Long-term follow-up, neurological outcome and survival rate in 28 Nordic patients with glutaric aciduria type 1-Reference-Cited by-同舟云学术

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Long-term follow-up, neurological outcome and survival rate in 28 Nordic patients with glutaric aciduria type 1

Published:2004-05 Issue:3 Volume:8 Page:121-129
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Kyllerman Mårten,Skjeldal Ola,Christensen Ernst,Hagberg Gudrun,Holme Elisabeth,Lönnquist Tuula,Skov Liselotte,Rotwelt Terje,von Döbeln Ulrika

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference26 articles.

1. Glutaric aciduria a ‘new’ disorder of amino acid metabolism;Goodman;Biochem Med,1975

2. Glutaric aciduria type 1: from clinical, biochemical and molecular diversity to successful therapy;Hoffmann;J Inher Metab Dis,1999

3. Dystonia and dyskinesia in glutaric aciduria type 1: clinical heterogeneity and therapeutic considerations;Kyllerman;Mov disord,1994

4. Clinical course, early diagnosis, treatment and prevention of disease in glutaryl-CoA dehydrogenase deficiency;Hoffmann;Neuropediatrics,1996

5. Acute profound dystonia in infants with glutaric acidemia;Bergman;Pediatrics,1989

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