Combined liver-kidney and kidney-alone transplantation in primary hyperoxaluria

scientific article published in November 2001

Combined liver-kidney and kidney-alone transplantation in primary hyperoxaluria is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1053/JLTS.2001.28741
P698PubMed publication ID11699031
P5875ResearchGate publication ID11655532

P2093author name stringMilliner DS
Monico CG
P2860cites workThe gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patients with primary hyperoxaluria type IIQ22010369
Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type IQ24299643
Combined liver-kidney transplantation for primary hyperoxaluria type 1 in young childrenQ31832605
Kidney transplantation in primary oxalosis: data from the EDTA RegistryQ33771313
Liver transplantation in children: long-term outcome and quality of lifeQ33797818
Identification of missense, nonsense, and deletion mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2).Q33921289
Sensory neuropathy from pyridoxine abuse. A new megavitamin syndromeQ34254765
Evidence that serum calcium oxalate supersaturation is a consequence of oxalate retention in patients with chronic renal failureQ36994464
Primary hyperoxaluria type I.Q37928429
Transplantation for primary hyperoxaluria in the United StatesQ42609011
Phenotypic expression of primary hyperoxaluria: comparative features of types I and II.Q43514404
Combined hepatic and renal transplantation in primary hyperoxaluria type I: clinical report of nine casesQ44520325
Preemptive liver transplantation from a living related donor for primary hyperoxaluria type I.Q55067573
P433issue11
P304page(s)954-963
P577publication date2001-11-01
P1433published inLiver TransplantationQ15730498
P1476titleCombined liver-kidney and kidney-alone transplantation in primary hyperoxaluria
P478volume7

Reverse relations

cites work (P2860)
Q46551815A 20-year experience of combined liver/kidney transplantation for primary hyperoxaluria (PH1): the European PH1 transplant registry experience 1984-2004.
Q38017938An update on primary hyperoxaluria
Q48113340Bilateral native nephrectomy to reduce oxalate stores in children at the time of combined liver-kidney transplantation for primary hyperoxaluria type 1.
Q34261036Canadian Society of Transplantation: consensus guidelines on eligibility for kidney transplantation
Q34719077Enteric oxalate elimination is induced and oxalate is normalized in a mouse model of primary hyperoxaluria following intestinal colonization with Oxalobacter
Q38061207Hyperoxaluria and systemic oxalosis: an update on current therapy and future directions
Q36613873Hyperoxaluria and systemic oxalosis: current therapy and future directions
Q63441488Hyperoxalurie primitive
Q35574335Intra-operative continuous renal replacement therapy during combined liver-kidney transplantation in two patients with primary hyperoxaluria type 1.
Q81893017Liquid chromatography-tandem mass spectrometry method for routine measurement of oxalic acid in human plasma
Q38228334Liver-kidney transplantation in primary hyperoxaluria type-1: case report and literature review
Q35798380Oxalate quantification in hemodialysate to assess dialysis adequacy for primary hyperoxaluria
Q80124022Presentation and role of transplantation in adult patients with type 1 primary hyperoxaluria and the I244T AGXT mutation: Single-center experience
Q83105908Restrictive cardiomyopathy in a patient with primary hyperoxaluria type II
Q35977167Sustained pyridoxine response in primary hyperoxaluria type 1 recipients of kidney alone transplant
Q83370521The primary hyperoxalurias
Q34247162Transplantation Outcomes in Primary Hyperoxaluria
Q38105961Update on oxalate crystal disease

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