Found: 16
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WT1 gene mutations in three girls with nephrotic syndrome.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Hereditary polycystic kidney diseases in children: changing sonographic patterns through childhood.
- Published in:
- 2002
- By:
- Publication type:
- journal article
CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency.
- Published in:
- Journal of Clinical Investigation, 2010, v. 120, n. 4, p. 1265, doi. 10.1172/JCI39748
- By:
- Publication type:
- Article
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
- By:
- Publication type:
- Article
Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1.
- Published in:
- Kidney International, 2009, v. 76, n. 7, p. 767, doi. 10.1038/ki.2009.237
- By:
- Publication type:
- Article
Transverse comparisons between ultrasound and radionuclide parameters in children with presumed antenatally detected pelvi-ureteric junction obstruction.
- Published in:
- European Journal of Nuclear Medicine & Molecular Imaging, 2015, v. 42, n. 6, p. 940, doi. 10.1007/s00259-014-2965-6
- By:
- Publication type:
- Article
Epidemiological urinalysis of children from kindergartens of Can Gio, Ho Chi Minh City - Vietnam.
- Published in:
- BMC Pediatrics, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2431-13-183
- By:
- Publication type:
- Article
Epidemiological urinalysis of children from kindergartens of Can Gio, Ho Chi Minh City - Vietnam.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Clinical characteristics and outcomes of children with stage 3–5 chronic kidney disease.
- Published in:
- Pediatric Nephrology, 2010, v. 25, n. 5, p. 935, doi. 10.1007/s00467-009-1424-2
- By:
- Publication type:
- Article
Genetic forms of nephrotic syndrome: a single-center experience in Brussels.
- Published in:
- Pediatric Nephrology, 2009, v. 24, n. 2, p. 287, doi. 10.1007/s00467-008-0953-4
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- Publication type:
- Article
Genetic forms of nephrotic syndrome: a single-center experience in Brussels.
- Published in:
- 2009
- By:
- Publication type:
- Correction Notice
Etiology and outcome of chronic renal failure in hospitalized children in Ho Chi Minh City, Vietnam.
- Published in:
- Pediatric Nephrology, 2008, v. 23, n. 6, p. 965, doi. 10.1007/s00467-008-0752-y
- By:
- Publication type:
- Article
Neonatal disease in neutral endopeptidase alloimmunization: lessons for immunological monitoring.
- Published in:
- Pediatric Nephrology, 2006, v. 21, n. 10, p. 1399, doi. 10.1007/s00467-006-0203-6
- By:
- Publication type:
- Article
Early prognostic factors of infants with chronic renal failure caused by renal dysplasia.
- Published in:
- Pediatric Nephrology, 2001, v. 16, n. 3, p. 260, doi. 10.1007/s004670000539
- By:
- Publication type:
- Article
Mutations in the human laminin β2 ( LAMB2) gene and the associated phenotypic spectrum.
- Published in:
- 2010
- By:
- Publication type:
- Other
Evaluation of clinical and biological parameters in marastic Kwashiorkor children treated by parenteral nutrition.
- Published in:
- 1983
- By:
- Publication type:
- journal article