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

Danica Novacic

Showing results (1-10 of 9) with videos related to

Pageof 1
Sort By:
Kidney Medicine|August 1, 2020
SGLT2 Inhibitors for Treatment of Refractory Hypomagnesemia: A Case Report of 3 PatientsEvan C Ray, Cary R Boyd-Shiwarski, Pengfei Liu, et al.
Journal of the American Dietetic Association|March 31, 2009
Comparative effects of three popular diets on lipids, endothelial function, and C-reactive protein during weight maintenanceMichael Miller, Valerie Beach, John D Sorkin, et al.
BMC Nephrology|September 11, 2019
Case report: extreme coronary calcifications and hypomagnesemia in a patient with a 17q12 deletion involving HNF1BHoward J Li, Catherine Groden, Melanie P Hoenig, et al.
Rare (Amsterdam, Netherlands)|March 4, 2024
Calciphylaxis in POEMS syndrome: Case reportDanica Novacic, Thomas Uldrick, Alina Dulau-Florea, et al.
HGG Advances|March 11, 2026
Biallelic Variants in RNU6ATAC Result in a Minor Spliceopathy Characterized by Transcriptome-Wide Minor Intron Retention Events and Short Stature with Variable Multisystem ManifestationsRodrigo Mendez, Taylor M Arriaga, Jialan Ma, et al.
EMBO Molecular Medicine|April 4, 2023
Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stabilityDirenis Erdinc, Alejandro Rodríguez-Luis, Mahmoud R Fassad, et al.
American Journal of Human Genetics|July 3, 2018
De Novo Missense Variants in TRAF7 Cause Developmental Delay, Congenital Anomalies, and Dysmorphic FeaturesMari J Tokita, Chun-An Chen, David Chitayat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.
The New England Journal of Medicine|October 27, 2020
Somatic Mutations in <i>UBA1</i> and Severe Adult-Onset Autoinflammatory DiseaseDavid B Beck, Marcela A Ferrada, Keith A Sikora, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Kidney Medicine|August 1, 2020
SGLT2 Inhibitors for Treatment of Refractory Hypomagnesemia: A Case Report of 3 PatientsEvan C Ray, Cary R Boyd-Shiwarski, Pengfei Liu, et al.
Journal of the American Dietetic Association|March 31, 2009
Comparative effects of three popular diets on lipids, endothelial function, and C-reactive protein during weight maintenanceMichael Miller, Valerie Beach, John D Sorkin, et al.
BMC Nephrology|September 11, 2019
Case report: extreme coronary calcifications and hypomagnesemia in a patient with a 17q12 deletion involving HNF1BHoward J Li, Catherine Groden, Melanie P Hoenig, et al.
Rare (Amsterdam, Netherlands)|March 4, 2024
Calciphylaxis in POEMS syndrome: Case reportDanica Novacic, Thomas Uldrick, Alina Dulau-Florea, et al.
HGG Advances|March 11, 2026
Biallelic Variants in RNU6ATAC Result in a Minor Spliceopathy Characterized by Transcriptome-Wide Minor Intron Retention Events and Short Stature with Variable Multisystem ManifestationsRodrigo Mendez, Taylor M Arriaga, Jialan Ma, et al.
EMBO Molecular Medicine|April 4, 2023
Pathological variants in TOP3A cause distinct disorders of mitochondrial and nuclear genome stabilityDirenis Erdinc, Alejandro Rodríguez-Luis, Mahmoud R Fassad, et al.
American Journal of Human Genetics|July 3, 2018
De Novo Missense Variants in TRAF7 Cause Developmental Delay, Congenital Anomalies, and Dysmorphic FeaturesMari J Tokita, Chun-An Chen, David Chitayat, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.
The New England Journal of Medicine|October 27, 2020
Somatic Mutations in <i>UBA1</i> and Severe Adult-Onset Autoinflammatory DiseaseDavid B Beck, Marcela A Ferrada, Keith A Sikora, et al.
Pageof 1