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Emergency management of inherited metabolic diseases.
Prietsch V, Lindner M, Zschocke J, Nyhan WL, Hoffmann GF. Prietsch V, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2002 Nov;25(7):531-46. doi: 10.1023/a:1022040422590. J Inherit Metab Dis. 2002. PMID: 12638937 Review.
Neonatal screening for glutaryl-CoA dehydrogenase deficiency.
Lindner M, Kölker S, Schulze A, Christensen E, Greenberg CR, Hoffmann GF. Lindner M, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2004;27(6):851-9. doi: 10.1023/B:BOLI.0000045769.96657.af. J Inherit Metab Dis. 2004. PMID: 15505392 Review.
Emergency treatment in glutaryl-CoA dehydrogenase deficiency.
Kölker S, Greenberg CR, Lindner M, Müller E, Naughten ER, Hoffmann GF. Kölker S, et al. Among authors: hoffmann gf. J Inherit Metab Dis. 2004;27(6):893-902. doi: 10.1023/B:BOLI.0000045774.51260.ea. J Inherit Metab Dis. 2004. PMID: 15505397 Review.
614 results