Literature DB >> 5677482

Hereditary orotic aciduria. I. A new case with family studies.

L E Rogers, L R Warford, R B Patterson, F S Porter.   

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Year:  1968        PMID： 5677482

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  5 in total

1.  Megaloblastic anemia--a rare cause.

Authors:  Sanjib Kr Debnath; Anju Aggarwal; Hema Mittal
Journal:  Indian J Pediatr       Date:  2011-06-01       Impact factor: 1.967

2.  Hereditary orotic aciduria: evidence for a structural gene mutation.

Authors:  T E Worthy; W Grobner; W N Kelley
Journal:  Proc Natl Acad Sci U S A       Date:  1974-08       Impact factor: 11.205

Review 3.  Folate deficiency in premature infants.

Authors:  A V Hoffbrand
Journal:  Arch Dis Child       Date:  1970-08       Impact factor: 3.791

4.  Activity of orotate metabolizing enzyme complex and various urea-cycle enzymes in mutant mice with ornithine transcarbamylase deficiency.

Authors:  I A Qureshi; J Letarte; R Ouellet
Journal:  Experientia       Date:  1982-03-15

5.  Mechanism of allopurinol-mediated increase in enzyme activity in man.

Authors:  T D Beardmore; J S Cashman; W N Kelley
Journal:  J Clin Invest       Date:  1972-07       Impact factor: 14.808
  5 in total

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