Inga Knudsen

Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Mutations Identified by MS/MS-Based Prospective Screening of Newborns Differ from Those Observed in Patients with Clinical Symptoms: Identification and Characterization of a New, Prevalent Mutation That Results in Mild MCAD Deficiency*

Brage Storstein Andresen, Steve F. Dobrowolski, Linda P. O’Reilly et al. · The American Journal of Human Genetics · 2001 · 232 citations · Full text

Clinical Symptoms, Mendelian Disorder, Prevalent Mutation +14

The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype?

Brage Storstein Andresen, Peter Bross, Szabolcs Udvari et al. · Human Molecular Genetics · 1997 · 122 citations · Full text

Isolated 2-Methylbutyrylglycinuria Caused by Short/Branched-Chain Acyl-CoA Dehydrogenase Deficiency: Identification of a New Enzyme Defect, Resolution of Its Molecular Basis, and Evidence for Distinct Acyl-CoA Dehydrogenases in Isoleucine And Valine Metabolism

Brage Storstein Andresen, Ernst Christensen, Thomas J. Corydon et al. · The American Journal of Human Genetics · 2000 · 82 citations · Full text

New Enzyme Defect, Biosynthesis, Aldo-keto Reductase +9

Human ClpP protease: cDNA sequence, tissue‐specific expression and chromosomal assignment of the gene

Peter Bross, Brage Storstein Andresen, Inga Knudsen et al. · FEBS Letters · 1995 · 58 citations · Full text

The mutational spectrum in very long‐chain acyl‐CoA dehydrogenase deficiency

Brage Storstein Andresen, Christine Vianey‐Saban, Peter Bross et al. · Journal of Inherited Metabolic Disease · 1996 · 40 citations