Examination of the eye and retinal alterations in primary hyperoxaluria type 1

Author:

Birtel Johannes1234ORCID,Charbel Issa Peter34,Herrmann Philipp12,Hoppe Bernd256,Büscher Anja Katrin7

Affiliation:

1. Department of Ophthalmology, University of Bonn, Bonn, Germany

2. Center for Rare Diseases Bonn (ZSEB), University of Bonn, Bonn, Germany

3. Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK

4. Nuffield Laboratory of Ophthalmology, Department of Clinical Neurosciences, University of Oxford, Oxford, UK

5. OxalEurope, The European Hyperoxaluria Consortium, Cologne, Germany

6. Department of Pediatrics, Division of Pediatric Nephrology, University of Bonn, Bonn, Germany

7. Department of Pediatric Nephrology, University Children's Hospital Essen, Essen, Germany

Funder

Dr. Werner Jackstädt Foundation, Wuppertal, Germany

National Institute for Health Research (NIHR) Oxford Biomedical Research Centre

German Research Foundation

National Health Service

NIHR

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. The retinal phenotype in primary hyperoxaluria type 2 and 3;Pediatric Nephrology;2022-10-19

2. Hyperoxaluria;Pediatric Nephrology;2022

3. North Carolina macular dystrophy shows a particular drusen phenotype and atrophy progression;British Journal of Ophthalmology;2021-03-30

4. Diagnosis of Inherited Retinal Diseases;Klinische Monatsblätter für Augenheilkunde;2021-03

5. Hyperoxaluria;Pediatric Nephrology;2021

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