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The Journal of Clinical Endocrinology and Metabolism
|
June 7, 2002
Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families
Shih-Hua Lin, Daniel G Bichet, Sei Sasaki, et al.
Nephron. Physiology
|
October 10, 2009
Vasopressin type 2 receptor V88M mutation: molecular basis of partial and complete nephrogenic diabetes insipidus
Detlef Bockenhauer, Eric Carpentier, Driss Rochdi, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
March 29, 2002
Intrafamilial phenotype variability in nephrogenic diabetes insipidus
Karine Kalenga, Alexandre Persu, Eric Goffin, et al.
Drugs in R&D
|
September 20, 2021
The Safety of Agalsidase Alfa Enzyme Replacement Therapy in Canadian Patients with Fabry Disease Following Implementation of a Bioreactor Process
Aneal Khan, Sandra M Sirrs, Daniel G Bichet, et al.
Scientific Reports
|
June 26, 2019
Disease-linked mutations alter the stoichiometries of HCN-KCNE2 complexes
Yoann Lussier, Oliver Fürst, Eva Fortea, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 9, 2011
A patient with polyuria and hydronephrosis: question
Graciana Jaureguiberry, William Van't Hoff, Imran Mushtaq, et al.
Clinical Kidney Journal
|
June 13, 2015
Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology
Daniel G Bichet, Abdulah El Tarazi, Jessica Matar, et al.
Journal of the American Society of Nephrology : JASN
|
February 27, 2010
Oral tolvaptan is safe and effective in chronic hyponatremia
Tomas Berl, Friederike Quittnat-Pelletier, Joseph G Verbalis, et al.
Pediatric Nephrology (Berlin, Germany)
|
March 19, 2009
Wilms tumor arising in a child with X-linked nephrogenic diabetes insipidus
Reyhan El-Kares, Pierre-Alain Hueber, Miriam Blumenkrantz, et al.
Critical Reviews in Clinical Laboratory Sciences
|
March 18, 2024
G protein-coupled receptor (GPCR) gene variants and human genetic disease
Miles D Thompson, Maire E Percy, David E C Cole, et al.
Page
of 15
Search research articles
Search
Showing results (71-80 of 144) with videos related to
Sort By:
Page
of 15
The Journal of Clinical Endocrinology and Metabolism
|
June 7, 2002
Two novel aquaporin-2 mutations responsible for congenital nephrogenic diabetes insipidus in Chinese families
Shih-Hua Lin, Daniel G Bichet, Sei Sasaki, et al.
Nephron. Physiology
|
October 10, 2009
Vasopressin type 2 receptor V88M mutation: molecular basis of partial and complete nephrogenic diabetes insipidus
Detlef Bockenhauer, Eric Carpentier, Driss Rochdi, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
March 29, 2002
Intrafamilial phenotype variability in nephrogenic diabetes insipidus
Karine Kalenga, Alexandre Persu, Eric Goffin, et al.
Drugs in R&D
|
September 20, 2021
The Safety of Agalsidase Alfa Enzyme Replacement Therapy in Canadian Patients with Fabry Disease Following Implementation of a Bioreactor Process
Aneal Khan, Sandra M Sirrs, Daniel G Bichet, et al.
Scientific Reports
|
June 26, 2019
Disease-linked mutations alter the stoichiometries of HCN-KCNE2 complexes
Yoann Lussier, Oliver Fürst, Eva Fortea, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 9, 2011
A patient with polyuria and hydronephrosis: question
Graciana Jaureguiberry, William Van't Hoff, Imran Mushtaq, et al.
Clinical Kidney Journal
|
June 13, 2015
Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology
Daniel G Bichet, Abdulah El Tarazi, Jessica Matar, et al.
Journal of the American Society of Nephrology : JASN
|
February 27, 2010
Oral tolvaptan is safe and effective in chronic hyponatremia
Tomas Berl, Friederike Quittnat-Pelletier, Joseph G Verbalis, et al.
Pediatric Nephrology (Berlin, Germany)
|
March 19, 2009
Wilms tumor arising in a child with X-linked nephrogenic diabetes insipidus
Reyhan El-Kares, Pierre-Alain Hueber, Miriam Blumenkrantz, et al.
Critical Reviews in Clinical Laboratory Sciences
|
March 18, 2024
G protein-coupled receptor (GPCR) gene variants and human genetic disease
Miles D Thompson, Maire E Percy, David E C Cole, et al.
Page
of 15