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181 Possible Causes for niaudet

  • Frasier Syndrome

    Rein en Développement et Néphropathies Héréditdires, INSERM U 423, Hôpital Necker Enfants Malades, Paris, France Patrick Niaudet & Marie-Claire Gubler Néphrologie, Hôpital[doi.org] Niaudet P, Gubler MC. WT1 and glomerular diseases. Pediatr Nephrol. 2006 Nov;21(11):1653-60. Epub 2006 Aug 23. Review.[ghr.nlm.nih.gov] Barbaux S, Niaudet P, Gubler MC, Grunfeld JP, Jaubert F, Kuttenn F, Fekete CN, Souleyreau-Therville N, Thibaud E, Fellous M, McElreavey K.[humpath.com]

  • Oligomeganephronia

    PAX2 renal development renal hypoplasia retinal defects renal-coloboma syndrome References Salomon R, Tellier AL, Attie-Bitach T, Amiel J, Vekemans M, Lyonnet S, Dureau P, Niaudet[humpath.com] . , Niaudet P. , Gubler M.-C. , Broyer M. BACKGROUND: Oligomeganephronia (OMN) is a rare congenital and usually sporadic anomaly.[uniprot.org]

  • Congenital Nephrotic Syndrome Type 1

    Niaudet, P. Congenital nephrotic syndrome, Finnish type. Orphanet . February 2007; . Accessed 12/6/2016.[rarediseases.info.nih.gov] Niaudet P. Congenital and infantile nephrotic syndrome. UpToDate, Inc. website. Accessed May 24, 2017. Hall G, Winn MP. Inherited Causes of Nephrotic Syndrome.[thinkgenetic.com] Pediatr Clin North Am 42: 1459–1468 CrossRef PubMed Google Scholar Niaudet P (2004) Genetic forms of nephrotic syndrome.[link.springer.com]

  • Congenital Nephrotic Syndrome

    Niaudet P (2004) Genetic forms of nephrotic syndrome. Pediatr Nephrol 19:1313–1318 PubMed CrossRef Google Scholar 5.[doi.org] Niaudet, P. Congenital nephrotic syndrome, Finnish type. Orphanet . February 2007; . Accessed 12/6/2016.[rarediseases.info.nih.gov] Niaudet P. [Congenital and infantile nephrotic syndrome]. Nephrol Ther 2005;1:63–70. Crossref PubMed Google Scholar 2. Indumathi CK, Dinakar C, Lewin S, Phadke KD.[degruyter.com]

  • Nephronophthisis

    . & Niaudet, P. Nephronophthisis. Pediatr Nephrol, 2009 , 24 , 2333-2344[urology-textbook.com] Harmon, Patrick Niaudet, Norishige Yoshikawa[books.google.com] Salomon R, Saunier S, Niaudet P. Nephronophthisis. Pediatr Nephrol. 2009;24:2333–2344. 10. Waldherr R, Lennert T, Weber HP, et al. The nephronophthisis complex.[neocyst.de]

  • Nephronophthisis

    . & Niaudet, P. Nephronophthisis. Pediatr Nephrol, 2009 , 24 , 2333-2344[urology-textbook.com] Harmon, Patrick Niaudet, Norishige Yoshikawa[books.google.com] Salomon R, Saunier S, Niaudet P. Nephronophthisis. Pediatr Nephrol. 2009;24:2333–2344. 10. Waldherr R, Lennert T, Weber HP, et al. The nephronophthisis complex.[neocyst.de]

  • Autosomal Recessive Steroid-Resistant Nephrotic Syndrome

    Niaudet P, Gubler MC, Antignac C (2001) Molecular genetics of FSGS (abstract). Pediatr Nephrol 16:C31 Google Scholar 9.[link.springer.com] Avner ED, Harmon WE, Niaudet P, Yoshikawa N, eds. 2009 Springer-Verlag, Berlin, Germany. Pp. 643-666. Lifton RP, Somlo S, Giebisch GH, Seldin DW.[rarediseases.org] Barbaux S, Niaudet P, Gubler MC, Grünfeld JP, Jaubert F, Kuttenn F, Fekete CN, Souleyreau-Therville N, Thibaud E, Fellous M, McElreavey K (1997) Donor splice-site mutations[springermedizin.de]

  • Denys Drash Syndrome

    Jeanpierre C, Beroud C, Niaudet P, Junien C (1998) Software and database for the analysis of mutations in the human WT1 gene.[doi.org] PMID 9590178 WT1 and glomerular diseases Niaudet P, Gubler MC Pediatr Nephrol 2006; 21(11):1653-60.[atlasgeneticsoncology.org] Niaudet P, Gubler MC. WT1 and glomerular diseases. Pediatr Nephrol. 2006 Nov;21(11):1653-60. Epub 2006 Aug 23. Review.[ghr.nlm.nih.gov]

  • Nephronophthisis

    . & Niaudet, P. Nephronophthisis. Pediatr Nephrol, 2009 , 24 , 2333-2344[urology-textbook.com] Harmon, Patrick Niaudet, Norishige Yoshikawa[books.google.com] Salomon R, Saunier S, Niaudet P. Nephronophthisis. Pediatr Nephrol. 2009;24:2333–2344. 10. Waldherr R, Lennert T, Weber HP, et al. The nephronophthisis complex.[neocyst.de]

  • Congenital Nephrotic Syndrome Type Finnish

    Niaudet P. Congenital nephrotic syndrome, Finnish type. OrphaNet website. Accessed June 20, 2017.[thinkgenetic.com] Niaudet, P. Congenital nephrotic syndrome, Finnish type. Orphanet . February 2007; . Accessed 12/6/2016.[rarediseases.info.nih.gov] Pediatr Clin North Am 42: 1459–1468 CrossRef PubMed Google Scholar Niaudet P (2004) Genetic forms of nephrotic syndrome.[link.springer.com]

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