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

Carla G Monico

Showing results (1-10 of 13) with videos related to

Pageof 2
Sort By:
Nature Reviews. Nephrology|December 21, 2011
Genetic determinants of urolithiasisCarla G Monico, Dawn S Milliner
American Journal of Nephrology|April 26, 2005
Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluriaCarla G Monico, Julie B Olson, Dawn S Milliner
Kidney International|April 21, 2005
Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant alleleCarla G Monico, Sandro Rossetti, Julie B Olson, et al.
Kidney International|July 12, 2002
Potential mechanisms of marked hyperoxaluria not due to primary hyperoxaluria I or IICarla G Monico, Mai Persson, G Charles Ford, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 7, 2006
Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2John Knight, Ross P Holmes, Dawn S Milliner, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 6, 2010
Cardiac abnormalities in primary hyperoxaluriaFarouk Mookadam, Travis Smith, Panupong Jiamsripong, et al.
American Journal of Medical Genetics. Part A|July 24, 2012
Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation in AGXT and a terminal deletion of chromosome 2Rachaneekorn Tammachote, Nelawat Kingsuwannapong, Siraprapa Tongkobpetch, et al.
Journal of the American Society of Nephrology : JASN|April 27, 2007
Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosisCarla G Monico, Sandro Rossetti, Heidi A Schwanz, et al.
American Journal of Nephrology|June 18, 2005
International registry for primary hyperoxaluriaJohn C Lieske, Carla G Monico, W Scott Holmes, et al.
Human Mutation|May 30, 2009
Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT geneEmma L Williams, Cecile Acquaviva, Antonio Amoroso, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Nature Reviews. Nephrology|December 21, 2011
Genetic determinants of urolithiasisCarla G Monico, Dawn S Milliner
American Journal of Nephrology|April 26, 2005
Implications of genotype and enzyme phenotype in pyridoxine response of patients with type I primary hyperoxaluriaCarla G Monico, Julie B Olson, Dawn S Milliner
Kidney International|April 21, 2005
Pyridoxine effect in type I primary hyperoxaluria is associated with the most common mutant alleleCarla G Monico, Sandro Rossetti, Julie B Olson, et al.
Kidney International|July 12, 2002
Potential mechanisms of marked hyperoxaluria not due to primary hyperoxaluria I or IICarla G Monico, Mai Persson, G Charles Ford, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 7, 2006
Glyoxylate reductase activity in blood mononuclear cells and the diagnosis of primary hyperoxaluria type 2John Knight, Ross P Holmes, Dawn S Milliner, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|October 6, 2010
Cardiac abnormalities in primary hyperoxaluriaFarouk Mookadam, Travis Smith, Panupong Jiamsripong, et al.
American Journal of Medical Genetics. Part A|July 24, 2012
Primary hyperoxaluria type 1 and brachydactyly mental retardation syndrome caused by a novel mutation in AGXT and a terminal deletion of chromosome 2Rachaneekorn Tammachote, Nelawat Kingsuwannapong, Siraprapa Tongkobpetch, et al.
Journal of the American Society of Nephrology : JASN|April 27, 2007
Comprehensive mutation screening in 55 probands with type 1 primary hyperoxaluria shows feasibility of a gene-based diagnosisCarla G Monico, Sandro Rossetti, Heidi A Schwanz, et al.
American Journal of Nephrology|June 18, 2005
International registry for primary hyperoxaluriaJohn C Lieske, Carla G Monico, W Scott Holmes, et al.
Human Mutation|May 30, 2009
Primary hyperoxaluria type 1: update and additional mutation analysis of the AGXT geneEmma L Williams, Cecile Acquaviva, Antonio Amoroso, et al.
Pageof 2