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

Graciana Jaureguiberry

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Pediatric Nephrology (Berlin, Germany)|July 11, 2015
HNF1B-associated clinical phenotypes: the kidney and beyondDetlef Bockenhauer, Graciana Jaureguiberry
American Journal of Medical Genetics. Part A|February 24, 2011
Hereditary hypophosphatemic rickets with hypercalciuria and nephrolithiasis-identification of a novel SLC34A3/NaPi-IIc mutationPriya Phulwani, Clemens Bergwitz, Graciana Jaureguiberry, et al.
Pediatric Nephrology (Berlin, Germany)|November 4, 2015
Cyclophosphamide and rituximab in frequently relapsing/steroid-dependent nephrotic syndromeHazel Webb, Graciana Jaureguiberry, Stephanie Dufek, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 11, 2008
A patient with hypophosphatemia, a femoral fracture, and recurrent kidney stones: report of a novel mutation in SLC34A3Kathleen Page, Clemens Bergwitz, Graciana Jaureguiberry, et al.
American Journal of Physiology. Renal Physiology|May 16, 2008
A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets with hypercalciuria in humans identifies threonine 137 as an important determinant of sodium-phosphate cotransport in NaPi-IIcGraciana Jaureguiberry, Thomas O Carpenter, Stuart Forman, et al.
Pediatric Nephrology (Berlin, Germany)|February 9, 2011
A patient with polyuria and hydronephrosis: questionGraciana Jaureguiberry, William Van't Hoff, Imran Mushtaq, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2011
Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutationsStephen D Marks, Ambrose M Gullett, Eileen Brennan, et al.
Physiological Reports|December 27, 2021
Quantification of FAM20A in human milk and identification of calcium metabolism proteinsVaksha Patel, Enriko Klootwijk, Gail Whiting, et al.
The New England Journal of Medicine|January 10, 2014
Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndromeEnriko D Klootwijk, Markus Reichold, Amanda Helip-Wooley, et al.
Journal of the American Society of Nephrology : JASN|February 12, 2022
A Founder Mutation in <i>EHD1</i> Presents with Tubular Proteinuria and DeafnessNaomi Issler, Sara Afonso, Irith Weissman, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Pediatric Nephrology (Berlin, Germany)|July 11, 2015
HNF1B-associated clinical phenotypes: the kidney and beyondDetlef Bockenhauer, Graciana Jaureguiberry
American Journal of Medical Genetics. Part A|February 24, 2011
Hereditary hypophosphatemic rickets with hypercalciuria and nephrolithiasis-identification of a novel SLC34A3/NaPi-IIc mutationPriya Phulwani, Clemens Bergwitz, Graciana Jaureguiberry, et al.
Pediatric Nephrology (Berlin, Germany)|November 4, 2015
Cyclophosphamide and rituximab in frequently relapsing/steroid-dependent nephrotic syndromeHazel Webb, Graciana Jaureguiberry, Stephanie Dufek, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 11, 2008
A patient with hypophosphatemia, a femoral fracture, and recurrent kidney stones: report of a novel mutation in SLC34A3Kathleen Page, Clemens Bergwitz, Graciana Jaureguiberry, et al.
American Journal of Physiology. Renal Physiology|May 16, 2008
A novel missense mutation in SLC34A3 that causes hereditary hypophosphatemic rickets with hypercalciuria in humans identifies threonine 137 as an important determinant of sodium-phosphate cotransport in NaPi-IIcGraciana Jaureguiberry, Thomas O Carpenter, Stuart Forman, et al.
Pediatric Nephrology (Berlin, Germany)|February 9, 2011
A patient with polyuria and hydronephrosis: questionGraciana Jaureguiberry, William Van't Hoff, Imran Mushtaq, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2011
Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutationsStephen D Marks, Ambrose M Gullett, Eileen Brennan, et al.
Physiological Reports|December 27, 2021
Quantification of FAM20A in human milk and identification of calcium metabolism proteinsVaksha Patel, Enriko Klootwijk, Gail Whiting, et al.
The New England Journal of Medicine|January 10, 2014
Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndromeEnriko D Klootwijk, Markus Reichold, Amanda Helip-Wooley, et al.
Journal of the American Society of Nephrology : JASN|February 12, 2022
A Founder Mutation in <i>EHD1</i> Presents with Tubular Proteinuria and DeafnessNaomi Issler, Sara Afonso, Irith Weissman, et al.
Pageof 2