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  1. 1
    Profile of pediatric vasculitides – Prospective hospital-based data from eastern India

    Profile of pediatric vasculitides – Prospective hospital-based data from eastern India by Arpan Saha, Sumantra Sarkar, Tanushree Mondal

    Published 2021-01-01
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  2. 2
    Rare and novel variant load threshold for KIF7, GJA1 and PDE1C genes elevates the risk of severity of congenital heart defects in Down syndrome

    Rare and novel variant load threshold for KIF7, GJA1 and PDE1C genes elevates the risk of severity of congenital heart defects in Down syndrome by Agnish Ganguly, Samudra Pal, Srilagna Chatterjee, Madhusudan Das, Sumantra Sarkar, Sujay Ghosh

    Published 2025-01-01
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  3. 3
    Health-related quality of life in children with juvenile idiopathic arthritis: A developing country perspective

    Health-related quality of life in children with juvenile idiopathic arthritis: A developing country perspective by Madhumita Nandi, Abhisek Majhi, Moumita Samanta, Tanmoy Sar, Sumantra Sarkar, Tapas Sabui

    Published 2022-01-01
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  4. 4
    Rare and novel variant load threshold for KIF7, GJA1 and PDE1C genes elevates the risk of severity of congenital heart defects in Down syndrome.

    Rare and novel variant load threshold for KIF7, GJA1 and PDE1C genes elevates the risk of severity of congenital heart defects in Down syndrome. by Agnish Ganguly, Samudra Pal, Srilagna Chatterjee, Madhusudan Das, Sumantra Sarkar, Sujay Ghosh

    Published 2025-01-01
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  5. 5
    Status of Vitamin D in Childhood-onset Systemic Lupus Erythematosus and its Relation with the Disease Activity

    Status of Vitamin D in Childhood-onset Systemic Lupus Erythematosus and its Relation with the Disease Activity by Dikpati Mukherjee, Sumantra Sarkar, Suprit Basu, Supratim Datta, Madhumita Nandi, Paramita Das

    Published 2025-07-01
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  6. 6
    The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte.

    The etiology of Down syndrome: Maternal MCM9 polymorphisms increase risk of reduced recombination and nondisjunction of chromosome 21 during meiosis I within oocyte. by Upamanyu Pal, Pinku Halder, Anirban Ray, Sumantra Sarkar, Supratim Datta, Papiya Ghosh, Sujay Ghosh

    Published 2021-03-01
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