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Sumita Danda

Showing results (31-40 of 155) with videos related to

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Clinical Dysmorphology|July 6, 2016
De Barsy syndrome type B presenting with cardiac and genitourinary abnormalitiesAtanu K Dutta, Alka V Ekbote, Niranjan Thomas, et al.
Clinical Kidney Journal|April 9, 2015
Renal manifestations of tuberous sclerosis among children: an Indian experience and review of the literatureSophy Korula, Alka Ekbote, Naresh Kumar, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 22, 2021
Meconium Ileus due to GUCY2C gene mutations in three unrelated South Indian familiesSneha Varkki, Antony Terance Benjamin, Rekha Athiyarath, et al.
Indian Journal of Community Medicine : Official Publication of Indian Association of Preventive & Social Medicine|February 24, 2021
Prevalence of Vitamin B12 Deficiency and Its Associated Risk Factors among Pregnant Women of Rural South India: A Community-based Cross-sectional StudyAnitha Mohanraj Barney, Vinod Joseph Abraham, Sumita Danda, et al.
Annals of Indian Academy of Neurology|December 23, 2022
Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic DisorderSophy Korula, Sangeetha Yoganathan, Jeyanthi Peter, et al.
Seminars in Arthritis and Rheumatism|December 29, 2012
A descriptive analysis of 14 cases of progressive-psuedorheumatoid-arthropathy of childhood from south India: review of literature in comparison with juvenile idiopathic arthritisAlka V Ekbote, Debashish Danda, Sathish Kumar, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 19, 2014
Patient with mutation in the matrix metalloproteinase 2 (MMP2) gene - a case report and review of the literatureAlka V Ekbote, Sumita Danda, Andreas Zankl, et al.
Iranian Journal of Child Neurology|April 27, 2018
Novel Imaging Finding and Novel Mutation in an Infant with Molybdenum Cofactor Deficiency, a Mimicker of Hypoxic-Ischaemic EncephalopathySangeetha Yoganathan, SniyaVALSA Sudhakar, Maya Thomas, et al.
Journal of Tropical Pediatrics|September 17, 2009
Development and dysmorphism in Joubert syndrome--short case series from IndiaBeena Koshy, Samuel Philip Oommen, Smitha Jasper, et al.
Neuropediatrics|February 10, 2016
Beta Propellar Protein-Associated Neurodegeneration: A Rare Cause of Infantile Autistic Regression and Intracranial CalcificationSangeetha Yoganathan, Gautham Arunachal, Sniya Valsa Sudhakar, et al.
Pageof 16

Showing results (31-40 of 155) with videos related to

Sort By:
Pageof 16
Clinical Dysmorphology|July 6, 2016
De Barsy syndrome type B presenting with cardiac and genitourinary abnormalitiesAtanu K Dutta, Alka V Ekbote, Niranjan Thomas, et al.
Clinical Kidney Journal|April 9, 2015
Renal manifestations of tuberous sclerosis among children: an Indian experience and review of the literatureSophy Korula, Alka Ekbote, Naresh Kumar, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 22, 2021
Meconium Ileus due to GUCY2C gene mutations in three unrelated South Indian familiesSneha Varkki, Antony Terance Benjamin, Rekha Athiyarath, et al.
Indian Journal of Community Medicine : Official Publication of Indian Association of Preventive & Social Medicine|February 24, 2021
Prevalence of Vitamin B12 Deficiency and Its Associated Risk Factors among Pregnant Women of Rural South India: A Community-based Cross-sectional StudyAnitha Mohanraj Barney, Vinod Joseph Abraham, Sumita Danda, et al.
Annals of Indian Academy of Neurology|December 23, 2022
Late Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Rare Treatable Neurometabolic DisorderSophy Korula, Sangeetha Yoganathan, Jeyanthi Peter, et al.
Seminars in Arthritis and Rheumatism|December 29, 2012
A descriptive analysis of 14 cases of progressive-psuedorheumatoid-arthropathy of childhood from south India: review of literature in comparison with juvenile idiopathic arthritisAlka V Ekbote, Debashish Danda, Sathish Kumar, et al.
Journal of Clinical Research in Pediatric Endocrinology|March 19, 2014
Patient with mutation in the matrix metalloproteinase 2 (MMP2) gene - a case report and review of the literatureAlka V Ekbote, Sumita Danda, Andreas Zankl, et al.
Iranian Journal of Child Neurology|April 27, 2018
Novel Imaging Finding and Novel Mutation in an Infant with Molybdenum Cofactor Deficiency, a Mimicker of Hypoxic-Ischaemic EncephalopathySangeetha Yoganathan, SniyaVALSA Sudhakar, Maya Thomas, et al.
Journal of Tropical Pediatrics|September 17, 2009
Development and dysmorphism in Joubert syndrome--short case series from IndiaBeena Koshy, Samuel Philip Oommen, Smitha Jasper, et al.
Neuropediatrics|February 10, 2016
Beta Propellar Protein-Associated Neurodegeneration: A Rare Cause of Infantile Autistic Regression and Intracranial CalcificationSangeetha Yoganathan, Gautham Arunachal, Sniya Valsa Sudhakar, et al.
Pageof 16