150 related articles for article (PubMed ID: 37954792)
1. A Rare Sparkle: A Case of Calcified Kidneys in a Young Infant With Renal Failure.
Mittal A; Jain H; Singh A; Yadav T; Vishwajeet V
Cureus; 2023 Oct; 15(10):e46827. PubMed ID: 37954792
[TBL] [Abstract][Full Text] [Related]
2. Combined liver-kidney transplantation for primary hyperoxaluria type 1 in young children.
Ellis SR; Hulton SA; McKiernan PJ; de Ville de Goyet J; Kelly DA
Nephrol Dial Transplant; 2001 Feb; 16(2):348-54. PubMed ID: 11158411
[TBL] [Abstract][Full Text] [Related]
3. Liver-kidney transplantation in primary hyperoxaluria type-1: case report and literature review.
Siegal D; Su WS; DaBreo D; Puglia M; Gregor L; Gangji AS
Int J Organ Transplant Med; 2011; 2(3):126-32. PubMed ID: 25013605
[TBL] [Abstract][Full Text] [Related]
4. Generation and characterization of a novel rat model of primary hyperoxaluria type 1 with a nonsense mutation in alanine-glyoxylate aminotransferase gene.
Li Y; Zheng R; Xu G; Huang Y; Li Y; Li D; Geng H
Am J Physiol Renal Physiol; 2021 Mar; 320(3):F475-F484. PubMed ID: 33491567
[TBL] [Abstract][Full Text] [Related]
5. Recurrence of crystalline nephropathy after kidney transplantation in APRT deficiency and primary hyperoxaluria.
Bollée G; Cochat P; Daudon M
Can J Kidney Health Dis; 2015; 2():31. PubMed ID: 26380104
[TBL] [Abstract][Full Text] [Related]
6. A test of the hypothesis that oxalate secretion produces proximal tubule crystallization in primary hyperoxaluria type I.
Worcester EM; Evan AP; Coe FL; Lingeman JE; Krambeck A; Sommers A; Phillips CL; Milliner D
Am J Physiol Renal Physiol; 2013 Dec; 305(11):F1574-84. PubMed ID: 24089413
[TBL] [Abstract][Full Text] [Related]
7. Primary hyperoxaluria complicated with liver cirrhosis: A case report.
Kogiso T; Tokushige K; Hashimoto E; Miyakata C; Taniai M; Torii N; Omori A; Kotera Y; Egawa H; Yamamoto M; Nagata M; Shiratori K
Hepatol Res; 2015 Dec; 45(12):1251-5. PubMed ID: 25594663
[TBL] [Abstract][Full Text] [Related]
8. Recurrence of primary hyperoxaluria after kidney transplantation.
Malakoutian T; Asgari M; Houshmand M; Mohammadi R; Aryani O; Mohammadi Pargoo E; Ghods AJ
Iran J Kidney Dis; 2011 Nov; 5(6):429-33. PubMed ID: 22057078
[TBL] [Abstract][Full Text] [Related]
9. Extreme intrafamilial variability of Saudi brothers with primary hyperoxaluria type 1.
Alfadhel M; Alhasan KA; Alotaibi M; Al Fakeeh K
Ther Clin Risk Manag; 2012; 8():373-6. PubMed ID: 22956877
[TBL] [Abstract][Full Text] [Related]
10. Nocturnal home hemodialysis for a patient with type 1 hyperoxaluria.
Plumb TJ; Swee ML; Fillaus JA
Am J Kidney Dis; 2013 Dec; 62(6):1155-9. PubMed ID: 23830800
[TBL] [Abstract][Full Text] [Related]
11. Combined liver-kidney transplantation in primary hyperoxaluria type 1.
Cochat P; Gaulier JM; Koch Nogueira PC; Feber J; Jamieson NV; Rolland MO; Divry P; Bozon D; Dubourg L
Eur J Pediatr; 1999 Dec; 158 Suppl 2():S75-80. PubMed ID: 10603104
[TBL] [Abstract][Full Text] [Related]
12. Combined liver-kidney and isolated liver transplantations for primary hyperoxaluria type 1: the European experience. The European Study Group on Transplantation in Hyperoxaluria Type 1.
Watts RW; Danpure CJ; De Pauw L; Toussaint
Nephrol Dial Transplant; 1991; 6(7):502-11. PubMed ID: 1922912
[TBL] [Abstract][Full Text] [Related]
13. Encapsulating peritoneal sclerosis in a patient with primary hyperoxaluria type 1: a case report.
Vanmassenhove J; Vanholder R; Forsyth R; Dhondt A
Perit Dial Int; 2010; 30(1):108-11. PubMed ID: 20056990
[TBL] [Abstract][Full Text] [Related]
14. Systemic Alanine Glyoxylate Aminotransferase mRNA Improves Glyoxylate Metabolism in a Mouse Model of Primary Hyperoxaluria Type 1.
Kukreja A; Lasaro M; Cobaugh C; Forbes C; Tang JP; Gao X; Martin-Higueras C; Pey AL; Salido E; Sobolov S; Subramanian RR
Nucleic Acid Ther; 2019 Apr; 29(2):104-113. PubMed ID: 30676254
[TBL] [Abstract][Full Text] [Related]
15. Early and unusual presentation of type I primary hyperoxaluria.
Giugliani R; Jardim L; Edelweiss MI; Rosa A
Child Nephrol Urol; 1990; 10(2):107-8. PubMed ID: 2253247
[TBL] [Abstract][Full Text] [Related]
16. Identification of a novel AGXT gene mutation in primary hyperoxaluria after kidney transplantation failure.
M'dimegh S; Omezzine A; Hamida-Rebai MB; Aquaviva-Bourdain C; M'barek I; Sahtout W; Zellama D; Souche G; Achour A; Abroug S; Bouslama A
Transpl Immunol; 2016 Nov; 39():60-65. PubMed ID: 27568336
[TBL] [Abstract][Full Text] [Related]
17. Primary hyperoxaluria type 1: pathophysiology and genetics.
Fargue S; Acquaviva Bourdain C
Clin Kidney J; 2022 May; 15(Suppl 1):i4-i8. PubMed ID: 35592619
[TBL] [Abstract][Full Text] [Related]
18. Oxalosis in primary hyperoxaluria in infancy : Report of a case in a 3-month-old baby. Follow-up for 3 years and review of literature.
Orazi C; Picca S; Schingo PM; Fassari FM; Canepa G
Skeletal Radiol; 2009 Apr; 38(4):387-91. PubMed ID: 19132372
[TBL] [Abstract][Full Text] [Related]
19. [Primary hyperoxaluria].
Toussaint C; De Pauw L
Nephrologie; 1995; 16(6):399-406. PubMed ID: 8524446
[TBL] [Abstract][Full Text] [Related]
20. Primary Hyperoxaluria Type 1: A Cause for Infantile Renal Failure and Massive Nephrocalcinosis.
Kurt-Sukur ED; Özçakar ZB; Fitöz S; Yilmaz S; Hoppe B; Yalçinkaya F
Klin Padiatr; 2015 Sep; 227(5):293-5. PubMed ID: 26090995
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]