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Journal of Nephrology|May 30, 1998
Molecular analysis of the AGXT gene in Italian patients with primary hyperoxaluria type 1 (PH1)C Ferrettini, D Pirulli, D Cosseddu, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Detection of primary hyperoxaluria type 2 (L-glyceric aciduria) in patients with maintained renal function or end-stage renal failureM Marangella, M Petrarulo, D Cosseddu, et al.Clinical Science (London, England : 1979)|October 24, 1997
Different dietary calcium intake and relative supersaturation of calcium oxalate in the urine of patients forming renal stonesP Messa, M Marangella, L Paganin, et al.Human Genetics|August 24, 1999
Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase geneD Pirulli, D Puzzer, L Ferri, et al.Kidney International|July 1, 1995
Bony content of oxalate in patients with primary hyperoxaluria or oxalosis-unrelated renal failureM Marangella, C Vitale, M Petrarulo, et al.American Journal of Nephrology|January 1, 1990
Primary oxalosis mimicking hyperparathyroidism diagnosed after long-term hemodialysisC Canavese, M Salomone, C Massara, et al.Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 9, 2002
[Intact whole bioactive parathormone: problems arising from comparing different methods]M Marangella, M Migliardi, F Dutto, et al.Nephron|January 1, 1993
Long-term survival on renal replacement therapy for primary hyperoxaluria type IP Calzavara, M Marangella, M Petrarulo, et al.Pageof 67