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Clinical and Experimental Immunology|July 28, 2005
Circulating anti-actin and anti-ATP synthase antibodies identify a sub-set of patients with idiopathic nephrotic syndromeL Musante, G Candiano, M Bruschi, et al.
American Journal of Human Genetics|May 1, 1989
Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and SwitzerlandS E Sullivan, S D Moore, J M Connor, et al.
The New England Journal of Medicine|April 2, 1992
Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative StudyP Tsipouras, R Del Mastro, M Sarfarazi, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|April 4, 1998
The Italian Registry of Pediatric Chronic Peritoneal Dialysis: a ten-year experience with chronic peritoneal dialysis cathetersS Rinaldi, F Sera, E Verrina, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|January 1, 1996
Comparison of patient hospitalization in chronic peritoneal dialysis and hemodialysis: a pediatric multicenter studyE Verrina, F Perfumo, G Zacchello, et al.
Cell|December 31, 1993
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidismM R Pollak, E M Brown, Y H Chou, et al.
American Journal of Human Genetics|September 1, 1991
Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the geneK Kainulainen, B Steinmann, F Collins, et al.
American Journal of Human Genetics|June 1, 1996
Mutations and phenotype in isolated glycerol kinase deficiencyA P Walker, F Muscatelli, A N Stafford, et al.
Pediatric Nephrology (Berlin, Germany)|February 24, 2001
Successful renal transplantation in children under 6 years of ageR Dall'Amico, F Ginevri, L Ghio, et al.
Genomics|September 24, 1999
Recombinant families locate the gene for non-type I cystinuria between markers C13 and D19S587 on chromosome 19q13.1L Feliubadaló, L Bisceglia, M Font, et al.
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