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76 Possible Causes for fliegauf

  • Nephronophthisis

    ., 2000, 2002], but was later additionally localized to the cilia transition zone [Fliegauf et al., 2006].[doi.org] Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E,[disorders.eyes.arizona.edu] Fliegauf M, Horvath J, von Schnakenburg C, Olbrich H, Muller D, Thumfart J, Schermer B, Pazour GJ, Neumann HP, Zentgraf H, et al: Nephrocystin specifically localizes to the[doi.org]

  • Nephronophthisis

    ., 2000, 2002], but was later additionally localized to the cilia transition zone [Fliegauf et al., 2006].[doi.org] Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E,[disorders.eyes.arizona.edu] Fliegauf M, Horvath J, von Schnakenburg C, Olbrich H, Muller D, Thumfart J, Schermer B, Pazour GJ, Neumann HP, Zentgraf H, et al: Nephrocystin specifically localizes to the[doi.org]

  • Nephronophthisis

    ., 2000, 2002], but was later additionally localized to the cilia transition zone [Fliegauf et al., 2006].[dx.doi.org] Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E,[disorders.eyes.arizona.edu] Fliegauf M, Horvath J, von Schnakenburg C, Olbrich H, Muller D, Thumfart J, Schermer B, Pazour GJ, Neumann HP, Zentgraf H, et al: Nephrocystin specifically localizes to the[dx.doi.org]

  • Nephronophthisis

    ., 2000, 2002], but was later additionally localized to the cilia transition zone [Fliegauf et al., 2006].[dx.doi.org] Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E,[disorders.eyes.arizona.edu] Fliegauf M, Horvath J, von Schnakenburg C, Olbrich H, Muller D, Thumfart J, Schermer B, Pazour GJ, Neumann HP, Zentgraf H, et al: Nephrocystin specifically localizes to the[dx.doi.org]

  • Nephronophthisis

    ., 2000, 2002], but was later additionally localized to the cilia transition zone [Fliegauf et al., 2006].[dx.doi.org] Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E,[disorders.eyes.arizona.edu] Fliegauf M, Horvath J, von Schnakenburg C, Olbrich H, Muller D, Thumfart J, Schermer B, Pazour GJ, Neumann HP, Zentgraf H, et al: Nephrocystin specifically localizes to the[dx.doi.org]

  • Nephronophthisis

    ., 2000, 2002], but was later additionally localized to the cilia transition zone [Fliegauf et al., 2006].[doi.org] Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E,[disorders.eyes.arizona.edu] Fliegauf M, Horvath J, von Schnakenburg C, Olbrich H, Muller D, Thumfart J, Schermer B, Pazour GJ, Neumann HP, Zentgraf H, et al: Nephrocystin specifically localizes to the[doi.org]

  • Nephronophthisis 7

    Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E,[disorders.eyes.arizona.edu] Crossref , Medline , CAS , Google Scholar 25 Olbrich H , Fliegauf M , Hoefele J et al.[futuremedicine.com] Weber Der Nephrologe (2007) Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Heike Olbrich , Manfred Fliegauf[nature.com]

  • Renal-Hepatic-Pancreatic Dysplasia 1

    An association with NPHP3 has been described. [1] It was characterized in 1959. [2] [3] References [ edit ] Bergmann C, Fliegauf M, Brüchle NO, et al. (April 2008).[en.wikipedia.org] ., Fliegauf, M., Hoefele, J., Kispert, A., Otto, E., Volz, A., et al. (2003).[pubman.mpdl.mpg.de] 雑誌 J Mol Diagn 12:125-31 (2010) DOI: 10.2353/jmoldx.2010.090033 文献 PMID: 18371931 著者 Bergmann C, Fliegauf M, Bruchle NO, Frank V, Olbrich H, Kirschner J, Schermer B, Schmedding[genome.jp]

  • Kartagener Syndrome

    Hum Genet. 2006; 120 :171–8. [ PubMed : 16783569 ] Bukowy-Bieryłło Z, Ziętkiewicz E, Loges NT, Wittmer M, Geremek M, Olbrich H, Fliegauf M, Voelkel K, Rutkiewicz E, Rutland[ncbi.nlm.nih.gov] Crossref Medline Google Scholar 3 Fliegauf M, Olbrich H, Horvath J, Wildhaber JH, Zariwala MA, Kennedy M, Knowles MR, Omran H.[doi.org] Pediatr Pulmonol. 2008; 43 :514–6. [ PubMed : 18383332 ] Budny B, Chen W, Omran H, Fliegauf M, Tzschach A, Wisniewska M, Jensen LR, Raynaud M, Shoichet SA, Badura M, Lenzner[ncbi.nlm.nih.gov]

  • Senior Loken Syndrome

    Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E,[disorders.eyes.arizona.edu] J Am Soc Nephrol. 2007 May 18; PMID: 17513324 von Schnakenburg C, Fliegauf M, Omran H. Nephrocystin and ciliary defects not only in the kidney?[humpath.com] Olbrich H, Fliegauf M, Hoefele J, Kispert A, Otto E, Volz A, Wolf MT, Sasmaz G, Trauer U, Reinhardt R, Sudbrak R, Antignac C, Gretz N, Walz G, Schermer B, Benzing T, Hildebrandt[disorders.eyes.arizona.edu]

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