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G F Hoffmann

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Journal of Inherited Metabolic Disease|July 1, 1997

Phosphomannomutase deficiency is the main cause of carbohydrate-deficient glycoprotein syndrome with type I isoelectrofocusing pattern of serum sialotransferrinsJ Jaeken, J Artigas, R Barone, et al.

Annals of Neurology|January 23, 1999

D-2-Hydroxyglutaric aciduria: biochemical marker or clinical disease entity?M S van der Knaap, C Jakobs, G F Hoffmann, et al.

Journal of Inherited Metabolic Disease|January 5, 2007

Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)S Kölker, E Christensen, J V Leonard, et al.

Neurology|May 28, 2010

Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiencyL Brun, L H Ngu, W T Keng, et al.

Pageof 22

Search research articles

Showing results (211-220 of 214) with videos related to

Sort By:

Pageof 22

You have reached the last page of results.This site can display upto 214 results.

Journal of Inherited Metabolic Disease|July 1, 1997

Phosphomannomutase deficiency is the main cause of carbohydrate-deficient glycoprotein syndrome with type I isoelectrofocusing pattern of serum sialotransferrinsJ Jaeken, J Artigas, R Barone, et al.

Annals of Neurology|January 23, 1999

D-2-Hydroxyglutaric aciduria: biochemical marker or clinical disease entity?M S van der Knaap, C Jakobs, G F Hoffmann, et al.

Journal of Inherited Metabolic Disease|January 5, 2007

Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)S Kölker, E Christensen, J V Leonard, et al.

Neurology|May 28, 2010

Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiencyL Brun, L H Ngu, W T Keng, et al.

Pageof 22