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

O Wrong

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
The American Journal of Clinical Nutrition|September 1, 1978
Nitrogen metabolism in the gutO Wrong
Pediatric Nephrology (Berlin, Germany)|March 1, 1991
Distal renal tubular acidosis: the value of urinary pH, PCO2 and NH4+ measurementsO Wrong
Clinical Nephrology|July 1, 1987
A study of immune responses to Tamm-Horsfall glycoprotein in the sera of patients with renal tubular acidosisF A Duffy, R D Marshall, O Wrong
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|June 3, 1999
The association between familial distal renal tubular acidosis and mutations in the red cell anion exchanger (band 3, AE1) geneL J Bruce, R J Unwin, O Wrong, et al.
Human Molecular Genetics|December 1, 1993
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22M A Pook, O Wrong, C Wooding, et al.
Human Molecular Genetics|November 1, 1994
Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis)S E Fisher, G C Black, S E Lloyd, et al.
Kidney International|January 5, 2000
Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseasesA G Norden, S J Scheinman, M M Deschodt-Lanckman, et al.
The Journal of Clinical Investigation|October 6, 1997
Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) geneL J Bruce, D L Cope, G K Jones, et al.
Kidney International|November 13, 2001
Glomerular protein sieving and implications for renal failure in Fanconi syndromeA G Norden, M Lapsley, P J Lee, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1999
Renal chloride channel, CLCN5, mutations in Dent's diseaseJ P Cox, K Yamamoto, P T Christie, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
The American Journal of Clinical Nutrition|September 1, 1978
Nitrogen metabolism in the gutO Wrong
Pediatric Nephrology (Berlin, Germany)|March 1, 1991
Distal renal tubular acidosis: the value of urinary pH, PCO2 and NH4+ measurementsO Wrong
Clinical Nephrology|July 1, 1987
A study of immune responses to Tamm-Horsfall glycoprotein in the sera of patients with renal tubular acidosisF A Duffy, R D Marshall, O Wrong
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|June 3, 1999
The association between familial distal renal tubular acidosis and mutations in the red cell anion exchanger (band 3, AE1) geneL J Bruce, R J Unwin, O Wrong, et al.
Human Molecular Genetics|December 1, 1993
Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22M A Pook, O Wrong, C Wooding, et al.
Human Molecular Genetics|November 1, 1994
Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis)S E Fisher, G C Black, S E Lloyd, et al.
Kidney International|January 5, 2000
Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseasesA G Norden, S J Scheinman, M M Deschodt-Lanckman, et al.
The Journal of Clinical Investigation|October 6, 1997
Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) geneL J Bruce, D L Cope, G K Jones, et al.
Kidney International|November 13, 2001
Glomerular protein sieving and implications for renal failure in Fanconi syndromeA G Norden, M Lapsley, P J Lee, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 1, 1999
Renal chloride channel, CLCN5, mutations in Dent's diseaseJ P Cox, K Yamamoto, P T Christie, et al.
Pageof 2