Found: 7
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Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis.
- Published in:
- Kidney International, 2009, v. 76, n. 12, p. 1268, doi. 10.1038/ki.2009.381
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- Publication type:
- Article
Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 9, p. 1192, doi. 10.1038/ejhg.2014.252
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- Publication type:
- Article
Complement Genetic Variants and FH Desialylation in S. pneumoniae -Haemolytic Uraemic Syndrome.
- Published in:
- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2021.641656
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- Publication type:
- Article
CD44-negative parietal–epithelial cell staining in minimal change disease: association with clinical features, response to corticosteroids and kidney outcome.
- Published in:
- Clinical Kidney Journal, 2022, v. 15, n. 3, p. 545, doi. 10.1093/ckj/sfab215
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- Publication type:
- Article
Hypertension and segmental renal infarction in children: apropos of two cases.
- Published in:
- 2008
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- Publication type:
- Report
Overcoming limits: First ABO incompatible living donor paired kidney transplant in an hypersensitized pediatric recipient in Spain.
- Published in:
- Pediatric Transplantation, 2022, v. 26, n. 8, p. 1, doi. 10.1111/petr.14359
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- Publication type:
- Article
Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome.
- Published in:
- PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0173581
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- Publication type:
- Article