Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Meena Sivasankaran"'
Publikováno v:
Indian Pediatrics Case Reports, Vol 3, Iss 4, Pp 245-248 (2023)
Background: Eltrombopag and romiplostim are thrombopoietin-receptor agonists (TPO-RA), which are approved globally for the treatment of immune thrombocytopenia. However, thrombopoietin (TPO) is not just a regulator of megakaryocyte expansion but is a
Externí odkaz:
https://doaj.org/article/0ee2435a844b403898f6ad3511ad21cb
Autor:
Niranjan Gurunath Hegde, Meena Sivasankaran, Deenadayalan Munirathnam, G. Vimal Kumar, S. Srinivas
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 4, Pp S38- (2022)
Externí odkaz:
https://doaj.org/article/a8979ca4da094b8d9e1281d0b5b1814c
Autor:
Snehal Shabrish, Madhura Kelkar, Reetika Malik Yadav, Umair Ahmed Bargir, Maya Gupta, Aparna Dalvi, Jahnavi Aluri, Manasi Kulkarni, Shweta Shinde, Sneha Sawant-Desai, Priyanka Kambli, Gouri Hule, Priyanka Setia, Neha Jodhawat, Pallavi Gaikwad, Amruta Dhawale, Nayana Nambiar, Vijaya Gowri, Ambreen Pandrowala, Prasad Taur, Revathi Raj, Ramya Uppuluri, Ratna Sharma, Pranoti Kini, Meena Sivasankaran, Deenadayalan Munirathnam, Ramprasad Vedam, Pandiarajan Vignesh, Aaqib Banday, Amit Rawat, Amita Aggarwal, Ujjal Poddar, Meenakshi Girish, Abhijit Chaudhary, Abhilasha Sampagar, Dharani Jayaraman, Narendra Chaudhary, Nitin Shah, Farah Jijina, S. Chandrakla, Swati Kanakia, Brijesh Arora, Santanu Sen, Madhukar Lokeshwar, Mukesh Desai, Manisha Madkaikar
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of immune dysregulation characterized by hyperactivation of the immune system, excessive cytokine secretion and severe systemic inflammation. HLH is classified as familial (FHL) when associated w
Externí odkaz:
https://doaj.org/article/8417d481a8d94c5c932e6d89d74b864f
Autor:
Pandiarajan Vignesh, Amit Rawat, Rajni Kumrah, Ankita Singh, Anjani Gummadi, Madhubala Sharma, Anit Kaur, Johnson Nameirakpam, Ankur Jindal, Deepti Suri, Anju Gupta, Alka Khadwal, Biman Saikia, Ranjana Walker Minz, Kaushal Sharma, Mukesh Desai, Prasad Taur, Vijaya Gowri, Ambreen Pandrowala, Aparna Dalvi, Neha Jodhawat, Priyanka Kambli, Manisha Rajan Madkaikar, Sagar Bhattad, Stalin Ramprakash, Raghuram CP, Ananthvikas Jayaram, Meena Sivasankaran, Deenadayalan Munirathnam, Sarath Balaji, Aruna Rajendran, Amita Aggarwal, Komal Singh, Fouzia Na, Biju George, Ankit Mehta, Harsha Prasada Lashkari, Ramya Uppuluri, Revathi Raj, Sandip Bartakke, Kirti Gupta, Sreejesh Sreedharanunni, Yumi Ogura, Tamaki Kato, Kohsuke Imai, Koon Wing Chan, Daniel Leung, Osamu Ohara, Shigeaki Nonoyama, Michael Hershfield, Yu-Lung Lau, Surjit Singh
Publikováno v:
Frontiers in Immunology, Vol 11 (2021)
BackgroundSevere Combined Immune Deficiency (SCID) is an inherited defect in lymphocyte development and function that results in life-threatening opportunistic infections in early infancy. Data on SCID from developing countries are scarce.ObjectiveTo
Externí odkaz:
https://doaj.org/article/6fe92a2c434f459ba3dd3d4a3d3c2968
Autor:
Amit Rawat, Pandiarajan Vignesh, Murugan Sudhakar, Madhubala Sharma, Deepti Suri, Ankur Jindal, Anju Gupta, Jitendra Kumar Shandilya, Sathish Kumar Loganathan, Gurjit Kaur, Sanchi Chawla, Pratap Kumar Patra, Alka Khadwal, Biman Saikia, Ranjana Walker Minz, Vaishali Aggarwal, Prasad Taur, Ambreen Pandrowala, Vijaya Gowri, Mukesh Desai, Manasi Kulkarni, Gauri Hule, Umair Bargir, Priyanka Kambli, Manisha Madkaikar, Sagar Bhattad, Chetan Ginigeri, Harish Kumar, Ananthvikas Jayaram, Deenadayalan Munirathnam, Meena Sivasankaran, Revathi Raj, Ramya Uppuluri, Fouzia Na, Biju George, Harsha Prasada Lashkari, Manas Kalra, Anupam Sachdeva, Shishir Seth, Tapas Sabui, Aman Gupta, Karin van Leeuwen, Martin de Boer, Koon Wing Chan, Kohsuke Imai, Osamu Ohara, Shigeaki Nonoyama, Yu Lung Lau, Surjit Singh
