524 results on '"Goodyer, Paul"'
Search Results
2. Tubular Diseases and Stones Seen From Pediatric and Adult Nephrology Perspectives
3. Clinical Use of Diuretics
4. Congenital Anomalies of the Kidneys
5. Wilms’ tumor gene 1: lessons from the interface between kidney development and cancer
6. A no-nonsense approach to hereditary kidney disease
7. Congenital Anomalies of the Kidneys
8. Clinical Use of Diuretics
9. Nephropathic cystinosis: an international consensus document
10. Wilms' tumor gene 1: lessons from the interface between kidney development and cancer.
11. The Québec NTBC Study
12. The aminoglycoside geneticin permits translational readthrough of the CTNS W138X nonsense mutation in fibroblasts from patients with nephropathic cystinosis
13. Use of genomic and functional analysis to characterize patients with steroid-resistant nephrotic syndrome
14. Tubular Disorders
15. Evaluation of Renal Disease
16. Renal Transplantation
17. Renal Dysplasia/Hypoplasia
18. Expanding the phenotypic spectrum of CC2D2A-related ciliopathies: a rare homozygous nonsense variant in a patient with suspected nephronophthisis
19. Unraveling the natural history of presymptomatic cystinuria
20. Transition From Pediatric to Adult Nephrology Care: Program Report of a Single-Center Experience
21. Studies in the design and development of miniature optical-fibre in-vivo sensors : with applications in obstructive sleep apnoea syndrome and arterial restenosis
22. WT1 regulates expression of DNA-repair gene Neil3 during nephrogenesis
23. A Physiologic Approach to Hereditary Tubulopathies
24. Renal Dysplasia/Hypoplasia
25. WT1 regulates expression of DNA repair gene Neil3 during nephrogenesis.
26. Nephron progenitor cells in development and disease
27. Contributors
28. Genetic and Epigenetic Regulation of Nephron Number in the Human
29. Renal Dysplasia/Hypoplasia
30. Kidney/ear syndromes
31. Priming the renal progenitor cell
32. Caring for people in the field
33. Expression of Growth-Related Genes in Human Fetal Kidney
34. Hereditary Tubular Transport Abnormalities
35. WT1 regulates expression of DNA repair gene Neil3during nephrogenesis
36. Urinary monocyte chemoattractant protein-1 and hepcidin and early diabetic nephropathy lesions in type 1 diabetes mellitus
37. TNFα pathway blockade ameliorates toxic effects of FSGS plasma on podocyte cytoskeleton and β3 integrin activation
38. Plasma from a case of recurrent idiopathic FSGS perturbs non-muscle myosin IIA (MYH9 protein) in human podocytes
39. Photoelectron spectroscopy of dithiolatodiironhexacarbonyl models for the active site of [Fe–Fe] hydrogenases: Insight into the reorganization energy of the “rotated” structure in the enzyme
40. In vivo validation of PAX2 as a target for renal cancer therapy
41. Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn
42. Renal and retinal effects of enalapril and losartan in type 1 diabetes
43. Phase 1 Renal Impairment Trial Results Supports Targeted Individualized Dosing of ELX‐02 in Patients With Nephropathic Cystinosis
44. Effects of maternal vitamin A status on kidney development: a pilot study
45. Endolymphatic Sac Enlargement in a Girl with a Novel Mutation for Distal Renal Tubular Acidosis and Severe Deafness
46. Renal hypoplasia: lessons from Pax2
47. LGL1, a novel branching morphogen in developing kidney, is induced by retinoic acid
48. Canonical WNT signaling during kidney development
49. PAX2 is reactivated in urinary tract obstruction and partially protects collecting duct cells from programmed cell death
50. Renal Transplantation
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