Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Prasad Taur"'
Autor:
Akshaya Chougule, Prasad Taur, Vaishnavi V. Iyengar, Vijaya Gowri, Bipin P. Kulkarni, Manisha R. Madkaikar, Minnie Bodhanwala, Mukesh M. Desai
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 8, Iss 1, Pp 4-9 (2023)
Leukocyte adhesion deficiency (LAD) Type-III is caused by homozygous mutations in FERMT3 causing Kindlin-3 deficiency. Here we describe three children with molecularly proven LAD-III presenting with neonatal onset mucocutaneous bleeding, infections a
Externí odkaz:
https://doaj.org/article/09e0c1d7cc2e45dd9b9b317efe3b63a1
Autor:
Madhu Chhanda Mohanty, Mukesh Desai, Ahmad Mohammad, Amita Aggarwal, Geeta Govindaraj, Sagar Bhattad, Harsha Prasada Lashkari, Liza Rajasekhar, Harish Verma, Arun Kumar, Unnati Sawant, Swapnil Yashwant Varose, Prasad Taur, Reetika Malik Yadav, Manogat Tatkare, Mevis Fernandes, Umair Bargir, Sanjukta Majumdar, Athulya Edavazhippurath, Jyoti Rangarajan, Ramesh Manthri, Manisha Ranjan Madkaikar
Publikováno v:
Vaccines, Vol 11, Iss 7, p 1211 (2023)
The emergence of vaccine-derived polioviruses (VDPVs) in patients with Primary Immunodeficiency (PID) is a threat to the polio-eradication program. In a first of its kind pilot study for successful screening and identification of VDPV excretion among
Externí odkaz:
https://doaj.org/article/9e7015778aa347ddb270543ed528e298
Autor:
Deepti Suri, Rashmi Rikhi, Ankur K. Jindal, Amit Rawat, Murugan Sudhakar, Pandiarajan Vignesh, Anju Gupta, Anit Kaur, Jyoti Sharma, Jasmina Ahluwalia, Prateek Bhatia, Alka Khadwal, Revathi Raj, Ramya Uppuluri, Mukesh Desai, Prasad Taur, Ambreen A. Pandrowala, Vijaya Gowri, Manisha R. Madkaikar, Harsha Prasada Lashkari, Sagar Bhattad, Harish Kumar, Sanjeev Verma, Kohsuke Imai, Shigeaki Nonoyama, Osamu Ohara, Koon W. Chan, Pamela P. Lee, Yu Lung Lau, Surjit Singh
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
BackgroundWiskott Aldrich syndrome (WAS) is characterized by bleeding manifestations, recurrent infections, eczema, autoimmunity, and malignancy. Over the last decade, improved awareness and better in-house diagnostic facilities at several centers in
Externí odkaz:
https://doaj.org/article/40f9e91155324dac9955f31d9057e303
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:
Deepti Suri, Amit Rawat, Ankur Kumar Jindal, Pandiarajan Vignesh, Anju Gupta, Rakesh Kumar Pilania, Vibhu Joshi, Kanika Arora, Rajni Kumrah, Gummadi Anjani, Amita Aggarwal, Shubha Phadke, Fouzia N. Aboobacker, Biju George, Eunice Sindhuvi Edison, Mukesh Desai, Prasad Taur, Vijaya Gowri, Ambreen Abdulwahab Pandrowala, Sagar Bhattad, Swati Kanakia, Marco Gottorno, Isabella Ceccherini, Adriana Almeida de Jesus, Raphaela Goldbach-Mansky, Michael S. Hershfield, Surjit Singh
Publikováno v:
Frontiers in Immunology, Vol 12 (2021)
Background: Systemic autoinflammatory diseases (SAID) are rare inherited disorders involving genes regulating innate immune signaling and are characterized by periodic or chronic multi-systemic inflammation.Objective: To describe spectrum of clinical
Externí odkaz:
https://doaj.org/article/a93420f803dd40d082f9ff6cd12c0cbc
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:
Amit Rawat, Ankur Kumar Jindal, Deepti Suri, Pandiarajan Vignesh, Anju Gupta, Biman Saikia, Ranjana W. Minz, Aaqib Zaffar Banday, Rahul Tyagi, Kanika Arora, Vibhu Joshi, Sanjib Mondal, Jitendra Kumar Shandilya, Madhubala Sharma, Mukesh Desai, Prasad Taur, Ambreen Pandrowala, Vijaya Gowri, Sneha Sawant-Desai, Maya Gupta, Aparna Dhondi Dalvi, Manisha Madkaikar, Amita Aggarwal, Revathi Raj, Ramya Uppuluri, Sagar Bhattad, Ananthvikas Jayaram, Harsha Prasad Lashkari, Liza Rajasekhar, Deenadayalan Munirathnam, Manas Kalra, Anuj Shukla, Ruchi Saka, Rajni Sharma, Ravinder Garg, Kohsuke Imai, Shigeaki Nonoyama, Osamu Ohara, Pamela P. Lee, Koon Wing Chan, Yu-Lung Lau, Surjit Singh
Publikováno v:
Frontiers in Immunology, Vol 11 (2021)
BackgroundThere is paucity of literature on XLA from developing countries. Herein we report the clinical and molecular profile and outcome in a multicenter cohort of patients with XLA from India.MethodsData on XLA from all regional centers supported
Externí odkaz:
https://doaj.org/article/d6072f7834b5437f86ee0d2b861f852d
Autor:
Reetika Malik Yadav, Maya Gupta, Aparna Dalvi, Umair Ahmed Bargir, Gouri Hule, Snehal Shabrish, Jahnavi Aluri, Manasi Kulkarni, Priyanka Kambli, Ramya Uppuluri, Suresh Seshadri, Sujatha Jagadeesh, Beena Suresh, Jayarekha Raja, Prasad Taur, Sivasankar Malaischamy, Priyanka Ghosh, Shweta Mahalingam, Priya Kadam, Harsha Prasada Lashkari, Parag Tamhankar, Vasundhara Tamhankar, Shilpa Mithbawkar, Sagar Bhattad, Prerna Jhawar, Adinarayan Makam, Vandana Bansal, Malathi Prasad, Geeta Govindaraj, Beena Guhan, Karthik Bharadwaj Tallapaka, Mukesh Desai, Revathi Raj, Manisha Rajan Madkaikar
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Prenatal Diagnosis (PND) forms an important part of primary preventive management for families having a child affected with primary immunodeficiency. Although individually sparse, collectively this group of genetic disorders represents a significant
Externí odkaz:
https://doaj.org/article/6a8ad79b624d4b21a0987ecfc475eba9
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