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

Miguel Verbitsky

Showing results (21-30 of 49) with videos related to

Pageof 5
Sort By:
JCI Insight|December 9, 2025
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral refluxMiguel Verbitsky, Pavan Khosla, Daniel Bivona, et al.
Pediatric Nephrology (Berlin, Germany)|January 14, 2026
APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tractLisanne M Vendrig, Juntao Ke, Michael W T Tanck, et al.
Journal of the American Society of Nephrology : JASN|October 27, 2022
Genomic Disorders in CKD across the LifespanMiguel Verbitsky, Sarathbabu Krishnamurthy, Priya Krithivasan, et al.
Annals of Internal Medicine|December 6, 2017
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot StudySneh Lata, Maddalena Marasa, Yifu Li, et al.
The Journal of Clinical Investigation|March 28, 2025
Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathySindhuri Prakash, Nicholas J Steers, Yifu Li, et al.
The Journal of Clinical Investigation|June 15, 2026
Erratum to Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathySindhuri Prakash, Nicholas J Steers, Yifu Li, et al.
Archives of Neurology|September 15, 2010
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease studyRoy N Alcalay, Elise Caccappolo, Helen Mejia-Santana, et al.
Archives of Neurology|December 17, 2009
Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson diseaseRoy N Alcalay, Helen Mejia-Santana, Ming Xin Tang, et al.
Journal of Clinical and Experimental Neuropsychology|February 26, 2010
Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's diseaseRoy N Alcalay, Helen Mejia-Santana, Ming X Tang, et al.
The Journal of Clinical Investigation|September 3, 2024
Increased risk of kidney failure in patients with genetic kidney disordersMark D Elliott, Natalie Vena, Maddalena Marasa, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
JCI Insight|December 9, 2025
Urobiota analysis and genome-wide association study in pediatric recurrent urinary tract infections and vesicoureteral refluxMiguel Verbitsky, Pavan Khosla, Daniel Bivona, et al.
Pediatric Nephrology (Berlin, Germany)|January 14, 2026
APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tractLisanne M Vendrig, Juntao Ke, Michael W T Tanck, et al.
Journal of the American Society of Nephrology : JASN|October 27, 2022
Genomic Disorders in CKD across the LifespanMiguel Verbitsky, Sarathbabu Krishnamurthy, Priya Krithivasan, et al.
Annals of Internal Medicine|December 6, 2017
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot StudySneh Lata, Maddalena Marasa, Yifu Li, et al.
The Journal of Clinical Investigation|March 28, 2025
Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathySindhuri Prakash, Nicholas J Steers, Yifu Li, et al.
The Journal of Clinical Investigation|June 15, 2026
Erratum to Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathySindhuri Prakash, Nicholas J Steers, Yifu Li, et al.
Archives of Neurology|September 15, 2010
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease studyRoy N Alcalay, Elise Caccappolo, Helen Mejia-Santana, et al.
Archives of Neurology|December 17, 2009
Motor phenotype of LRRK2 G2019S carriers in early-onset Parkinson diseaseRoy N Alcalay, Helen Mejia-Santana, Ming Xin Tang, et al.
Journal of Clinical and Experimental Neuropsychology|February 26, 2010
Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's diseaseRoy N Alcalay, Helen Mejia-Santana, Ming X Tang, et al.
The Journal of Clinical Investigation|September 3, 2024
Increased risk of kidney failure in patients with genetic kidney disordersMark D Elliott, Natalie Vena, Maddalena Marasa, et al.
Pageof 5