Litcius/Paper detail

Autosomal dominant ApoA4 mutations present as tubulointerstitial kidney disease with medullary amyloidosis

Tereza Kmochová, Kendrah Kidd, Andrew Orr, Aleš Hnı́zda, Hana Hartmannová, Kateřina Hodaňová, Petr Vyleťal, Karolína Naušová, Vítězslav Brinsa, Helena Trešlová, Jana Sovová, Veronika Barešová, Klára Svojšová, Alena Vrbacká, Viktor Stránecký, Victoria Robins, Abbigail Taylor, Lauren Martin, Ana Rivas-Chavez, Riley Payne, Heidi A. Bleyer, Adrienne H. Williams, Helmut G. Rennke, Astrid Weins, Patrick Short, Varun Agrawal, Leroy Storsley, Sushrut S. Waikar, Ellen D. McPhail, Surendra Dasari, Nelson Leung, Tom Hewlett, Jake Yorke, Daniel Gaston, Laurette Geldenhuys, Mark E. Samuels, Adam P. Levine, Michael L. West, Helena Hůlková, Petr Pompach, Petr Novák, Richard B. Weinberg, Karen Bedard, Martina Živná, Jakub Sikora, Anthony J. Bleyer, Stanislav Kmoch

2023Kidney International18 citationsDOIOpen Access PDF

Topics & Concepts

Medullary cavityAmyloidosisPathologyKidneyKidney diseaseMutationDiseaseMedicineBiologyGeneticsInternal medicineGeneAmyloidosis: Diagnosis, Treatment, OutcomesChronic Kidney Disease and DiabetesRenal Diseases and Glomerulopathies