Radharamadevi Akella (Akella Radha Rama Devi, Radha Rama Devi A)

Publication Activity (10 Years)

Years Active: 2021-2022
Publications (10 Years): 4

Top Topics

Intellectual Disability

Hepatitis C Virus

Top Venues

Journal of pediatric genetics

Clinical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Radharamadevi Akella
SWI/SNF-Related SMARCA2 Gene Mutation Associated with Nicolaides-Baraitser's Syndrome: Follow-up Study. Journal of pediatric genetics 13 (2) (2022)
Radharamadevi Akella
SWI/SNF-Related SMARCA2 Gene Mutation Associated with Nicolaides-Baraitser's Syndrome: Follow-up Study. Journal of pediatric genetics 13 (2) (2022)
Radharamadevi Akella, Shaik Mohammad Naushad, Romit Jain, Lokesh Lingappa
A rare case of fatty acyl-CoA reductase 1 deficiency in an Indian infant manifesting rhizomelic chondrodystrophy phenotype. Clinical genetics 99 (5) (2021)
Dipti Deshpande, Shailesh Kumar Gupta, Asodu Sandeep Sarma, Prajnya Ranganath, Jamal Md Nurul Jain S, Jayesh Sheth, Mehul Mistri, Neerja Gupta, Madhulika Kabra, Shubha R Phadke, Katta M Girisha, Ratna Dua Puri, Shagun Aggarwal, Chaitanya Datar, Kausik Mandal, Preetha Tilak, Mamta Muranjan, Sunita Bijarnia-Mahay, Radharamadevi Akella, Naresh B Tayade, Akash Ranjan, Ashwin B Dalal
Functional characterization of novel variants in SMPD1 in Indian patients with acid sphingomyelinase deficiency. Human mutation 42 (10) (2021)