about
A novel mutation in the GRHPR gene in a Japanese patient with primary hyperoxaluria type 2The comparability of oxalate excretion and oxalate:creatinine ratio in the investigation of primary hyperoxaluria: review of data from a referral centre.Hereditary causes of kidney stones and chronic kidney diseaseTransplantation outcomes in primary hyperoxaluria.Performance evaluation of Sanger sequencing for the diagnosis of primary hyperoxaluria and comparison with targeted next generation sequencingPrimary and secondary hyperoxaluria: Understanding the enigmaA rare case of hyperoxaluria presenting with acute liver injury and stone-free kidney injury.Hyperoxaluria and systemic oxalosis: current therapy and future directions.Genetic determinants of urolithiasis.Cardiac abnormalities in primary hyperoxaluria.An update on primary hyperoxaluria.Primary hyperoxalurias: diagnosis and treatment.An expanded syndrome of dRTA with hearing loss, hyperoxaluria and beta2-microglobulinuria.Autopsy findings of a case with oxalosis.Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center.The urinary metabolomics profile of an Italian autistic children population and their unaffected siblings.Genetic Causes of Kidney Stones and Kidney Failure
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
2005年论文
@zh
2005年论文
@zh-cn
name
The primary hyperoxalurias: an algorithm for diagnosis.
@ast
The primary hyperoxalurias: an algorithm for diagnosis.
@en
type
label
The primary hyperoxalurias: an algorithm for diagnosis.
@ast
The primary hyperoxalurias: an algorithm for diagnosis.
@en
prefLabel
The primary hyperoxalurias: an algorithm for diagnosis.
@ast
The primary hyperoxalurias: an algorithm for diagnosis.
@en
P2860
P356
P1476
The primary hyperoxalurias: an algorithm for diagnosis.
@en
P2093
Dawn S Milliner
P2860
P304
P356
10.1159/000085407
P577
2005-03-01T00:00:00Z