Literature DB >> 31423

Methylmalonyl-CoA mutase deficiency associated with severe neonatal hyperammonemia: activity of urea cycle enzymes.

L J Shapiro, M E Bocian, L Raijman, S D Cederbaum, K N Shaw.   

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Year:  1978        PMID： 31423     DOI： 10.1016/s0022-3476(78)81230-x

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


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  3 in total

1.  Evaluation of branched-chain amino acid intake in children with maple syrup urine disease and methylmalonic aciduria.

Authors:  H G Parsons; R J Carter; M Unrath; F F Snyder
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Megavitamin therapy in inherited metabolic disorders.

Authors:  S C Kalhan
Journal:  Indian J Pediatr       Date:  1981 Sep-Oct       Impact factor: 1.967

3.  Dietary therapy in two patients with vitamin B12-unresponsive methylmalonic acidemia.

Authors:  T Satoh; K Narisawa; Y Igarashi; T Saitoh; K Hayasaka; Y Ichinohazama; H Onodera; K Tada; K Oohara
Journal:  Eur J Pediatr       Date:  1981-02       Impact factor: 3.183
  3 in total

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