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1. Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group

5. Sex, Genotype, and Liver Volume Progression as Risk of Hospitalization Determinants in Autosomal Dominant Polycystic Liver Disease

9. Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease

12. Bone health in autosomal dominant polycystic kidney disease (ADPKD) patients after kidney transplantation

13. Clinical Implementation of an Artificial Intelligence Algorithm for Magnetic Resonance–Derived Measurement of Total Kidney Volume

14. The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene Project

15. Cardiovascular Outcomes in Kidney Transplant Recipients With ADPKD

16. Monoallelic pathogenic ALG5 variants cause atypical polycystic kidney disease and interstitial fibrosis

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

21. Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype

22. Risk Severity Model for Pediatric Autosomal Dominant Polycystic Kidney Disease Using 3D Ultrasound Volumetry

24. Activation of PIEZO1 Inhibits Kidney Cystogenesis

25. Sex, Genotype, and Liver Volume Progression as Risk of Hospitalization Determinants in Autosomal Dominant Polycystic Liver Disease

26. Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease

27. Genomics Integration Into Nephrology Practice

35. Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group

38. The genetic landscape of polycystic kidney disease in Ireland

39. Genomic diagnostics in polycystic kidney disease: an assessment of real-world use of whole-genome sequencing

42. Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease

44. Detection and characterization of mosaicism in autosomal dominant polycystic kidney disease

49. Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohorts

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