyl-Coa carboxylase deficiency in "ketotic hyperglycinemia".

Authors:  Y E Hsia; K J Scully; L E Rosenberg
Journal:  J Clin Invest       Date:  1971-01       Impact factor: 14.808

2.  Excretion of 2-methyl-3-oxovaleric acid in propionic acidemia.

Authors:  W Lehnert; L Schuchmann; R Urbánek; H Niederhoff; N Böhm
Journal:  Eur J Pediatr       Date:  1978-07-03       Impact factor: 3.183

Review 3.  [Methylmalonic aciduria. Classification, diagnosis and therapy (author's transl)].

Authors:  D Leupold
Journal:  Klin Wochenschr       Date:  1977-01-15

4.  Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels.

Authors:  H Przyrembel; H J Bremer; M Duran; L Bruinvis; D Ketting; S K Wadman; R Baumgartner; U Irle; C Bachmann
Journal:  Eur J Pediatr       Date:  1979-01-18       Impact factor: 3.183

5.  Tiglicaciduria in propionicacidaemia.

Authors:  W L Nyhan; T Ando; K Rasmussen; W Wadlington; A W Kilroy; D Cottom; D Hull
Journal:  Biochem J       Date:  1972-02       Impact factor: 3.857
  5 in total

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