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundChronic granulomatous disease (CGD) is an inherited defect in phagocytic respiratory burst that results in severe and life-threatening infections in affected children. Single center studies from India have shown that proportion of autosomal
Externí odkaz:
https://doaj.org/article/22ba47c418d244278fc1f41aa8317b63
Autor:
Priyanka Madhav Kambli, Umair Ahmed Bargir, Reetika Malik Yadav, Maya Ravishankar Gupta, Aparna Dhondi Dalvi, Gouri Hule, Madhura Kelkar, Sneha Sawant-Desai, Priyanka Setia, Neha Jodhawat, Nayana Nambiar, Amruta Dhawale, Pallavi Gaikwad, Shweta Shinde, Prasad Taur, Vijaya Gowri, Ambreen Pandrowala, Anju Gupta, Vibhu Joshi, Madhubala Sharma, Kanika Arora, Rakesh Kumar Pilania, Himanshi Chaudhary, Amita Agarwal, Shobita Katiyar, Sagar Bhattad, Stalin Ramprakash, Raghuram CP, Ananthvikas Jayaram, Vinod Gornale, Revathi Raj, Ramya Uppuluri, Meena Sivasankaran, Deenadayalan Munirathnam, Harsha Prasad Lashkari, Manas Kalra, Anupam Sachdeva, Avinash Sharma, Sarath Balaji, Geeta Madathil Govindraj, Sunil Karande, Ruchi Nanavati, Mamta Manglani, Girish Subramanyam, Abhilasha Sampagar, Indumathi CK, Parinitha Gutha, Swati Kanakia, Shiv Prasad Mundada, Vidya Krishna, Sheela Nampoothiri, Sandeep Nemani, Amit Rawat, Mukesh Desai, Manisha Madkaikar
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Leukocyte adhesion deficiency (LAD) syndrome is a group of inborn errors of immunity characterized by a defect in the cascade of the activation and adhesion leading to the failure of leukocyte to migrate to the site of tissue injury. Three different
Externí odkaz:
https://doaj.org/article/c1e39bcc817b455b9948addad5d93026
Autor:
Meena Sivasankaran, Dhaarani Jayaraman, Shivani Patel, V.S. Venkateswaran, V. Mythili, M. Venkatadesikalu, S. Srinivas, Ramya Uppuluri, Revathi Raj
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 2, p S2 (2017)
Externí odkaz:
https://doaj.org/article/417a303b427c414b91583ca83189dd35
Autor:
Vijaya Gowri, Akshaya Chougule, Maya Gupta, Prasad Taur, Vaishnavi V. Iyengar, Meena Sivasankaran, Deenadayalan Munirathnam, Sushma Krishna, Umair A. Bargir, Aparna Dalvi, Priyanka Setia, Neha Jodhawat, Shweta Shinde, Shakuntala S. Prabhu, Minnie Bodhanwala, Manisha R. Madkaikar, Mukesh M. Desai
Publikováno v:
Scandinavian Journal of Immunology.
Autor:
Srinivas Sankaranarayanan, Dhaarani Jayaraman, Mukul Vij, Deenadayalan Munirathnam, Vimal Kumar, Julius Xavier Scott, Meena Sivasankaran
Publikováno v:
Fetal and pediatric pathology. 41(6)
Background: Primary immunodeficiency (PID) having defects related to lymphocyte cytotoxic pathway or T-cell dysfunction are well known for developing opportunistic infections and Epstein-Barr virus (EBV)-associated diseases. CARMIL2 deficiency is a r
Autor:
Lakshman Vaidhyanathan, Revathi Raj, Nikila Ravichandran, Venkateswaran Vellaichamy Swaminathan, Meena Sivasankaran, Shivani Patel, Indira Jayakumar, Balasubramaniam Ramakrishnan, Ramya Uppuluri, Kesavan Melarcode Ramanan
Publikováno v:
Journal of Clinical Immunology
Haploidentical stem cell transplantation (haplo SCT) has emerged as an acceptable alternative to matched family donor transplantation for children diagnosed to have primary immune deficiency disorders (PIDs). We present data over 4 years on the chall