Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus—update and epidemiology

por Bichet, Daniel G., El Tarazi, Abdulah, Matar, Jessica, Lussier, Yoann, Arthus, Marie-Françoise, Lonergan, Michèle, Bockenhauer, Detlef, Bissonnette, Pierre
Publicado 2012

Long-term outcome in inherited nephrogenic diabetes insipidus

por Sharma, Sonia, Ashton, Emma, Iancu, Daniela, Arthus, Marie-Francoise, Hayes, Wesley, van’t Hoff, William, Kleta, Robert, Bichet, Daniel G, Bockenhauer, Detlef
Publicado 2018

Long-term outcome in inherited nephrogenic diabetes insipidus

por Sharma, Sonia, Ashton, Emma, Iancu, Daniela, Arthus, Marie-Francoise, Hayes, Wesley, van’t Hoff, William, Kleta, Robert, Bichet, Daniel G, Bockenhauer, Detlef
Publicado 2020

Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus

por Kamsteeg, Erik-Jan, Bichet, Daniel G., Konings, Irene B.M., Nivet, Hubert, Lonergan, Michelle, Arthus, Marie-Françoise, van Os, Carel H., Deen, Peter M.T.
Publicado 2003

Further evidence for functional recovery of AQP2 mutations associated with nephrogenic diabetes insipidus

por Bissonnette, Pierre, Lussier, Yoann, Matar, Jessica, Leduc‐Nadeau, Alexandre, Da Cal, Sandra, Arthus, Marie‐Françoise, Unwin, Robert J., Steinke, Julia, Rangaswamy, Dharshan, Bichet, Daniel G.
Publicado 2021

Diurnal Variation of Urinary Fabry Disease Biomarkers during Enzyme Replacement Therapy Cycles

por Boutin, Michel, Lavoie, Pamela, Menkovic, Iskren, Toupin, Amanda, Abaoui, Mona, Elidrissi-Elawad, Maha, Arthus, Marie-Françoise, Fortier, Carole, Ménard, Claudia, Maranda, Bruno, Bichet, Daniel G., Auray-Blais, Christiane
Publicado 2020