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Neerja Gupta

Showing results (91-100 of 237) with videos related to

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Neurology India|September 11, 2021
Cerebral Venous Sinus Thrombosis in a Child with Lesch-Nyhan SyndromeRanjith K Manokaran, Prashant Jauhari, Biswaroop Chakrabarty, et al.
Clinical Dysmorphology|January 24, 2019
Apert syndrome with congenital diaphragmatic hernia: another case report and review of the literatureRavneet Kaur, Puneeta Mishra, Surjeet Kumar, et al.
Clinical and Experimental Nephrology|May 27, 2008
Mutations in OCRL1 gene in Indian children with Lowe syndromeSidharth Kumar Sethi, Arvind Bagga, Ashima Gulati, et al.
The Indian Journal of Radiology & Imaging|March 29, 2024
Hand Radiographs in Skeletal Dysplasia: A Pictorial ReviewDheeksha D S, Stuti Chandola, Aayush Jain, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett SyndromeRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Journal of Child Neurology|February 15, 2017
Validation of Polymerase Chain Reaction-Based Assay to Detect Actual Number of CGG Repeats in FMR1 Gene in Indian Fragile X Syndrome PatientsMadhumita Roy Chowdhury, Sandeepa Chauhan, Anjali Dabral, et al.
Journal of Pediatric Neurosciences|June 4, 2014
Menkes disease - An important cause of early onset refractory seizuresPuneet Jain, Lakshminarayanan Kannan, Biswaroop Chakrabarty, et al.
Indian Journal of Pediatrics|April 19, 2024
Hematopoietic Stem Cell Transplantation for Storage Disorders: Present StatusSoumalya Chakraborty, Aditya Kumar Gupta, Neerja Gupta, et al.
Brain & Development|February 9, 2011
Novel non-identical MECP2 mutations in Rett syndrome family: a rare presentationRajni Khajuria, Neerja Gupta, Savita Sapra, et al.
Journal of Child Neurology|February 3, 2011
A novel MECP2 change in an indian boy with variant rett phenotype and congenital blindness: implications for genetic counseling and prenatal diagnosisRajni Khajuria, Neerja Gupta, Savita Sapra, et al.
Pageof 24

Showing results (91-100 of 237) with videos related to

Sort By:
Pageof 24
Neurology India|September 11, 2021
Cerebral Venous Sinus Thrombosis in a Child with Lesch-Nyhan SyndromeRanjith K Manokaran, Prashant Jauhari, Biswaroop Chakrabarty, et al.
Clinical Dysmorphology|January 24, 2019
Apert syndrome with congenital diaphragmatic hernia: another case report and review of the literatureRavneet Kaur, Puneeta Mishra, Surjeet Kumar, et al.
Clinical and Experimental Nephrology|May 27, 2008
Mutations in OCRL1 gene in Indian children with Lowe syndromeSidharth Kumar Sethi, Arvind Bagga, Ashima Gulati, et al.
The Indian Journal of Radiology & Imaging|March 29, 2024
Hand Radiographs in Skeletal Dysplasia: A Pictorial ReviewDheeksha D S, Stuti Chandola, Aayush Jain, et al.
Human Genetics|January 29, 2010
Novel human pathological mutations. Gene symbol: MECP2. Disease: Rett SyndromeRajni Khajuria, Savita Sapra, Manju Ghosh, et al.
Journal of Child Neurology|February 15, 2017
Validation of Polymerase Chain Reaction-Based Assay to Detect Actual Number of CGG Repeats in FMR1 Gene in Indian Fragile X Syndrome PatientsMadhumita Roy Chowdhury, Sandeepa Chauhan, Anjali Dabral, et al.
Journal of Pediatric Neurosciences|June 4, 2014
Menkes disease - An important cause of early onset refractory seizuresPuneet Jain, Lakshminarayanan Kannan, Biswaroop Chakrabarty, et al.
Indian Journal of Pediatrics|April 19, 2024
Hematopoietic Stem Cell Transplantation for Storage Disorders: Present StatusSoumalya Chakraborty, Aditya Kumar Gupta, Neerja Gupta, et al.
Brain & Development|February 9, 2011
Novel non-identical MECP2 mutations in Rett syndrome family: a rare presentationRajni Khajuria, Neerja Gupta, Savita Sapra, et al.
Journal of Child Neurology|February 3, 2011
A novel MECP2 change in an indian boy with variant rett phenotype and congenital blindness: implications for genetic counseling and prenatal diagnosisRajni Khajuria, Neerja Gupta, Savita Sapra, et al.
Pageof 24