Found: 7
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Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome.
- Published in:
- Kidney International, 2010, v. 77, n. 5, p. 443, doi. 10.1038/ki.2009.435
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- Article
Both extrauterine and intrauterine growth restriction impair renal function in children born very preterm.
- Published in:
- Kidney International, 2009, v. 76, n. 4, p. 445, doi. 10.1038/ki.2009.201
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- Article
Nephrolithiasis related to inborn metabolic diseases.
- Published in:
- Pediatric Nephrology, 2010, v. 25, n. 3, p. 415, doi. 10.1007/s00467-008-1085-6
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- Article
HHV-6 infection in a pediatric kidney transplant patient.
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- Pediatric Nephrology, 2009, v. 24, n. 12, p. 2445, doi. 10.1007/s00467-009-1237-3
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- Article
Primary hyperoxaluria type 1: still challenging!
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- Pediatric Nephrology, 2006, v. 21, n. 8, p. 1075, doi. 10.1007/s00467-006-0124-4
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- Article
NPHS2 Mutations in Steroid-Resistant Nephrotic Syndrome: A Mutation Update and the Associated Phenotypic Spectrum.
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- Human Mutation, 2014, v. 35, n. 2, p. 178, doi. 10.1002/humu.22485
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- Article
Pseudohypoaldosteronisms, report on a 10-patient series.
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- Nephrology Dialysis Transplantation, 2008, v. 23, n. 5, p. 1636, doi. 10.1093/ndt/gfm862
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- Article