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161 Possible Causes for chauveau

  • Familial Juvenile Hyperuricemic Nephropathy Type 1

    Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, Buchler M, Cochat P, Cosyns JP, Mougenot B, Rider MH, Antignac C[karger.com] Pediatr Nephrol. 1993; 7 :105–18. [ PubMed : 8439471 ] Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, Buchler M[ncbi.nlm.nih.gov] J Am Soc Nephrol. 2001; 12 :2348–57. [ PubMed : 11675411 ] Eckardt K-U, Alper SL, Antignac C, Bleyer AJ, Chauveau D, Dahan K, Deltas C, Hosking A, Kmoch S, Rampoldi L, Wiesener[ncbi.nlm.nih.gov]

  • Familial Juvenile Hyperuricemic Nephropathy 3

    Pediatr Nephrol. 1993; 7 :105–18. [ PubMed : 8439471 ] Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, Buchler M[ncbi.nlm.nih.gov] JOURNAL ARTICLES Eckardt KU, Alper SL, Antignac C, Bleyer AJ, Chauveau D, Dahan K, Deltas C, Hosking A, Kmoch S, Rampoldi L, Wiesener M, Wolf MT, Devuyst O: Autosomal dominant[rarediseases.org] Calado, Gaspar, Clemente, Rueff, Lens, Banet, Outeda, Barrio-Lucía, Dahan, Devuyst, Smaers, Vertommen, Loute, Poux, Viron, Jacquot, Gagnadoux, Chauveau, Büchler, Cochat, Cosyns[wikigenes.org]

  • Familial Juvenile Hyperuricemic Nephropathy Type 2

    Pediatr Nephrol. 1993; 7 :105–18. [ PubMed : 8439471 ] Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, Buchler M[ncbi.nlm.nih.gov] JOURNAL ARTICLES Eckardt KU, Alper SL, Antignac C, Bleyer AJ, Chauveau D, Dahan K, Deltas C, Hosking A, Kmoch S, Rampoldi L, Wiesener M, Wolf MT, Devuyst O: Autosomal dominant[rarediseases.org] Calado , Gaspar , Clemente , Rueff , Lens , Banet , Outeda , Barrio-Lucía , Dahan , Devuyst , Smaers , Vertommen , Loute , Poux , Viron , Jacquot , Gagnadoux , Chauveau ,[wikigenes.org]

  • Antenatal Onset Minicore Myopathy with Arthrogryposis

    DOI: 10.1093/hmg/ddt494 Vancouver Chauveau C, Bonnemann CG, Julien C , Kho AL , Marks H, Talim B et al.[kclpure.kcl.ac.uk] Human Molecular Genetics , Feb 2014 Claire Chauveau , Carsten G.[paperity.org] DOI: 10.1093/hmg/ddt494 APA Chauveau, C., Bonnemann, C. G., Julien, C. , Kho, A. L. , Marks, H., Talim, B., ... Ferreiro, A. (2014).[kclpure.kcl.ac.uk]

  • Secondary Polyarteritis nodosa

    Chauveau D, Christophe JL. Images in clinical medicine. Renal aneurysms in hepatitis B-associated polyarteritis nodosa. N Engl J Med 1995;332:1070.[indianjurol.com]

  • Hypokalemic Periodic Paralysis

    Sternberg D, Maisonobe T, Jurkat-Rott K, Nicole S, Launay E, Chauveau D, Tabti N, Lehmann-Horn F, Hainque B, Fontaine B.[doi.org] Curr Opin Pharmacol. 2001; 1 :280–7. [ PubMed : 11712752 ] Jurkat-Rott K, Mitrovic N, Hang C, Kouzmekine A, Iaizzo P, Herzog J, Lerche H, Nicole S, Vale-Santos J, Chauveau[ncbi.nlm.nih.gov] Jurkat-Rott K, Mitrovic N, Hang C, Kouzmekine A, Iaizzo P, Herzog J, Lerche H, Nicole S, Vale-Santos J, Chauveau D, Fontaine B, Lehmann-Horn F.[doi.org]

  • Adult Polycystic Kidney Disease Type 1

    Pirson Y, Chauveau D, Torres V: Management of cerebral aneurysms in autosomal dominant polycystic kidney disease. J Am Soc Nephrol 13:269–276, 2002.[link.springer.com] Chauveau, D. et al. Intracranial aneurysms in autosomal dominant polycystic kidney disease. Kidney Int. 45, 1140–1146 (1994). 86. Rinkel, G. J.[nature.com] Persu A, El-Khattabi O, Messiaen T, Pirson Y, Chauveau D, Devuyst O.[ajpb.com]

  • Familial Interstitial Nephritis

    JOURNAL ARTICLES Eckardt KU, Alper SL, Antignac C, Bleyer AJ, Chauveau D, Dahan K, Deltas C, Hosking A, Kmoch S, Rampoldi L, Wiesener M, Wolf MT, Devuyst O: Autosomal dominant[rarediseases.org] ICD-11: GB82 ICD-10: N15 E79.0 Q61.5 MeSH: C537696 OMIM: 162000 603860 174000 613092 617056 137920 125853 文献 PMID: 25738250 著者 Eckardt KU, Alper SL, Antignac C, Bleyer AJ, Chauveau[genome.jp] View Article PubMed PubMed Central Google Scholar Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, Buchler M, Cochat[bmcmedgenet.biomedcentral.com]

  • Medullary Cystic Kidney Disease

    16p12.3); HNF1B encoding hepatocyte nuclear factor-1β (chromosome 17q12); and REN encoding renin (chromosome 1q32.1). a b Eckardt, KU; Alper, SL; Antignac, C; Bleyer, AJ; Chauveau[en.wikipedia.org] Pediatr Nephrol. 1993; 7 :105–18. [ PubMed : 8439471 ] Dahan K, Devuyst O, Smaers M, Vertommen D, Loute G, Poux JM, Viron B, Jacquot C, Gagnadoux MF, Chauveau D, Buchler M[ncbi.nlm.nih.gov] Rossetti S, Kubly VJ, Consugar MB, Hopp K, Roy S, Horsley SW, Chauveau D, Rees L, Barratt TM, van’t Hoff WG, Niaudet WP, Torres VE, Harris PC (2009) Incompletely penetrant[link.springer.com]

  • Polycystic Kidney Disease

    In ADPKD liver cysts develop later than kidney cysts, with a steady increase in frequency with advancing age, and are more common in women ( Chauveau 2000 ).[doi.org] Rossetti S , Chauveau D , Walker D et al : A complete mutation screen of the ADPKD genes by DHPLC . Kidney Int 2002; 61 : 1588–1599. 40.[nature.com] J Comput Assisted Tomogr 24 : 614 –619, 2000 Rossetti S, Chauveau D, Walker D, Saggar-Malik A, Winearls CG, Torres VE, Harris PC: A complete mutation screen of the ADPKD genes[jasn.asnjournals.org]

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