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European Journal of Pediatrics|March 1, 1991
A variant of nephrogenic diabetes insipidus: V2 receptor abnormality restricted to the kidneyN Knoers, L A MonnensPediatric Nephrology (Berlin, Germany)|September 1, 1992
Nephrogenic diabetes insipidus: clinical symptoms, pathogenesis, genetics and treatmentN Knoers, L A MonnensTijdschrift Voor Kindergeneeskunde|February 1, 1987
[Neonatal ascites caused by urine leakage]N Knoers, L Monnens, J de VriesEuropean Journal of Pediatrics|May 1, 1992
Evidence for intact V1-vasopressin receptors in congenital nephrogenic diabetes insipidusN Knoers, P M Janssens, J Goertz, et al.European Journal of Pediatrics|September 18, 2007
Growth charts for Wolf-Hirschhorn syndrome (0-4 years of age)T Antonius, J Draaisma, E Levtchenko, et al.Clinical Neurology and Neurosurgery|June 24, 1998
Genetic and environmental risk factors in Parkinson's diseaseB A Veldman, A M Wijn, N Knoers, et al.Nephron|January 1, 1990
Fibrinolytic responses to 1-desamino-8-D-arginine-vasopressin in patients with congenital nephrogenic diabetes insipidusN Knoers, E J Brommer, H Willems, et al.Prostaglandins, Leukotrienes, and Essential Fatty Acids|April 1, 1990
Urinary excretion of prostaglandins during infancy and childhood: influence of age, sodium restriction and postureN Knoers, T Fiselier, C Thomas, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 24, 2001
Autosomal recessive hypophosphataemic rickets with hypercalciuria is not caused by mutations in the type II renal sodium/phosphate cotransporter geneL van den Heuvel, K Op de Koul, E Knots, et al.Nephron|January 1, 1988
Linkage of X-linked nephrogenic diabetes insipidus with DXS52, a polymorphic DNA markerN Knoers, H vd Heyden, B A von Oost, et al.Pageof 2