Items where Author is "Jahnavi, S"
Group by: Item Type | No Grouping Jump to: Article Number of items: 8.
ArticleMohan, V and Radha, V and Nguyen, T T and Stawiski, E W and Pahuja, K B and Goldstein, L D and Tom, Jennifer and Anjana, Ranjit Mohan and Kong-Beltran, Monica and Bhangale, T and Jahnavi, S and Chandni, Radhakrishnan and Gayathri, V and George, P and Zhang, Na and Murugan, Sakthivel and Phalke, Sameer and Chaudhuri, Subhra and Gupta, Ravi and Zhang, Jingli and Santhosh, Sam and Stinson, Jeremy and Modrusan, Zora and Ramprasad, V. L. and Seshagiri, Somasekar and Peterson, Andrew S. (2018) Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India. BMC Medical Genetics, 19 (1). ISSN 1471-2350 Jahnavi, S and Poovazhagi, V and Kanthimathi, S and Gayathri, V and Mohan, V and Radha, V (2014) EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndrome. Pediatric diabetes, 15 (4). pp. 313-8. ISSN 1399-5448 Kanthimathi, S and Jahnavi, S and Balamurugan, K and Ranjani, H and Sonya, J and Goswami, S and Chowdhury, S and Mohan, V and Radha, V (2014) Glucokinase Gene Mutations (MODY 2) in Asian Indians. Diabetes Technology & Therapeutics, 16 (3). p. 180. ISSN 1520-9156 Jahnavi, S and Poovazhagi, V and Kanthimathi, S and Balamurugan, K and Bodhini, D and Yadav, J and Jain, V and Khadgawat, R and Sikdar, M and Bhavatharini, A and Das, A K and Kaur, T and Mohan, V and Radha, V (2014) NovelABCC8(SUR1) Gene Mutations in Asian Indian Children with Congenital Hyperinsulinemic Hypoglycemia. Annals of Human Genetics, 78 (5). p. 311. ISSN 00034800 Poovazhagi, V and Shanthirani, S and Jahnavi, S and Radha, V and Mohan, V (2013) Berardinelli Seip congenital lipodystrophy presenting with neonatal diabetes mellitus due to a mutation in the AGPAT2 gene. International Journal of Diabetes in Developing Countries, 33 (1). p. 66. ISSN 0973-3930 Jahnavi, S and Poovazhagi, V and Mohan, V and Bodhini, D and Raghupathy, P and Amutha, A and Suresh Kumar, P and Adhikari, P and Shriraam, M and Kaur, T and Das, A K and Molnes, J and Njolstad, P R and Unnikrishnan, R and Radha, V (2013) Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children. Clinical genetics, 83 (5). pp. 439-45. ISSN 1399-0004 Poovazhagi, V and Sangaralingam, T and Senniappan, S and Jahnavi, S and Radha, V and Mohan, V (2013) Clinical Presentation and Long Term Outcome of 40 children with Infantile Onset Diabetes Mellitus in South India. Indian pediatrics . ISSN 0974-7559 Atray, A and Jahnavi, S and Thai, K and Hiremath, P and Anjana, R M and Unnikrishnan, R and Mohan, V and Radha, V (2013) Rabson Mendenhall Syndrome; a case report. Journal of Diabetology, 2 (4). pp. 1-5. |