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Pediatric Nephrology (Berlin, Germany)|December 20, 2003
Renal replacement therapy in children: data from 12 registries in EuropeBert J van der Heijden, Paul C W van Dijk, Kate Verrier-Jones, et al.Kidney International|March 23, 2005
Renal replacement therapy for diabetic end-stage renal disease: data from 10 registries in Europe (1991-2000)Paul C W Van Dijk, Kitty J Jager, Bénédicte Stengel, et al.European Journal of Cell Biology|January 1, 1985
Detection of different cellular sides in rat liver and kidney by two monoclonal antibodies raised against the nucleotide-sugar hydrolyzing enzymes phosphodiesterase I and CMP-sialic acid hydrolaseW van Dijk, H G Muilerman, H G ter Hart, et al.Biology of Reproduction|February 28, 2003
Cloning and spatiotemporal expression of the follicle-stimulating hormone beta subunit complementary DNA in the African catfish (Clarias gariepinus)H F Vischer, A C C Teves, J C M Ackermans, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1994
Chronic idiopathic axonal polyneuropathy: a five year follow upN C Notermans, J H Wokke, Y van der Graaf, et al.Nederlands Tijdschrift Voor Geneeskunde|April 29, 1998
[Referral of patients with polyneuropathy by the family physician: influence of type of symptoms but not of age]G W van Dijk, N C Notermans, Y van der Graaf, et al.Journal of Neurology|September 26, 2006
Interobserver agreement and predictive value for outcome of two rating scales for the amount of extravasated blood after aneurysmal subarachnoid haemorrhageAnouk G W van Norden, Gert W van Dijk, Marc D van Huizen, et al.Clinical Science (London, England : 1979)|January 1, 1994
Heterogeneity of human biliary mucin: functional implicationsJ H Klinkspoor, M J van Wijland, C A Koeleman, et al.Journal of Medical Genetics|June 14, 2008
Prevalence and heritability of the metabolic syndrome and its individual components in a Dutch isolate: the Erasmus Rucphen Family studyP Henneman, Y S Aulchenko, R R Frants, et al.Annals of the Rheumatic Diseases|July 17, 2001
Specific glycosylation of alpha(1)-acid glycoprotein characterises patients with familial Mediterranean fever and obligatory carriers of MEFVD C Poland, J P Drenth, E Rabinovitz, et al.Pageof 34