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Nature Reviews. Nephrology|December 21, 2011
Genetic determinants of urolithiasisCarla G Monico, Dawn S MillinerAmerican Journal of Nephrology|April 26, 2005
Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluriaCarla G Monico, Julie B Olson, Dawn S MillinerKidney International|April 21, 2005
Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant alleleCarla G Monico, Sandro Rossetti, Julie B Olson, et al.Kidney International|July 12, 2002
Potential mechanisms of marked hyperoxaluria not due to primary hyperoxaluria I or IICarla G Monico, Mai Persson, G Charles Ford, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 7, 2006
Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2John Knight, Ross P Holmes, Dawn S Milliner, et al.Circulation Journal : Official Journal of the Japanese Circulation Society|October 6, 2010
Cardiac abnormalities in primary hyperoxaluriaFarouk Mookadam, Travis Smith, Panupong Jiamsripong, et al.Acta Paediatrica (Oslo, Norway : 1992). Supplement|June 28, 2006
Stones, bones, and heredityDawn S MillinerAmerican Journal of Nephrology|April 28, 2005
The primary hyperoxalurias: an algorithm for diagnosisDawn S MillinerJournal of the American Society of Nephrology : JASN|April 27, 2007
Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosisCarla G Monico, Sandro Rossetti, Heidi A Schwanz, et al.American Journal of Nephrology|June 18, 2005
International registry for primary hyperoxaluriaJohn C Lieske, Carla G Monico, W Scott Holmes, et al.Pageof 8