Quantification of plasma BK polyomavirus loads is affected by sequence variability, amplicon length, and non-encapsidated viral DNA genome fragments-Reference-Cited by-同舟云学术

Quantification of plasma BK polyomavirus loads is affected by sequence variability, amplicon length, and non-encapsidated viral DNA genome fragments

Published:2019-12 Issue: Volume:121 Page:104210
ISSN:1386-6532
Container-title:Journal of Clinical Virology
language:en
Short-container-title:Journal of Clinical Virology

Author:

Leuzinger Karoline,Naegele Klaudia,Schaub Stefan,Hirsch Hans H.

Funder

Clinical Virology Division, Laboratory Medicine, University Hospital Basel, Basel, Switzerland

Publisher

Elsevier BV

Subject

Infectious Diseases,Virology

Reference29 articles.

1. BK virus: opportunity makes a pathogen;Hirsch;Clin. Infect. Dis.,2005

2. JE Greenlee, HH Hirsch. Polyomaviruses Microbiology AASf, Clinical Virology, 4th Edition. 4th Edition ed. asmscience.org 2017. 599–623.

3. Human polyomavirus and papillomavirus infection and disease posttransplant;Hirsch,2016

4. ECIL guidelines for the prevention, diagnosis and treatment of BK polyomavirus-associated haemorrhagic cystitis in haematopoietic stem cell transplant recipients;Cesaro;J. Antimicrob. Chemother.,2018

5. BK polyomavirus in solid organ transplantation-guidelines from the American Society of Transplantation Infectious Diseases Community of Practice;Hirsch;Clin. Transplant.,2019

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