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

Kalpana Gowrishankar

Showing results (1-10 of 30) with videos related to

Pageof 3
Sort By:
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 28, 2021
Lethal Restrictive Dermopathy with <i>ZMPSTE24</i> MutationImmanuel Pradeep, Kalpana Gowrishankar, Lakshmi Shanmugasundaram
Indian Journal of Orthopaedics|May 28, 2015
Genetic disorders with heterotopic ossificansRuthiramurthy Sankar, Kalpana Gowrishankar, Saraswati Viswanathan
Indian Journal of Pediatrics|July 1, 2004
Fibrodysplasia ossificans progressivaL Subramanyam, Kalpana Gowrishankar, So Shivbalan, et al.
Journal of Genetics|October 6, 2020
A <i>de novo</i> marker chromosome 15 in a child with isolated developmental delayMadhavan Jeevan Kumar, Kalpana Gowrishankar, Venkatasubramanian Hemagowri, et al.
Indian Journal of Pediatrics|April 7, 2009
Thiamine responsive megaloblastic anemia syndromeRamaswamy Ganesh, S Ezhilarasi, Thiruvengadam Vasanthi, et al.
Indian Journal of Pediatrics|May 9, 2014
Profile of hemophagocytic lymphohistiocytosis; efficacy of intravenous immunoglobulin therapySarala Rajajee, Indhumathi Ashok, Nitin Manwani, et al.
Indian Journal of Human Genetics|February 21, 2012
Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic associationJeevan M Kumar, Kalpana Gowrishankar, T Vasanthi, et al.
Genetic Testing and Molecular Biomarkers|July 9, 2015
Association of ACE and MDR1 Gene Polymorphisms with Steroid Resistance in Children with Idiopathic Nephrotic SyndromeMohanapriya Chinambedu Dhandapani, Vettriselvi Venkatesan, Nammalwar Bollam Rengaswamy, et al.
Clinical and Experimental Nephrology|January 29, 2016
Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian childrenMohanapriya Chinambedu Dhandapani, Vettriselvi Venkatesan, Nammalwar Bollam Rengaswamy, et al.
Journal of Cellular Biochemistry|September 2, 2018
Novel variations in NPHS1 gene in children of South Indian population and its association with primary nephrotic syndromeChinambedu Dhandapani Mohanapriya, Venkatesan Vettriselvi, Bollam Rengaswamy Nammalwar, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 28, 2021
Lethal Restrictive Dermopathy with <i>ZMPSTE24</i> MutationImmanuel Pradeep, Kalpana Gowrishankar, Lakshmi Shanmugasundaram
Indian Journal of Orthopaedics|May 28, 2015
Genetic disorders with heterotopic ossificansRuthiramurthy Sankar, Kalpana Gowrishankar, Saraswati Viswanathan
Indian Journal of Pediatrics|July 1, 2004
Fibrodysplasia ossificans progressivaL Subramanyam, Kalpana Gowrishankar, So Shivbalan, et al.
Journal of Genetics|October 6, 2020
A <i>de novo</i> marker chromosome 15 in a child with isolated developmental delayMadhavan Jeevan Kumar, Kalpana Gowrishankar, Venkatasubramanian Hemagowri, et al.
Indian Journal of Pediatrics|April 7, 2009
Thiamine responsive megaloblastic anemia syndromeRamaswamy Ganesh, S Ezhilarasi, Thiruvengadam Vasanthi, et al.
Indian Journal of Pediatrics|May 9, 2014
Profile of hemophagocytic lymphohistiocytosis; efficacy of intravenous immunoglobulin therapySarala Rajajee, Indhumathi Ashok, Nitin Manwani, et al.
Indian Journal of Human Genetics|February 21, 2012
Isochromosome X mosaicism in a child with Kabuki syndrome phenotype: A rare cytogenetic associationJeevan M Kumar, Kalpana Gowrishankar, T Vasanthi, et al.
Genetic Testing and Molecular Biomarkers|July 9, 2015
Association of ACE and MDR1 Gene Polymorphisms with Steroid Resistance in Children with Idiopathic Nephrotic SyndromeMohanapriya Chinambedu Dhandapani, Vettriselvi Venkatesan, Nammalwar Bollam Rengaswamy, et al.
Clinical and Experimental Nephrology|January 29, 2016
Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian childrenMohanapriya Chinambedu Dhandapani, Vettriselvi Venkatesan, Nammalwar Bollam Rengaswamy, et al.
Journal of Cellular Biochemistry|September 2, 2018
Novel variations in NPHS1 gene in children of South Indian population and its association with primary nephrotic syndromeChinambedu Dhandapani Mohanapriya, Venkatesan Vettriselvi, Bollam Rengaswamy Nammalwar, et al.
Pageof 3