about
Nephrolithiasis related to inborn metabolic diseasesDisease recurrence in paediatric renal transplantationProline dehydrogenase 2 (PRODH2) is a hydroxyproline dehydrogenase (HYPDH) and molecular target for treating primary hyperoxaluriaUnusual clinical outcome of primary Hyperoxaluria type 1 in Tunisian patients carrying 33_34InsC mutation.Hereditary causes of kidney stones and chronic kidney diseaseKidney stones in primary hyperoxaluria: new lessons learnt.Primary hyperoxaluria.Primary and secondary hyperoxaluria: Understanding the enigmaCharacteristics and outcomes of children with primary oxalosis requiring renal replacement therapySurgical management of stone disease in patients with primary hyperoxaluria.Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria.Acute oxalate nephropathy following kidney transplantation: Report of three cases.Inhibition of Glycolate Oxidase With Dicer-substrate siRNA Reduces Calcium Oxalate Deposition in a Mouse Model of Primary Hyperoxaluria Type 1.An update on primary hyperoxaluria.Hyperoxaluria and systemic oxalosis: an update on current therapy and future directions.Extracorporal shock wave lithotripsy in the management of stones in children with oxalosis--still the first choice?Primary hyperoxaluria type 1: practical and ethical issues.Helper-dependent adenoviral vectors for liver-directed gene therapy of primary hyperoxaluria type 1.Bone impairment in primary hyperoxaluria: a review.Primary hyperoxaluria type 1 in 18 children: genotyping and outcome.Review of combined liver and kidney transplantation in children.Successful long-term outcome of pediatric liver-kidney transplantation: a single-center study.Liver involvement in kidney disease and vice versa.Hyperoxaluria and rapid development of renal failure following a combined liver and kidney transplantation: emphasis on sequential transplantation.Primary hyperoxaluria type 1, a too often missed diagnosis and potentially treatable cause of end-stage renal disease in adults: results of the Dutch cohort.Liver transplantation for primary hyperoxaluria type 1: a single-center experience during two decades in Japan.Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center.Pathological features of oxalate nephrosis in a population of koalas (Phascolarctos cinereus) in South Australia.HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tunisian Patients.Bilateral native nephrectomy to reduce oxalate stores in children at the time of combined liver-kidney transplantation for primary hyperoxaluria type 1.An institutional experience of pre-emptive liver transplantation for pediatric primary hyperoxaluria type 1.Complexity of pre-emptive liver transplantation in children with primary hyperoxaluria type 1.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Primary hyperoxaluria type 1: still challenging!
@ast
Primary hyperoxaluria type 1: still challenging!
@en
type
label
Primary hyperoxaluria type 1: still challenging!
@ast
Primary hyperoxaluria type 1: still challenging!
@en
prefLabel
Primary hyperoxaluria type 1: still challenging!
@ast
Primary hyperoxaluria type 1: still challenging!
@en
P2093
P1433
P1476
Primary hyperoxaluria type 1: still challenging!
@en
P2093
Aurélia Liutkus
Bruno Ranchin
Marie-Odile Rolland
Odile Basmaison
Pierre Cochat
P2888
P304
P356
10.1007/S00467-006-0124-4
P50
P577
2006-06-30T00:00:00Z