Mamta Muranjan

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 9

Top Topics

Replacement Therapy

Health Insurance

Top Venues

BMJ case reports

Journal of pediatric genetics

Indian journal of pediatrics

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

Publications

Shweta Mhatre, Mamta Muranjan, Sunil Karande, Aparna Thirumalaiswamy
Deficiency of adenosine deaminase 2: a genetic autoinflammatory disorder mimicking childhood polyarteritis nodosa. BMJ case reports 17 (5) (2024)
Shweta Mhatre, Mamta Muranjan, Sunil Karande, Aparna Thirumalaiswamy
Deficiency of adenosine deaminase 2: a genetic autoinflammatory disorder mimicking childhood polyarteritis nodosa. BMJ case reports 17 (5) (2024)
Shweta Mhatre, Mamta Muranjan, Sunil Karande, Aparna Thirumalaiswamy
Deficiency of adenosine deaminase 2: a genetic autoinflammatory disorder mimicking childhood polyarteritis nodosa. BMJ case reports 17 (5) (2024)
Shweta Mhatre, Mamta Muranjan, Sunil Karande, Aparna Thirumalaiswamy
Deficiency of adenosine deaminase 2: a genetic autoinflammatory disorder mimicking childhood polyarteritis nodosa. BMJ case reports 17 (5) (2024)
Shweta P Mhatre, Mamta Muranjan, Nithya J Gogtay
Economic Burden of Gaucher Disease at a Tertiary Care Public Hospital in Mumbai. Indian journal of pediatrics (2023)
Shweta Mhatre, Mamta Muranjan, Sunil Karande, Harish Balaji
Novel manifestations of Farber disease mimicking neuronopathic Gaucher disease. BMJ case reports 14 (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)
Meenu Grewal, Mamta Muranjan
Diagnosis is in the Eye of the Beholder: Barriers to Early Diagnosis of Mucopolysaccharidosis in Children in India. Journal of pediatric genetics 10 (4) (2020)
Parag M Tamhankar, Lakshmi Vasudevan, Pratima Kondurkar, Sarfaraj Niazi, Rita Christopher, Dhaval Solanki, Pooja Dholakia, Mamta Muranjan, Mahesh Kamate, Umesh Kalane, Jayesh Sheth, Vasundhara Tamhankar, Reena Gulati, Madhavi Vasikarla, Sumita Danda, Shaik M Naushad, Katta M Girisha, Shekhar Patil
Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1. Journal of pediatric genetics 10 (3) (2020)