J
J. Williamson Balfe
Researcher at University of Toronto
Publications - 31
Citations - 1299
J. Williamson Balfe is an academic researcher from University of Toronto. The author has contributed to research in topics: Peritoneal dialysis & Renal function. The author has an hindex of 21, co-authored 31 publications receiving 1275 citations. Previous affiliations of J. Williamson Balfe include Hospital for Sick Children.
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Journal ArticleDOI
Indomethacin and renal function in premature infants with persistent patent ductus arteriosus
TL;DR: Renal function during indomethacin treatment was studied in premature infants with patent ductus arteriosus, and except for GFR and urinary Na and osmolality, all these functions returned to pretreatment values one to two weeks after stopping the drug.
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The use of capd in the treatment of children with end-stage renal disease
TL;DR: The prognosis for a successful renal transplant in children with Wilms' tumor is poor; they frequently die of sepsis or tumor recurrence and the longer the interval between the cure of the malignancy and the transplantation, the better the post-transplant results.
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Angiotensin converting enzyme inhibitor therapy to decrease microalbuminuria in normotensive children with insulin-dependent diabetes mellitus.
Jennifer Cook,Denis Daneman,Michael Spino,Etienne Sochett,Kusiel Perlman,J. Williamson Balfe +5 more
TL;DR: It is concluded that, in the short term, captopril is effective in decreasing albumin excretion rate in normotensive children with insulin-dependent diabetes mellitus and microalbuminuria, without significant side effects.
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Acetoacetyl CoA thiolase deficiency: A cause of severe ketoacidosis in infancy simulating salicylism
Brian H. Robinson,W. Geoffrey Sherwood,Jennifer A. Taylor,J. Williamson Balfe,Orval A. Mamer +4 more
TL;DR: Evidence is presented that beta-ketothiolase deficiency is not simply a defect of isoleucine degradation; the deficient enzyme is the K+ dependent short-chain mitochondrial thiolase, which also plays a major catalytic role in ketone body and fatty acid oxidation.
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Diagnosis and management of stenotic aorto-arteriopathy in childhood
Sudhir J.A. D'Souza,Wen-Shiung Tsai,Meredith M. Silver,Peter Chait,Lee N. Benson,Earl D. Silverman,Diane Hebert,J. Williamson Balfe +7 more
TL;DR: Distinguishing SAA resulting from fibromuscular dysplasia caused by Takayasu arteritis in the chronic vaso-occlusive phase may be unnecessary for effective treatment, and therapy should focus on interventions to minimize the end-organ damage caused by the vasiocclusive manifestations of the disorders.