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 (11-20 of 16) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 16 results.
Human Molecular Genetics|August 1, 1997
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disordersS E Lloyd, W Gunther, S H Pearce, et al.
Kidney International|January 5, 2000
Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuriaS J Scheinman, J P Cox, S E Lloyd, et al.
QJM : Monthly Journal of the Association of Physicians|August 25, 2012
Tropical distal renal tubular acidosis: clinical and epidemiological studies in 78 patientsS Khositseth, L J Bruce, S B Walsh, et al.
Nature|February 1, 1996
A common molecular basis for three inherited kidney stone diseasesS E Lloyd, S H Pearce, S E Fisher, et al.
The Biochemical Journal|August 6, 2000
Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cellsL J Bruce, O Wrong, A M Toye, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 1998
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosisF E Karet, F J Gainza, A Z Györy, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Human Molecular Genetics|August 1, 1997
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disordersS E Lloyd, W Gunther, S H Pearce, et al.
Kidney International|January 5, 2000
Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuriaS J Scheinman, J P Cox, S E Lloyd, et al.
QJM : Monthly Journal of the Association of Physicians|August 25, 2012
Tropical distal renal tubular acidosis: clinical and epidemiological studies in 78 patientsS Khositseth, L J Bruce, S B Walsh, et al.
Nature|February 1, 1996
A common molecular basis for three inherited kidney stone diseasesS E Lloyd, S H Pearce, S E Fisher, et al.
The Biochemical Journal|August 6, 2000
Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cellsL J Bruce, O Wrong, A M Toye, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 1998
Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosisF E Karet, F J Gainza, A Z Györy, et al.
Pageof 2