Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Jitendra Kumar Shandilya"'
Autor:
Pandiarajan Vignesh, Amit Rawat, Jitendra Kumar Shandilya, Man Updesh Singh Sachdeva, Jasmina Ahluwalia, Surjit Singh
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-7 (2021)
Abstract Background Platelet activation is an integral part of pathogenesis of Kawasaki disease (KD). However, there is paucity of literature on flow-cytometry based assessment of platelet activation in KD. We aimed to analyse monocyte-platelet aggre
Externí odkaz:
https://doaj.org/article/5beead116bce46c380c3927e73569d10
Autor:
Gummadi Anjani, Pandiarajan Vignesh, Vibhu Joshi, Jitendra Kumar Shandilya, Dharmagat Bhattarai, Jyoti Sharma, Amit Rawat
Publikováno v:
Genes and Diseases, Vol 7, Iss 1, Pp 84-92 (2020)
Chronic granulomatous disease (CGD) is an inherited defect of phagocyte function due to defective NADPH oxidase. Patients with CGD are not able to effectively clear the infections because of the defect in the phagocyte production of oxygen free radic
Externí odkaz:
https://doaj.org/article/c822bb48d99148d0885de0b562022800
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:
Luigi D. Notarangelo, Anit Kaur, Alejandro C. Briones, Ankita Singh, Anju Gupta, Pandiarajan Vignesh, Francesca Pala, Mandeep Walia, Surjit Singh, Man Updesh Singh Sachdeva, Kerry Dobbs, Deepti Suri, Amit Rawat, Ankur Kumar Jindal, Jitendra Kumar Shandilya, Ottavia M. Delmonte, José R. Regueiro
Publikováno v:
J Clin Immunol
We report a non-consanguineous family from North-west India in which 3 siblings succumbed to a rare variant of combined immunodeficiency. All three had similar clinical and immunological profiles. However, the youngest child also developed Non-Hodgki
Autor:
Jyoti Sharma, Amit Rawat, Dharmagat Bhattarai, Vibhu Joshi, Pandiarajan Vignesh, Gummadi Anjani, Jitendra Kumar Shandilya
Publikováno v:
Genes & Diseases
Genes and Diseases, Vol 7, Iss 1, Pp 84-92 (2020)
Genes and Diseases, Vol 7, Iss 1, Pp 84-92 (2020)
Chronic granulomatous disease (CGD) is an inherited defect of phagocyte function due to defective NADPH oxidase. Patients with CGD are not able to effectively clear the infections because of the defect in the phagocyte production of oxygen free radic
Autor:
Rakesh Kumar Pilania, Deepti Suri, Ashwin Dalal, Surjit Singh, Jitendra Kumar Shandilya, Pandiarajan Vignesh, Anupriya Kaur, Anit Kaur, Asodu Sandeep Sarma, Madhubala Sharma, Shubham Goel, Amit Rawat
Publikováno v:
Journal of Clinical Immunology. 39:611-615
Autor:
Pandiarajan Vignesh, Anju Gupta, Vijai Williams, Amit Rawat, Jitendra Kumar Shandilya, Surjit Singh
Publikováno v:
International Journal of Rheumatic Diseases. 22:449-457
BACKGROUND Polymorphisms in the Fcγ-receptor (FcγR) have been associated with increased susceptibility to systemic lupus erythematosus (SLE). There is a paucity of data on FcγR expression pattern in pediatric subjects with SLE. The aim of the stud
Autor:
Deepak Bansal, Prateek Bhatia, Man Updesh Singh Sachdeva, Minu Singh, Richa Jain, Amit Rawat, Amita Trehan, Siddharth K Totadri, Jitendra Kumar Shandilya, Neelam Varma
Publikováno v:
Asian Pacific Journal of Cancer Prevention : APJCP
Background: Immunophenotypic markers can play significant role in prognostic assessment for different cancers and leukocyte-associated Ig-like receptor (LAIR-1) is a recently identified inhibitory immuno-receptor. Methods: We measured LAIR-1 expressi
Autor:
Jasmina Ahluwalia, Man Updesh Singh Sachdeva, Amit Rawat, Surjit Singh, Jitendra Kumar Shandilya, Pandiarajan Vignesh
Publikováno v:
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-7 (2021)
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-7 (2021)
Background Platelet activation is an integral part of pathogenesis of Kawasaki disease (KD). However, there is paucity of literature on flow-cytometry based assessment of platelet activation in KD. We aimed to analyse monocyte-platelet aggregates (MP