N. G. G. M. Abeling

Brown‐Vialetto‐Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatment

Annet M. Bosch, N. G. G. M. Abeling, Lodewijk IJlst et al. · Journal of Inherited Metabolic Disease · 2010 · 240 citations · Full text

Plasma and Erythrocyte Fatty Acid Patterns in Patients with Recurrent Depression: A Matched Case-Control Study

Johanna Assies, Anja Lok, Roel J. T. Mocking et al. · PLoS ONE · 2010 · 126 citations · Full text

Etiology of Mental Retardation in Children Referred to a Tertiary Care Center: A Prospective Study

Clara van Karnebeek, Frederike Y. Scheper, N. G. G. M. Abeling et al. · American Journal on Mental Retardation · 2005 · 109 citations

Disability, Diagnosis, Education +26

β-Ureidopropionase deficiency: an inborn error of pyrimidine degradation associated with neurological abnormalities

André B. P. Kuilenburg, Rutger Meinsma, Eva Beke et al. · Human Molecular Genetics · 2004 · 87 citations

Genetics, Molecular Biology, Escherichia Coli +16

Catecholamines profiles at diagnosis: Increased diagnostic sensitivity and correlation with biological and clinical features in neuroblastoma patients

I.R.N. Verly, André B. P. Kuilenburg, N. G. G. M. Abeling et al. · European Journal of Cancer · 2017 · 73 citations

Neuro-oncology, Neuroblastoma Patients, Neuroblasts +6