Showing results (41-50 of 529) with videos related to

Sort By:
Pageof 53
Journal of Inherited Metabolic Disease|January 1, 1985
Pipecolic acid levels in serum and urine from neonates and normal infants: comparison with values reported in Zellweger syndromeL Govaerts, F Trijbels, L Monnens, et al.
Tijdschrift Voor Kindergeneeskunde|April 1, 1986
[The enlarged kidney in infancy--echographic findings]J M Cobben, C Boetes, J de Vries, et al.
Nephron|January 1, 1979
Development of glomerular fibrinolytic activity in the ratL Monnens, P van Wieringen, I Lambooy, et al.
Tijdschrift Voor Kindergeneeskunde|April 1, 1983
[A child with Zellweger's cerebrohepatorenal syndrome]L Govaerts, J Corstiaensen, J Bakkeren, et al.
Human Mutation|April 17, 2008
Bottlenecks in molecular testing for rare genetic diseasesPatrick J Willems
Nephron|January 1, 1981
DDAVP test for assessment of renal concentrating capacity in infants and childrenL Monnens, Y Smulders, H van Lier, et al.
Tijdschrift Voor Kindergeneeskunde|June 1, 1993
[2 children with stridor and a thymus in the posterior mediastinum]P W van Mossevelde, R Severijnen, C Hitge-Boetes, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|May 14, 2005
ACTH, alpha-MSH, and control of cortisol release: cloning, sequencing, and functional expression of the melanocortin-2 and melanocortin-5 receptor in Cyprinus carpioJuriaan R Metz, Edwin J W Geven, Erwin H van den Burg, et al.
Tijdschrift Voor Kindergeneeskunde|April 1, 1986
[Echography of the normal kidney in infants]J M Cobben, H Jansen, C Boetes, et al.
Human Genetics|November 19, 2002
Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2)L P van den Heuvel, K Assink, M Willemsen, et al.
Pageof 53