New Therapeutic Option for Autosomal Dominant Polycystic Kidney Disease Patients With Enlarged Kidney and Liver-Reference-Cited by-同舟云学术

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New Therapeutic Option for Autosomal Dominant Polycystic Kidney Disease Patients With Enlarged Kidney and Liver

Published:2006-08 Issue:4 Volume:10 Page:333-341
ISSN:1744-9979
Container-title:Therapeutic Apheresis and Dialysis
language:en
Short-container-title:Therapher Dial

Author:

Ubara Yoshifumi

Publisher

Wiley

Subject

Nephrology,Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1744-9987.2006.00386.x/fullpdf

Reference35 articles.

1. The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains

2. The Molecular Basis of Focal Cyst Formation in Human Autosomal Dominant Polycystic Kidney Disease Type I

3. PKD2 , a Gene for Polycystic Kidney Disease That Encodes an Integral Membrane Protein

4. The etiology, pathogenesis, and treatment of autosomal dominant polycystic kidney disease: Recent advances

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1. Incidental renal cell carcinoma post bilateral nephrectomy in autosomal dominant polycystic kidney disease;World Journal of Clinical Cases;2024-10-06

2. Renal cell carcinoma preceded by a rheumatoid‑like paraneoplastic syndrome: A case report;Oncology Letters;2024-07-22

3. A Case of Autosomal Dominant Polycystic Kidney Disease With Resolution of Massive Pericardial Effusion After Renal Transcatheter Artery Embolization;American Journal of Kidney Diseases;2024-02

4. Successful Case of Deceased Donor Liver Transplant for Polycystic Liver Disease;Transplantation Proceedings;2022-12

5. The Safety and Efficacy of Hepatic Transarterial Embolization Using Microspheres and Microcoils in Patients with Symptomatic Polycystic Liver Disease;Journal of Personalized Medicine;2022-10-01

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