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1. Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP)

7. Public support for patients with intractable diseases in Japan: impact on clinical indicators from nationwide registries in patients with autosomal dominant polycystic kidney disease

8. Cover Image

10. Correction to: Public support for patients with intractable diseases in Japan: impact on clinical indicators from nationwide registries in patients with autosomal dominant polycystic kidney disease

15. The Protective Role of KANK1 in Podocyte Injury

19. A case of shock during adsorption ulcer therapy for severe lower chronic limb-threatening ischemia

24. High-flow arteriovenous fistula in X-linked Alport syndrome: a case report

25. Nephrotic syndrome with acute kidney injury due to combination therapy of immune checkpoint inhibitors: A case report and review of the literature

27. A case of carcinoid syndrome probably exacerbated by hemodialysis in which prochlorperazine maleate was effective

28. Bullous Pemphigoid in X-linked Alport Syndrome

34. Cystic Kidney Diseases That Require a Differential Diagnosis from Autosomal Dominant Polycystic Kidney Disease (ADPKD)

35. Mutation Analysis of Thin Basement Membrane Nephropathy

41. A Microbiome-Derived Peptide Induces Apoptosis of Cells from Different Tissues

43. Prognosis of acute myocardial infarction in patients on hemodialysis stratified by Killip classification in the modern interventional era (focus on the prognosis of Killip class 1)

47. Collagenofibrotic Glomerulopathy

49. Glcci1 Deficiency Leads to Proteinuria

50. A Kidney Transplant Recipient with Recurrent Henoch-Schönlein Purpura Nephritis Successfully Treated with Steroid Pulse Therapy and Epipharyngeal Abrasive Therapy

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