1,157 results on '"Harris, Peter C."'
Search Results
2. Biomarkers of Kidney Disease Progression in ADPKD
3. DNA methyltransferase 1 (DNMT1) promotes cyst growth and epigenetic age acceleration in autosomal dominant polycystic kidney disease
4. Association of Kidney Cysts With Progressive CKD After Radical Nephrectomy
5. Sex, Genotype, and Liver Volume Progression as Risk of Hospitalization Determinants in Autosomal Dominant Polycystic Liver Disease
6. How We Treat Primary Hyperoxaluria Type 1
7. Polygenic risk alters the penetrance of monogenic kidney disease
8. State of the Science and Ethical Considerations for Preimplantation Genetic Testing for Monogenic Cystic Kidney Diseases and Ciliopathies
9. Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease
10. Genetic Spectrum of Polycystic Kidney and Liver Diseases and the Resulting Phenotypes
11. The Site and Type of CLCN5 Genetic Variation Impact the Resulting Dent Disease-1 Phenotype
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
17. The genetics of kidney stone disease and nephrocalcinosis
18. Genetics in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
19. Netrin-1 Overexpression Induces Polycystic Kidney Disease: A Novel Mechanism Contributing to Cystogenesis in Autosomal Dominant Polycystic Kidney Disease
20. Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case Series
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
23. Clinical and molecular characterization of primary hyperoxaluria in Egypt
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
28. Primary results of the randomized trial of metformin administration in polycystic kidney disease (TAME PKD)
29. Pain and Obesity in Autosomal Dominant Polycystic Kidney Disease: A Post Hoc Analysis of the Halt Progression of Polycystic Kidney Disease (HALT-PKD) Studies
30. High Prevalence of Kidney Cysts in Patients With CYP24A1 Deficiency
31. The genetic background significantly impacts the severity of kidney cystic disease in the Pkd1RC/RC mouse model of autosomal dominant polycystic kidney disease
32. Up-Regulation of DNA Damage Response Signaling in Autosomal Dominant Polycystic Kidney Disease
33. Biallelic inheritance of hypomorphic PKD1 variants is highly prevalent in very early onset polycystic kidney disease
34. Prognostic Value of Fibroblast Growth Factor 23 in Autosomal Dominant Polycystic Kidney Disease
35. Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group
36. Semantic Instance Segmentation of Kidney Cysts in MR Images: A Fully Automated 3D Approach Developed Through Active Learning
37. Characteristics of Patients with End-Stage Kidney Disease in ADPKD
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
40. Epidemiology of autosomal-dominant polycystic liver disease in Olmsted county
41. Regulation of polycystin expression, maturation and trafficking
42. Clinical spectrum, prognosis and estimated prevalence of DNAJB11-kidney disease
43. Cl− and H+ coupling properties and subcellular localizations of wildtype and disease-associated variants of the voltage-gated Cl−/H+ exchanger ClC-5
44. Detection and characterization of mosaicism in autosomal dominant polycystic kidney disease
45. Overexpression of SMYD3 Promotes Autosomal Dominant Polycystic Kidney Disease by Mediating Cell Proliferation and Genome Instability
46. Combining genotype with height-adjusted kidney length predicts rapid progression of ADPKD
47. PKD1 Truncating Mutations Accelerate eGFR Decline in Autosomal Dominant Polycystic Kidney Disease Patients
48. Protein Kinase A Downregulation Delays the Development and Progression of Polycystic Kidney Disease
49. Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohorts
50. CYP24A1 deficiency causing persistent hypercalciuria in a stone former
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