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Nephron. Clinical Practice|October 23, 2004
Aetiological factors in paediatric urolithiasisWilliam G van't HoffPediatric Nephrology (Berlin, Germany)|May 8, 2003
Neonatal nephrocalcinosis in association with glucose-galactose malabsorptionAmitava Pahari, Peter J Milla, William G van't HoffPediatric Nephrology (Berlin, Germany)|May 17, 2003
Nephrocalcinosis and medullary cysts in 3-methylglutaconic aciduriaGuido F Laube, James V Leonard, William G van't HoffPediatric Nephrology (Berlin, Germany)|January 1, 2005
Exfoliated human proximal tubular cells: a model of cystinosis and Fanconi syndromeGuido F Laube, Mushfequr R Haq, William G van't HoffUrological Research|March 14, 2009
Primary cultures of renal proximal tubule cells derived from individuals with primary hyperoxaluriaKaren L Price, Sally-Anne Hulton, William G van't Hoff, et al.Pediatric Nephrology (Berlin, Germany)|June 9, 2005
Childhood thin GBM disease: review of 22 children with family studies and long-term follow-upCarla Carasi, William G Van't Hoff, Lesley Rees, et al.European Journal of Pediatrics|July 9, 2004
Neonatal severe hyperparathyroidism: genotype/phenotype correlation and the use of pamidronate as rescue therapySimon Waller, Tom Kurzawinski, Lewis Spitz, et al.Journal of the American Society of Nephrology : JASN|July 26, 2002
Immunolocalization of cystinosin, the protein defective in cystinosisMushfequr R Haq, Vasiliki Kalatzis, Marie-Claire Gubler, et al.Pediatric Nephrology (Berlin, Germany)|February 12, 2017
Clinical and molecular aspects of distal renal tubular acidosis in childrenMartine T P Besouw, Marc Bienias, Patrick Walsh, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 7, 2012
The enzyme 4-hydroxy-2-oxoglutarate aldolase is deficient in primary hyperoxaluria type 3Emma L Williams, Detlef Bockenhauer, William G van't Hoff, et al.Pageof 2