Decline of Acute Encephalopathic Crises in Children with Glutaryl-CoA Dehydrogenase Deficiency Identified by Newborn Screening in Germany-Reference-Cited by-同舟云学术

Decline of Acute Encephalopathic Crises in Children with Glutaryl-CoA Dehydrogenase Deficiency Identified by Newborn Screening in Germany

Published:2007-09 Issue:3 Volume:62 Page:357-363
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Kölker Stefan,Garbade Sven F,Boy Nikolas,Maier Esther M,Meissner Thomas,Mühlhausen Chris,Hennermann Julia B,Lücke Thomas,Häberle Johannes,Baumkötter Jochen,Haller Wolfram,Müller Edith,Zschocke Johannes,Burgard Peter,Hoffmann Georg F

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference33 articles.

1. Glutaric aciduria; A “new” disorder of amino acid metabolism

2. Neonatal screening for glutaryl-CoA dehydrogenase deficiency

3. Outcome of the First 3-Years of a DNA-Based Neonatal Screening Program for Glutaric Acidemia Type 1 in Manitoba and Northwestern Ontario, Canada

4. Type I glutaric aciduria, part 1: Natural history of 77 patients

5. Glutaryl-CoA dehydrogenase mutations in glutaric acidemia (type I): Review and report of thirty novel mutations

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