- Type 1 primary hyperoxaluria in a male infant
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Waddell B, McKenney D
- KMID: 2405115
- Kidney Res Clin Pract.
- 2017 Dec;36(4):393-393.
- doi: 10.23876/j.krcp.2017.36.4.393
No abstract available. -
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- End-stage Renal Disease Caused by Primary Hyperoxaluria
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Lee HK, Kwon OK, Na KR, Suh KS, Kim SZ, Lee KW, Shin YT
- KMID: 2254205
- Korean J Nephrol.
- 2005 Nov;24(6):981-985.
Primary hyperoxaluria is a rare autosomal recessive inherited metabolic disease which results from endogenous overproduction of oxalic acid. It causes variant phenotypes from renal failure in infancy to mere urolithiasis... -
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- A Case of Primary Hyperoxaluria with Renal Allograft Dysfunction
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Song EJ, Cho JH, Yoon YD, Park JY, Choi JY, Yoon SH, Kim YS, Kim CD, Kim YL, Park SH
- KMID: 2142012
- Korean J Nephrol.
- 2011 Nov;30(6):676-681.
Primary hyperoxaluria is a rare disorder of glyoxylate metabolism in which hepatic enzyme deficiencies result in overproduction of oxalate. The resulting elevation of urinary oxalate excretion leads to recurrent urolithiasis... -
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- A rare case of hyperoxaluria presenting with acute liver injury and stone-free kidney injury
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Kim SE, Kim SJ, Chu ST, Yang SH, Kim YS, Cha RH
- KMID: 2381527
- Kidney Res Clin Pract.
- 2015 Jun;34(2):113-116.
- doi: 10.1016/j.krcp.2014.09.006
A 49-year-old woman visited the clinic because of acute hepatitis and acute kidney injury with decreased urine output presenting microscopic hematuria and proteinuria. An abdominal computed tomography revealed a localized,... -
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- A case of kidney transplantation in primary oxalosis
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Kim SJ, Min SK, Jung HI, Chon Y
- KMID: 2324073
- J Korean Soc Transplant.
- 1993 Nov;7(1):237-243.
No abstract available. -
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- Primary Hyperoxaluria in Korean Pediatric Patients
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Choe Y, Lee JM, Kim JH, Cho MH, Kim SH, Lee JH, Park YS, Kang HG, Ha IS, Cheong HI
- KMID: 2464929
- Child Kidney Dis.
- 2019 Oct;23(2):59-66.
- doi: 10.3339/jkspn.2019.23.2.59
BACKGROUND: Primary hyperoxaluria (PH), a rare inborn error of glyoxylate meta bolism causing overproduction of oxalate, is classified into three genetic subgroups: type 1–3 (PH1–PH3) caused by AGXT, GRHPR ,... -
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- Pediatric Liver Transplantation for Metabolic Liver Disease
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Lee S, Campbell D
- KMID: 2324309
- J Korean Soc Transplant.
- 2002 Jun;16(1):126-132.
PURPOSE: Metabolic liver disease may progress to liver cirrhosis or fulminant hepatic failure. Liver transplantation has been indicated in children with metabolic liver disease as an established curative treatment modality. METHODS:... -
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