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Mamta Muranjan

Showing results (1-10 of 47) with videos related to

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Molecular Cytogenetics|June 24, 2014
Enzyme replacement therapy for lysosomal storage disorders in IndiaMamta Muranjan
Indian Journal of Pediatrics|April 26, 2014
The unforeseen toll of birth defects and their economic burden at a tertiary care public institute in MumbaiMamta Muranjan, P Vijayalakshmi
Indian Pediatrics|July 11, 2016
Outcome of Gaucher Disease in India: Lessons from Prevalent Diagnostic and Therapeutic PracticesMamta Muranjan, Smita Patil
Journal of Pediatric Genetics|December 1, 2021
Diagnosis is in the Eye of the Beholder: Barriers to Early Diagnosis of Mucopolysaccharidosis in Children in IndiaMeenu Grewal, Mamta Muranjan
The Pediatric Infectious Disease Journal|October 19, 2016
Acute Paraparesis Due to Lumbosacral Radiculopathy With Concomitant Meningitis: Unusual Presentation of Scrub TyphusMamta Muranjan, Sunil Karande
Indian Pediatrics|July 2, 2011
An observational, health service based survey for missed opportunities for immunizationMamta Muranjan, Chhaya Mehta, Abhijit Pakhare
BMJ Case Reports|November 25, 2015
Muddy clinical waters: a missed betel nut in the bronchusSunil Karande, Pradeep Vaideeswar, Mamta Muranjan
The National Medical Journal of India|August 24, 2023
Economic burden of beta-thalassaemia major receiving hypertransfusion therapy at a public hospital in MumbaiAshwija Uchil, Mamta Muranjan, Nithya J Gogtay
Indian Pediatrics|August 13, 2009
Phenotypic heterogeneity and parental origin of extra chromosome 21 in Down syndromeMamta Muranjan, Tejasvi Chaudhari, Babu Rao Vundinti
Indian Journal of Pediatrics|July 7, 2015
Erratum to: The Face of Lysosomal Storage Disorders in India: A Need for Early DiagnosisShruti Agarwal, Keya Lahiri, Mamta Muranjan, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Molecular Cytogenetics|June 24, 2014
Enzyme replacement therapy for lysosomal storage disorders in IndiaMamta Muranjan
Indian Journal of Pediatrics|April 26, 2014
The unforeseen toll of birth defects and their economic burden at a tertiary care public institute in MumbaiMamta Muranjan, P Vijayalakshmi
Indian Pediatrics|July 11, 2016
Outcome of Gaucher Disease in India: Lessons from Prevalent Diagnostic and Therapeutic PracticesMamta Muranjan, Smita Patil
Journal of Pediatric Genetics|December 1, 2021
Diagnosis is in the Eye of the Beholder: Barriers to Early Diagnosis of Mucopolysaccharidosis in Children in IndiaMeenu Grewal, Mamta Muranjan
The Pediatric Infectious Disease Journal|October 19, 2016
Acute Paraparesis Due to Lumbosacral Radiculopathy With Concomitant Meningitis: Unusual Presentation of Scrub TyphusMamta Muranjan, Sunil Karande
Indian Pediatrics|July 2, 2011
An observational, health service based survey for missed opportunities for immunizationMamta Muranjan, Chhaya Mehta, Abhijit Pakhare
BMJ Case Reports|November 25, 2015
Muddy clinical waters: a missed betel nut in the bronchusSunil Karande, Pradeep Vaideeswar, Mamta Muranjan
The National Medical Journal of India|August 24, 2023
Economic burden of beta-thalassaemia major receiving hypertransfusion therapy at a public hospital in MumbaiAshwija Uchil, Mamta Muranjan, Nithya J Gogtay
Indian Pediatrics|August 13, 2009
Phenotypic heterogeneity and parental origin of extra chromosome 21 in Down syndromeMamta Muranjan, Tejasvi Chaudhari, Babu Rao Vundinti
Indian Journal of Pediatrics|July 7, 2015
Erratum to: The Face of Lysosomal Storage Disorders in India: A Need for Early DiagnosisShruti Agarwal, Keya Lahiri, Mamta Muranjan, et al.
Pageof 5