A. A. M. Haagen

Expanding the clinical spectrum of 3‐phosphoglycerate dehydrogenase deficiency

L. Tabatabaie, Leo W. J. Klomp, M. Estela Rubio‐Gozalbo et al. · Journal of Inherited Metabolic Disease · 2010 · 60 citations · Full text

Predictive DNA testing for multiple endocrine neoplasia 2: A therapeutic challenge of prophylactic thyroidectomy in very young children

L.W. Ernest van Heurn, C. Schaap, George Sie et al. · Journal of Pediatric Surgery · 1999 · 59 citations

Therapeutic Challenge, Endocrine Oncology, Predictive Dna +9

Accuracy of the Precision^® point-of-care ketone test examined by liquid chromatography tandem-mass spectrometry (LC-MS/MS) in the same fingerstick sample

Marcel J.W. Janssen, Ben H.E. Hendrickx, Carin D. Habets-van der Poel et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 2010 · 24 citations

Absence of increased succinylacetone in the urine of a child with hereditary tyrosinaemia type I

A. A. M. Haagen, M. Durán · Journal of Inherited Metabolic Disease · 1987 · 11 citations

Increased Succinylacetone, Urology, Hereditary Tyrosinaemia Type

Deletion of chromosome region 18q21.1 → 18q21.3 in a patient without clinical features of the 18q‐ phenotype

J.J.M. Engelen, Ute Moog, Jacobiene W. Weber et al. · American Journal of Medical Genetics Part A · 2003 · 10 citations