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2. Increased risk of kidney failure in patients with genetic kidney disorders

6. Association of COVID-19 Versus COVID-19 Vaccination With Kidney Function and Disease Activity in Primary Glomerular Disease: A Report of the Cure Glomerulonephropathy Study

8. The Significance of Hematuria in Podocytopathies

9. Reopening Schools Safely: The Case for Collaboration, Constructive Disruption of Pre-Coronavirus 2019 Expectations, and Creative Solutions.

11. Racial and Ethnic Disparities in Acute Care Utilization Among Patients With Glomerular Disease

12. Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

15. Association of Obesity With Kidney and Cardiac Outcomes Among Patients With Glomerular Disease: Findings From the Cure Glomerulonephropathy Network

17. Improving data quality in observational research studies: Report of the Cure Glomerulonephropathy (CureGN) network

19. Longitudinal Changes in Health-Related Quality of Life in Primary Glomerular Disease: Results From the CureGN Study

20. CTSA Consortium Consensus Scientific Review Committee (SRC) Working Group Report on the SRC Processes

22. Consensus Expert Recommendations for the Diagnosis and Management of Autosomal Recessive Polycystic Kidney Disease: Report of an International Conference

25. Differential regulation of MYC expression by PKHD1/Pkhd1 in human and mouse kidneys: phenotypic implications for recessive polycystic kidney disease

27. List of Contributors

31. Racial and Ethnic Disparities in Acute Care Utilization Among Patients With Glomerular Disease

33. Age of Onset and Disease Course in Biopsy-Proven Minimal Change Disease: An Analysis From the Cure Glomerulopathy Network

36. Pkhd1cyli/cyli mice have altered renal Pkhd1 mRNA processing and hormonally sensitive liver disease.

39. Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

41. Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2

42. Clinical and genetic characterization of a founder PKHD1 mutation in Afrikaners with ARPKD

43. Cystin is required for maintaining fibrocystin (FPC) levels and safeguarding proteome integrity in mouse renal epithelial cells A mechanistic connection between the kidney defects incpkmice and human ARPKD

44. Additional file 3 of Validation of a computational phenotype for finding patients eligible for genetic testing for pathogenic PTEN variants across three centers

45. Additional file 4 of Validation of a computational phenotype for finding patients eligible for genetic testing for pathogenic PTEN variants across three centers

46. Expanding the phenotype of proteinuria in dent disease. A case series

47. Neurocognition in children with autosomal recessive polycystic kidney disease in the CKiD cohort study

49. Contributors

50. Contributors

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