Literature DB >> 2512425

First trimester prenatal exclusion of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type 1).

E Christensen1.   

Abstract

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Year:  1989        PMID： 2512425     DOI： 10.1007/bf03335397

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  4 in total

1.  Glutaric aciduria; a "new" disorder of amino acid metabolism.

Authors:  S I Goodman; S P Markey; P G Moe; B S Miles; C C Teng
Journal:  Biochem Med       Date:  1975-01

2.  Improved assay of glutaryl-CoA dehydrogenase in cultured cells and liver: application to glutaric aciduria type I.

Authors:  E Christensen
Journal:  Clin Chim Acta       Date:  1983-03-28       Impact factor: 3.786

3.  Glutaric aciduria type I: clinical heterogeneity and neuroradiologic features.

Authors:  N Amir; O el-Peleg; R S Shalev; E Christensen
Journal:  Neurology       Date:  1987-10       Impact factor: 9.910

4.  Antenatal diagnosis of glutaric acidemia.

Authors:  S I Goodman; D A Gallegos; C J Pullin; B Halpern; R J Truscott; G Wise; B Wilcken; E D Ryan; D T Whelen
Journal:  Am J Hum Genet       Date:  1980-09       Impact factor: 11.025
  4 in total
  1 in total

1.  Macrocephaly, dystonia, and bilateral temporal arachnoid cysts: glutaric aciduria type 1.

Authors:  J F Martínez-Lage; C Casas; M A Fernández; A Puche; T Rodriguez Costa; M Poza
Journal:  Childs Nerv Syst       Date:  1994-04       Impact factor: 1.475
  1 in total

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