Found: 25
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Single‐cell transcriptomics identifies aberrant glomerular angiogenic signalling in the early stages of WT1 kidney disease.
- Published in:
- Journal of Pathology, 2024, v. 264, n. 2, p. 212, doi. 10.1002/path.6339
- By:
- Publication type:
- Article
Mutations in LAMB2 Are Associated With Albuminuria and Optic Nerve Hypoplasia With Hypopituitarism.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2020, v. 105, n. 3, p. 595, doi. 10.1210/clinem/dgz216
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- Publication type:
- Article
Mutations in LAMB2 Are Associated With Albuminuria and Optic Nerve Hypoplasia With Hypopituitarism.
- Published in:
- 2019
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- Publication type:
- journal article
Childhood hemolytic uremic syndrome, United Kingdom and Ireland.
- Published in:
- 2005
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- Publication type:
- journal article
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome.
- Published in:
- Nature Genetics, 2011, v. 43, n. 3, p. 197, doi. 10.1038/ng.757
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- Publication type:
- Article
Characterisation and Validation of Insertions and Deletions in 173 Patient Exomes.
- Published in:
- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0051292
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- Publication type:
- Article
Mendelian steroid resistant nephrotic syndrome in childhood: is it as common as reported?
- Published in:
- Pediatric Nephrology, 2023, v. 38, n. 4, p. 1051, doi. 10.1007/s00467-022-05569-3
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- Publication type:
- Article
Long-term obesity prevalence and linear growth in children with idiopathic nephrotic syndrome: is normal growth and weight control possible with steroid-sparing drugs and low-dose steroids for relapses?
- Published in:
- Pediatric Nephrology, 2022, v. 37, n. 7, p. 1575, doi. 10.1007/s00467-021-05288-1
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- Publication type:
- Article
The effect of levamisole on kidney function in children with steroid-sensitive nephrotic syndrome.
- Published in:
- Pediatric Nephrology, 2021, v. 36, n. 11, p. 3799, doi. 10.1007/s00467-021-05231-4
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- Publication type:
- Article
Early relapse of atypical hemolytic uremic syndrome following ABO-incompatible living–related pediatric kidney re-transplant successfully treated with eculizumab.
- Published in:
- Pediatric Nephrology, 2021, v. 36, n. 10, p. 3271, doi. 10.1007/s00467-021-05193-7
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- Publication type:
- Article
Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations.
- Published in:
- Journal of Inherited Metabolic Disease, 2018, v. 41, n. 5, p. 865, doi. 10.1007/s10545-018-0147-6
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- Publication type:
- Article
Clinico-pathological correlations of congenital and infantile nephrotic syndrome over twenty years.
- Published in:
- Pediatric Nephrology, 2014, v. 29, n. 11, p. 2173, doi. 10.1007/s00467-014-2856-x
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- Publication type:
- Article
Successful treatment of DEAP-HUS with eculizumab.
- Published in:
- Pediatric Nephrology, 2014, v. 29, n. 5, p. 841, doi. 10.1007/s00467-013-2654-x
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- Publication type:
- Article
Erratum to: aHUS caused by complement dysregulation: new therapies on the horizon.
- Published in:
- 2013
- By:
- Publication type:
- Correction Notice
Growth in PHEX-associated X-linked hypophosphatemic rickets: the importance of early treatment.
- Published in:
- Pediatric Nephrology, 2012, v. 27, n. 4, p. 581, doi. 10.1007/s00467-011-2046-z
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- Publication type:
- Article
Optimizing treatment strategies in paediatric atypical hemolytic uremic syndrome.
- Published in:
- 2011
- By:
- Publication type:
- Letter
Ciliopathies: an expanding disease spectrum.
- Published in:
- Pediatric Nephrology, 2011, v. 26, n. 7, p. 1039, doi. 10.1007/s00467-010-1731-7
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- Publication type:
- Article
aHUS caused by complement dysregulation: new therapies on the horizon.
- Published in:
- Pediatric Nephrology, 2011, v. 26, n. 1, p. 41, doi. 10.1007/s00467-010-1556-4
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- Publication type:
- Article
Severe atypical HUS caused by CFH S1191L—case presentation and review of treatment options.
- Published in:
- 2010
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- Publication type:
- Report
Atypical p-ANCA is not a poor prognostic marker in Postinfectious Glomerulonephritis.
- Published in:
- 2007
- By:
- Publication type:
- Report
Malformations in the Murine Kidney Caused by Loss of CENP‐F Function.
- Published in:
- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2019, v. 302, n. 1, p. 163, doi. 10.1002/ar.24018
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- Publication type:
- Article
The CONSENSUS study: protocol for a mixed methods study to establish which outcomes should be included in a core outcome set for oropharyngeal cancer.
- Published in:
- Trials, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1745-6215-15-168
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- Publication type:
- Article
The CONSENSUS study: protocol for a mixed methods study to establish which outcomes should be included in a core outcome set for oropharyngeal cancer.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Efficacy and safety of eculizumab in children with Shiga-toxin-producing Escherichia coli haemolytic uraemic syndrome: the ECUSTEC RCT.
- Published in:
- Efficacy & Mechanism Evaluation (EME), 2024, v. 11, n. 11, p. v, doi. 10.3310/RFTY4766
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- Publication type:
- Article
How Do We Safely Increase Day‐Case Tonsillectomy for the Treatment of Paediatric Obstructive Sleep Apnoea—A Cohort Analysis.
- Published in:
- Clinical Otolaryngology, 2024, v. 49, n. 6, p. 814, doi. 10.1111/coa.14200
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- Publication type:
- Article