Clinical Features and Outcome in Children With Primary Hyperoxaluria; Single Center Experience
Journal of Pediatric Nephrology,
Vol. 3 No. 3 (2015),
6 July 2015
,
Page 121-123
https://doi.org/10.22037/jpn.v3i3.8860
Abstract
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References
Cochat P, Rumsby G. Primary Hyperoxaluria. N Engl J Med 2013;369(7):649-658.
Leal R, Santos T, Galvão A, Macário F, Pratas J, Cunha FX, Vilarinho L, Campos M. Primary hyperoxaluria type 1: A literature review upon three clinical cases. Port J Nephrol Hypert 2014;28(4):281-289.
Mandrile G, van Woerden CS, Berchialla P, Beck BB, Acquaviva Bourdain C, Hulton SA, Rumsby G; OxalEurope Consortium. Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation type. Kidney Int. 2014;86(6):1197-204.
Hoyer-Kuhn H, Kohbrok S, Volland R, Franklin J, Hero B, Beck BB, Hoppe B. Vitamin B6 in primary hyperoxaluria I: first prospective trial after 40 years of practice. Clin J Am Soc Nephrol. 2014;9(3):468-77.
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