Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1
Authors
Keywords
-
Journal
Clinical Journal of the American Society of Nephrology
Volume -, Issue -, Pages CJN.14730920
Publisher
American Society of Nephrology (ASN)
Online
2021-05-13
DOI
10.2215/cjn.14730920
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Endpoints for Clinical Trials in Primary Hyperoxaluria
- (2020) Dawn S. Milliner et al. Clinical Journal of the American Society of Nephrology
- Characterising a healthy adult with a rare HAO1 knockout to support a therapeutic strategy for primary hyperoxaluria
- (2020) Tracy L McGregor et al. eLife
- GalNAc-siRNA Conjugates: Leading the Way for Delivery of RNAi Therapeutics
- (2018) Aaron D. Springer et al. Nucleic Acid Therapeutics
- Glycolate oxidase deficiency in a patient with congenital hyperinsulinism and unexplained hyperoxaluria
- (2017) Oliver Clifford-Mobley et al. PEDIATRIC NEPHROLOGY
- An Investigational RNAi Therapeutic Targeting Glycolate Oxidase Reduces Oxalate Production in Models of Primary Hyperoxaluria
- (2016) Abigail Liebow et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Inhibition of Glycolate Oxidase With Dicer-substrate siRNA Reduces Calcium Oxalate Deposition in a Mouse Model of Primary Hyperoxaluria Type 1
- (2016) Chaitali Dutta et al. MOLECULAR THERAPY
- An institutional experience of pre-emptive liver transplantation for pediatric primary hyperoxaluria type 1
- (2016) Shirin Elizabeth Khorsandi et al. PEDIATRIC TRANSPLANTATION
- Predictors of Incident ESRD among Patients with Primary Hyperoxaluria Presenting Prior to Kidney Failure
- (2015) F. Zhao et al. Clinical Journal of the American Society of Nephrology
- Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria
- (2015) K. Hopp et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Mutations inHAO1encoding glycolate oxidase cause isolated glycolic aciduria
- (2014) Yaacov Frishberg et al. JOURNAL OF MEDICAL GENETICS
- Primary Hyperoxaluria
- (2013) Pierre Cochat et al. NEW ENGLAND JOURNAL OF MEDICINE
- An update on primary hyperoxaluria
- (2012) Bernd Hoppe Nature Reviews Nephrology
- Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment
- (2012) P. Cochat et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1
- (2009) Sonia Fargue et al. KIDNEY INTERNATIONAL
- Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome
- (2009) Jérôme Harambat et al. KIDNEY INTERNATIONAL
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started