Literature DB >> 6687844

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

E Christensen.   

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Year:  1983        PMID： 6687844     DOI： 10.1016/0009-8981(83)90155-9

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


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  22 in total

1.  Glutaric aciduria type I: pathomechanisms of neurodegeneration.

Authors:  K Ullrich; B Flott-Rahmel; P Schluff; U Musshoff; A Das; T Lücke; R Steinfeld; E Christensen; C Jakobs; A Ludolph; A Neu; R Röper
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

2.  Glutaric aciduria and suspected child abuse.

Authors:  A A Morris; G F Hoffmann; E R Naughten; A A Monavari; J E Collins; J V Leonard
Journal:  Arch Dis Child       Date:  1999-05       Impact factor: 3.791

3.  Significance of bound glutarate in the diagnosis of glutaric aciduria type I.

Authors:  A Ribes; E Riudor; P Briones; E Christensen; J Campistol; D S Millington
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

4.  Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management.

Authors:  A A Monavari; E R Naughten
Journal:  Arch Dis Child       Date:  2000-01       Impact factor: 3.791

5.  Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).

Authors:  S Kölker; E Christensen; J V Leonard; C R Greenberg; A B Burlina; A P Burlina; M Dixon; M Duran; S I Goodman; D M Koeller; E Müller; E R Naughten; E Neumaier-Probst; J G Okun; M Kyllerman; R A Surtees; B Wilcken; G F Hoffmann; P Burgard
Journal:  J Inherit Metab Dis       Date:  2007-01-03       Impact factor: 4.982

6.  The segregation of glutaryl-CoA dehydrogenase deficiency and Refsum syndrome in a family.

Authors:  E Christensen; N J Brandt; T Rosenberg; K Bömers; C Jakobs
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

7.  Compound heterozygosity in the glutaryl-CoA dehydrogenase gene with R227P mutation in one allele is associated with no or very low free glutarate excretion.

Authors:  E Christensen; A Ribes; C Busquets; M Pineda; M Duran; B T Poll-The; C R Greenberg; H Leffers; M Schwartz
Journal:  J Inherit Metab Dis       Date:  1997-07       Impact factor: 4.982

8.  Nerve cell lesions caused by 3-hydroxyglutaric acid: a possible mechanism for neurodegeneration in glutaric acidaemia I.

Authors:  B Flott-Rahmel; C Falter; P Schluff; R Fingerhut; E Christensen; C Jakobs; U Musshoff; J D Fautek; T Deufel; A Ludolph; K Ullrich
Journal:  J Inherit Metab Dis       Date:  1997-07       Impact factor: 4.982

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

Authors:  E Christensen
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

10.  Prolidase deficiency: it looks like systemic lupus erythematosus but it is not.

Authors:  Aharon Klar; Paulina Navon-Elkan; Alan Rubinow; David Branski; Haggit Hurvitz; Ernst Christensen; Morad Khayat; Tzipora C Falik-Zaccai
Journal:  Eur J Pediatr       Date:  2009-11-24       Impact factor: 3.183
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