Vianna, J. G. P., Simor, T. G., Senna, P., De Bortoli, M. R., Costalonga, E. F., Seguro, A. C., & Luchi, W. M. (2019). Atypical presentation of familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a patient with a new claudin-16 gene mutation. Clin Nephrol Case Stud.

Vianna, Júlia Guasti P., Thiago Gabriel Simor, Pamella Senna, Michell Roncete De Bortoli, Everlayny Fiorot Costalonga, Antonio Carlos Seguro, and Weverton Machado Luchi. "Atypical Presentation of Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis in a Patient With a New Claudin-16 Gene Mutation." Clin Nephrol Case Stud 2019.

Vianna, Júlia Guasti P., et al. "Atypical Presentation of Familial Hypomagnesemia With Hypercalciuria and Nephrocalcinosis in a Patient With a New Claudin-16 Gene Mutation." Clin Nephrol Case Stud 2019.