Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Daniel G Bichet

Showing results (11-20 of 144) with videos related to

Pageof 15
Sort By:
Swiss Medical Weekly|July 18, 2012
Physiopathology of hereditary polyuric states: a molecular view of renal functionDaniel G Bichet
Annual Review of Physiology|February 12, 2019
Regulation of Thirst and Vasopressin ReleaseDaniel G Bichet
Clinical Kidney Journal|April 9, 2015
Central vasopressin: dendritic and axonal secretion and renal actionsDaniel G Bichet
European Journal of Endocrinology|June 25, 2020
GENETICS IN ENDOCRINOLOGY Pathophysiology, diagnosis and treatment of familial nephrogenic diabetes insipidusDaniel G Bichet
Kidney International|November 7, 2012
A defect in vasopressin secretion in autosomal dominant polycystic kidney diseaseDaniel G Bichet
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 18, 2010
Kidney and liver cysts in autosomal dominant polycystic kidney diseaseDaniel G Bichet
Progress in Molecular Biology and Translational Science|April 9, 2010
V2R mutations and nephrogenic diabetes insipidusDaniel G Bichet
The New England Journal of Medicine|October 20, 2021
Aquaporin-1 Expression and Ultrafiltration of the Peritoneal MembraneDaniel G Bichet
Kidney International|February 10, 2025
Thirsty encounters of the third kindDaniel G Bichet, Detlef Bockenhauer
Best Practice & Research. Clinical Endocrinology & Metabolism|May 10, 2016
Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant)Daniel G Bichet, Detlef Bockenhauer
Pageof 15

Showing results (11-20 of 144) with videos related to

Sort By:
Pageof 15
Swiss Medical Weekly|July 18, 2012
Physiopathology of hereditary polyuric states: a molecular view of renal functionDaniel G Bichet
Annual Review of Physiology|February 12, 2019
Regulation of Thirst and Vasopressin ReleaseDaniel G Bichet
Clinical Kidney Journal|April 9, 2015
Central vasopressin: dendritic and axonal secretion and renal actionsDaniel G Bichet
European Journal of Endocrinology|June 25, 2020
GENETICS IN ENDOCRINOLOGY Pathophysiology, diagnosis and treatment of familial nephrogenic diabetes insipidusDaniel G Bichet
Kidney International|November 7, 2012
A defect in vasopressin secretion in autosomal dominant polycystic kidney diseaseDaniel G Bichet
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 18, 2010
Kidney and liver cysts in autosomal dominant polycystic kidney diseaseDaniel G Bichet
Progress in Molecular Biology and Translational Science|April 9, 2010
V2R mutations and nephrogenic diabetes insipidusDaniel G Bichet
The New England Journal of Medicine|October 20, 2021
Aquaporin-1 Expression and Ultrafiltration of the Peritoneal MembraneDaniel G Bichet
Kidney International|February 10, 2025
Thirsty encounters of the third kindDaniel G Bichet, Detlef Bockenhauer
Best Practice & Research. Clinical Endocrinology & Metabolism|May 10, 2016
Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant)Daniel G Bichet, Detlef Bockenhauer
Pageof 15