Ference J. Loupatty

Enzymology of the branched‐chain amino acid oxidation disorders: the valine pathway

Ronald J. A. Wanders, Marinus Durán, Ference J. Loupatty · Journal of Inherited Metabolic Disease · 2010 · 91 citations · Full text

Biosynthesis, Cellular Enzymology, Biochemistry +14

Mutations in the Gene Encoding 3-Hydroxyisobutyryl-CoA Hydrolase Results in Progressive Infantile Neurodegeneration

Ference J. Loupatty, Peter T. Clayton, Jos P.N. Ruiter et al. · The American Journal of Human Genetics · 2006 · 84 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +8

Multicenter comparison study of current methods to measure 25-hydroxyvitamin D in serum

Marcel J.W. Janssen, Jos P.M. Wielders, Corinne C. Bekker et al. · Steroids · 2012 · 79 citations

Medicine, Bioanalysis, Clinical Nutrition +5

3-Methylglutaconic Aciduria Type I Is Caused by Mutations in AUH

Lodewijk IJlst, Ference J. Loupatty, Jos P.N. Ruiter et al. · The American Journal of Human Genetics · 2002 · 73 citations · Full text

Urology, Somatic Variant, Autoimmune Disease +10

Can serum L-lactate, D-lactate, creatine kinase and I-FABP be used as diagnostic markers in critically ill patients suspected for bowel ischemia

Peter HJ van der Voort, Berit Westra, J. P. J. Wester et al. · BMC Anesthesiology · 2014 · 63 citations · Full text