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

S Danda

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
The West Indian Medical Journal|November 1, 2013
Tel Hashomer camptodactyly syndrome: a case reportK Shah, R Sreekanth, B Thomas, et al.
Indian Pediatrics|February 15, 2001
Juvenile Sandhoff diseaseA G Unnikrishnan, S Danda, M S Seshadri
Indian Pediatrics|August 26, 1998
Acromesomelic dwarfism: report of a family with two affected siblingsS Danda, S R Phadke, S S Agarwal
Nephrology (Carlton, Vic.)|March 5, 2004
High-dose iron gluconate in chronic kidney disease patientsRatna S Danda, Linda J Kirk, Pablo E Pergola
Indian Journal of Human Genetics|September 30, 2011
Camptodactyly in Sotos syndromeS Danda, M C Mathew, S M Bain, et al.
Lupus|February 17, 2010
Klinefelter syndrome with systemic lupus erythematosus in an Indian manA Bertha, S Danda, E Tjandrajana, et al.
Indian Pediatrics|February 27, 2001
Chromosomes 6/7 translocation t(6:7)(q15;32) presenting as multiple pterygium syndromeV Madhuri, A Bose, S Danda, et al.
The Indian Journal of Medical Research|December 31, 2020
Authors' responseS Danda, B M Thomas, G Paramshivam, et al.
Indian Journal of Nephrology|August 12, 2016
Recurrent truncating mutations in alanine-glyoxylate aminotransferase gene in two South Indian families with primary hyperoxaluria type 1 causing later onset end-stage kidney diseaseA K Dutta, B K Paulose, S Danda, et al.
American Journal of Physiology. Renal Physiology|February 11, 2005
EGF stimulates mesangial cell mitogenesis via PI3-kinase-mediated MAPK-dependent and AKT kinase-independent manner: involvement of c-fos and p27Kip1Lenin Mahimainathan, Nandini Ghosh-Choudhury, Balachandar A Venkatesan, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
The West Indian Medical Journal|November 1, 2013
Tel Hashomer camptodactyly syndrome: a case reportK Shah, R Sreekanth, B Thomas, et al.
Indian Pediatrics|February 15, 2001
Juvenile Sandhoff diseaseA G Unnikrishnan, S Danda, M S Seshadri
Indian Pediatrics|August 26, 1998
Acromesomelic dwarfism: report of a family with two affected siblingsS Danda, S R Phadke, S S Agarwal
Nephrology (Carlton, Vic.)|March 5, 2004
High-dose iron gluconate in chronic kidney disease patientsRatna S Danda, Linda J Kirk, Pablo E Pergola
Indian Journal of Human Genetics|September 30, 2011
Camptodactyly in Sotos syndromeS Danda, M C Mathew, S M Bain, et al.
Lupus|February 17, 2010
Klinefelter syndrome with systemic lupus erythematosus in an Indian manA Bertha, S Danda, E Tjandrajana, et al.
Indian Pediatrics|February 27, 2001
Chromosomes 6/7 translocation t(6:7)(q15;32) presenting as multiple pterygium syndromeV Madhuri, A Bose, S Danda, et al.
The Indian Journal of Medical Research|December 31, 2020
Authors' responseS Danda, B M Thomas, G Paramshivam, et al.
Indian Journal of Nephrology|August 12, 2016
Recurrent truncating mutations in alanine-glyoxylate aminotransferase gene in two South Indian families with primary hyperoxaluria type 1 causing later onset end-stage kidney diseaseA K Dutta, B K Paulose, S Danda, et al.
American Journal of Physiology. Renal Physiology|February 11, 2005
EGF stimulates mesangial cell mitogenesis via PI3-kinase-mediated MAPK-dependent and AKT kinase-independent manner: involvement of c-fos and p27Kip1Lenin Mahimainathan, Nandini Ghosh-Choudhury, Balachandar A Venkatesan, et al.
Pageof 2