Found: 16
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PAX3 Is Expressed in the Stromal Compartment of the Developing Kidney and in Wilms Tumors with Myogenic Phenotype.
- Published in:
- Pediatric & Developmental Pathology, 2009, v. 12, n. 5, p. 347, doi. 10.2350/08-05-0466.1
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- Publication type:
- Article
T-cell factor/β-catenin activity is suppressed in two different models of autosomal dominant polycystic kidney disease.
- Published in:
- 2011
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- Publication type:
- journal article
T-cell factor/β-catenin activity is suppressed in two different models of autosomal dominant polycystic kidney disease.
- Published in:
- Kidney International, 2011, v. 80, n. 2, p. 146, doi. 10.1038/ki.2011.56
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- Publication type:
- Article
Renal Chloride Channel, CLCN5, Mutations in Dent's Disease.
- Published in:
- Journal of Bone & Mineral Research, 1999, v. 14, n. 9, p. 1536, doi. 10.1359/jbmr.1999.14.9.1536
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- Publication type:
- Article
Reduction of protein excretion by dimethyl sulfoxide in rats with passive Heymann nephritis.
- Published in:
- Kidney International, 1984, v. 25, n. 5, p. 778, doi. 10.1038/ki.1984.90
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- Publication type:
- Article
Transition From Pediatric to Adult Nephrology Care: Program Report of a Single-Center Experience.
- Published in:
- Canadian Journal of Kidney Health & Disease, 2023, p. 1, doi. 10.1177/20543581231191836
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- Publication type:
- Article
Transition From Pediatric to Adult Nephrology Care: Program Report of a Single-Center Experience.
- Published in:
- Canadian Journal of Kidney Health & Disease, 2023, v. 10, p. 1, doi. 10.1177/20543581231191836
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- Publication type:
- Article
A no-nonsense approach to hereditary kidney disease.
- Published in:
- Pediatric Nephrology, 2020, v. 35, n. 11, p. 2031, doi. 10.1007/s00467-019-04394-5
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- Publication type:
- Article
Use of genomic and functional analysis to characterize patients with steroid-resistant nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2018, v. 33, n. 10, p. 1741, doi. 10.1007/s00467-018-3995-2
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- Publication type:
- Article
Clinical features of X-linked nephrolithiasis in childhood.
- Published in:
- Pediatric Nephrology, 1998, v. 12, n. 8, p. 625, doi. 10.1007/s004670050516
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- Publication type:
- Article
Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1543, doi. 10.1093/hmg/ddp050
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- Publication type:
- Article
Pax2 gene dosage influences cystogenesis in autosomal dominant polycystic kidney disease.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 24, p. 3520, doi. 10.1093/hmg/ddl428
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- Publication type:
- Article
Turner's syndrome, 46X, del (X) (p 11), persistent complement activation and membranoproliferative glomerulonephritis.
- Published in:
- 1982
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- Publication type:
- journal article
CLCN5 chloride-channel mutations in six new North American families with X-linked nephrolithiasis.
- Published in:
- Kidney International, 1998, v. 54, n. 3, p. 698, doi. 10.1046/j.1523-1755.1998.00061.x
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- Publication type:
- Article
Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain.
- Published in:
- Kidney International, 1998, v. 54, n. 3, p. 720, doi. 10.1046/j.1523-1755.1998.00070.x
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- Publication type:
- Article
Molecular genetics of cystinuria in French Canadians: identification of four novel mutations in type I patients.
- Published in:
- 1996
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- Publication type:
- journal article