Showing results (1-10 of 2,003) with videos related to
Sort By:
Pageof 201
Tijdschrift Voor Kindergeneeskunde|February 1, 1987
[Neonatal ascites caused by urine leakage]N Knoers, L Monnens, J de VriesTijdschrift Voor Kindergeneeskunde|April 1, 1986
[The enlarged kidney in infancy--echographic findings]J M Cobben, C Boetes, J de Vries, 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.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.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.Human Genetics|September 1, 1988
Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosomeN Knoers, H van der Heyden, B A van Oost, et al.Genomics|April 1, 1989
Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidusN Knoers, H van der Heyden, B A van Oost, et al.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 MonnensMonatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|October 1, 1986
[Type III osteogenesis imperfecta associated with hypophosphatemic vitamin D-resistant rickets]D Menzel, L MonnensPageof 201