标题
The retinal phenotype in primary hyperoxaluria type 2 and 3
作者
关键词
-
出版物
PEDIATRIC NEPHROLOGY
Volume -, Issue -, Pages -
出版商
Springer Science and Business Media LLC
发表日期
2022-10-19
DOI
10.1007/s00467-022-05765-1
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- A report from the European Hyperoxaluria Consortium (OxalEurope) Registry on a large cohort of patients with primary hyperoxaluria type 3
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- Diagnosis of Inherited Retinal Diseases
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- Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1
- (2021) Sander F. Garrelfs et al. NEW ENGLAND JOURNAL OF MEDICINE
- Primary Hyperoxaluria Type 3 Can Also Result in Kidney Failure: A Case Report
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- Oxalobacter formigenes treatment combined with intensive dialysis lowers plasma oxalate and halts disease progression in a patient with severe infantile oxalosis
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- Comprehensive Geno- and Phenotyping in a Complex Pedigree Including Four Different Inherited Retinal Dystrophies
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- (2019) Yevgeniya Atiskova et al. AMERICAN JOURNAL OF TRANSPLANTATION
- Patients with primary hyperoxaluria type 2 have significant morbidity and require careful follow-up
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- Bildgebung und molekulargenetische Diagnostik zur Charakterisierung von Netzhautdystrophien
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- Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation
- (2017) Jennifer E. Posey et al. NEW ENGLAND JOURNAL OF MEDICINE
- DETAILED CLINICAL PHENOTYPING OF OXALATE MACULOPATHY IN PRIMARY HYPEROXALURIA TYPE 1 AND REVIEW OF THE LITERATURE
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- A New Equation to Estimate Glomerular Filtration Rate
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- Primary Hyperoxaluria
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- An update on primary hyperoxaluria
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- Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies
- (2009) S Bernal et al. CLINICAL GENETICS
- New Equations to Estimate GFR in Children with CKD
- (2009) G. J. Schwartz et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
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