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Kidney International|April 29, 1998
Genetic studies into inherited and sporadic hemolytic uremic syndromeP Warwicker, T H Goodship, R L Donne, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|May 27, 1999
Familial relapsing haemolytic uraemic syndrome and complement factor H deficiencyP Warwicker, R L Donne, J A Goodship, et al.American Journal of Human Genetics|March 31, 2000
Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1S A Feather, S Malcolm, A S Woolf, et al.Prenatal Diagnosis|October 1, 1996
Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardationA L Webb, S Sturgiss, P Warwicker, et al.American Journal of Human Genetics|February 15, 2001
Factor H mutations in hemolytic uremic syndrome cluster in exons 18-20, a domain important for host cell recognitionA Richards, M R Buddles, R L Donne, et al.QJM : Monthly Journal of the Association of Physicians|February 9, 2002
Acute renal failure and metabolic disturbances in the short bowel syndromeA Banerjee, P WarwickerKidney International. Supplement|December 1, 1994
Acid-base regulation in peritoneal dialysisK A Graham, D Reaich, T H GoodshipKidney International. Supplement|January 14, 2000
Acidosis and nutritionJ D Louden, R R Roberts, T H GoodshipSeminars in Dialysis|August 3, 2000
What have isotope studies in humans told us about the nutritional effects of acidosis in dialysis?J D Louden, R G Roberts, T H GoodshipThe Annals of Thoracic Surgery|March 28, 2001
Nutritional status of patients undergoing lung cancer operationsR T Jagoe, T H Goodship, G J GibsonPageof 8