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Nature Reviews. Nephrology|October 10, 2017
New treatment paradigms for ADPKD: moving towards precision medicineMatthew B Lanktree, Arlene B ChapmanCanadian Journal of Kidney Health and Disease|February 19, 2024
Large Kidney Cysts in <i>HNF1B</i> Nephropathy Mimicking Autosomal Dominant Polycystic Kidney DiseaseNada Alamri, Matthew B LanktreeJournal of the American Society of Nephrology : JASN|April 13, 2007
Autosomal dominant polycystic kidney disease: time for a change?Arlene B ChapmanClinical Journal of the American Society of Nephrology : CJASN|June 27, 2008
Approaches to testing new treatments in autosomal dominant polycystic kidney disease: insights from the CRISP and HALT-PKD studiesArlene B ChapmanKidney International|February 4, 2014
The importance of quantifying genetic heterogeneity in ADPKDArlene B ChapmanAdvances in Renal Replacement Therapy|March 5, 2003
Cystic disease in women: clinical characteristics and medical managementArlene B ChapmanKidney International|April 14, 2012
The fetal environment: a critical phase that determines future renal outcomes in autosomal dominant polycystic kidney diseaseArlene B ChapmanKidney International|January 1, 2009
Improving clinical trial design for inquiries into the mechanisms of cyst growth in ADPKDArlene B ChapmanGenome Medicine|April 4, 2009
Gene-gene and gene-environment interactions: new insights into the prevention, detection and management of coronary artery diseaseMatthew B Lanktree, Robert A HegelePageof 28