Autosomal dominant polycystic kidney disease: risk factor for nonmelanoma skin cancer following kidney transplantation
Anne Bretagnol, Matthias Büchler(Centre Hospitalier Universitaire de Tours), Yvon Lebranchu(Académie Nationale de Médecine), Jean‐Michel Halimi(Centre Hospitalier Universitaire de Tours), Christelle Barbet(Centre Hospitalier Régional Universitaire de Brest), J Badin, Jean Frédéric Marlière(Université de Tours), Mélanie Roland(Centre Hospitalier Universitaire de Tours), Hubert Nivet(Centre Hospitalier Universitaire de Tours), Azmi Al Najjar(Centre Hospitalier Universitaire de Tours), L. Machet(Université de Tours)
Cited by 26
Related Papers
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination
|Nature Genetics|2003|643
Enteral versus parenteral early nutrition in ventilated adults with shock: a randomised, controlled, multicentre, open-label, parallel-group study (NUTRIREA-2)
|The Lancet|2017|568
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
|Nature Genetics|2007|495
Immunoprophylaxis with Basiliximab Compared with Antithymocyte Globulin in Renal Transplant Patients Receiving MMF-containing Triple Therapy
|American Journal of Transplantation|2002|256
Spectrum of Mutations in Gitelman Syndrome
|Journal of the American Society of Nephrology|2011|239