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1. Preface

2. Contents

11. Notes

12. Index

16. Back Cover

17. Community-centered journalism : engaging people, exploring solutions, and building trust.

19. Long-read sequencing identifies a common transposition haplotype predisposing for CLCNKB deletions

21. Diverse molecular causes of unsolved autosomal dominant tubulointerstitial kidney diseases

25. An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypes

38. Clinical Characteristics and Courses of Patients With Autosomal Recessive Polycystic Kidney Disease-Mimicking Phenocopies

40. Germline C1GALT1C1 mutation causes a multisystem chaperonopathy

42. Clinical Characteristics and Courses of Patients With Autosomal Recessive Polycystic Kidney Disease-Mimicking Phenocopies

43. A Low-Cost Sequencing Platform for Rapid Genotyping in ADPKD and its Impact on Clinical Care

45. MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cells

46. Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin-a single-center analysis

47. Germline C1GALT1C1 Mutation Causes a Multisystemic Chaperonopathy with Global Deficiency of Core 1-derived O-Glycosylation

48. Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin—a single-center analysis

49. MAGED2 controls vasopressin-induced aquaporin-2 expression in collecting duct cells

50. Polyhydramnios, Transient Antenatal Bartterʼs Syndrome, and MAGED2 Mutations

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