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Clinical Nephrology|January 5, 2002
Cystinuria phenotyping by oral lysine and arginine loadingL de Sanctis, G Bonetti, M Bruno, et al.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|June 20, 2006
Posttransplant recurrence of proteinuria in a case of focal segmental glomerulosclerosis associated with WT1 mutationG M Ghiggeri, F Aucella, G Caridi, et al.Nucleic Acids Research|October 25, 1995
Stability and functional effectiveness of phosphorothioate modified duplex DNA and synthetic 'mini-genes'S A Ciafrè, M Rinaldi, P Gasparini, et al.Human Genetics|April 1, 1995
Analysis of the complete coding region of the CFTR gene in a cohort of CF patients from north-eastern Italy: identification of 90% of the mutationsA Bonizzato, L Bisceglia, C Marigo, et al.American Journal of Human Genetics|October 1, 1995
Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneityP Gasparini, M J Calonge, L Bisceglia, et al.Genomics|October 15, 1996
Genomic structure and organization of the human rBAT gene (SLC3A1)J Purroy, L Bisceglia, M J Calonge, et al.Proceedings of the National Academy of Sciences of the United States of America|October 10, 1995
Genetic heterogeneity in cystinuria: the SLC3A1 gene is linked to type I but not to type III cystinuriaM J Calonge, V Volpini, L Bisceglia, et al.Journal of Medical Genetics|January 7, 2005
New insights into cystinuria: 40 new mutations, genotype-phenotype correlation, and digenic inheritance causing partial phenotypeM Font-Llitjós, M Jiménez-Vidal, L Bisceglia, et al.Contributions to Nephrology|May 15, 2007
Searching for IgA nephropathy candidate genes: genetic studies combined with high throughput innovative investigationsF P Schena, G Cerullo, D D Torres, et al.Kidney International|March 22, 2001
Cystinuria type I: identification of eight new mutations in SLC3A1L Bisceglia, J Purroy, M Jiménez-Vidal, et al.Pageof 10