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Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|August 3, 2021
[Molecular medicine: pathobiochemistry as the key to personalized treatment of inherited diseases]J A Mayr, R G Feichtinger, M T Achleitner, et al.
JIMD Reports|June 5, 2013
Socio-emotional Problems in Children with CDGK F E van de Loo, L van Dongen, M Mohamed, et al.
Neurology|September 22, 2010
3-Methylglutaconic aciduria type I redefined: a syndrome with late-onset leukoencephalopathyS B Wortmann, B H Kremer, A Graham, et al.
Biochimica Et Biophysica Acta|March 3, 2011
Clinical and diagnostic approach in unsolved CDG patients with a type 2 transferrin patternM Mohamed, M Guillard, S B Wortmann, et al.
Orphanet Journal of Rare Diseases|April 29, 2019
The natural history of classic galactosemia: lessons from the GalNet registryM E Rubio-Gozalbo, M Haskovic, A M Bosch, et al.
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