Zobrazeno 1 - 10
of 143
pro vyhledávání: '"Fouzia Na"'
Autor:
Pai AA, Mohan A, Benjamin ESB, Illangeswaran RSS, Xavier Raj I, Janet NB, Arunachalam AK, Kavitha ML, Kulkarni U, Devasia AJ, Fouzia NA, Abraham A, Srivastava A, George B, Mathews V, Korula A, Balasubramanian P
Publikováno v:
Pharmacogenomics and Personalized Medicine, Vol Volume 14, Pp 1303-1313 (2021)
Aswin Anand Pai, Ajith Mohan, Esther Sathya Bama Benjamin, Raveen Stephen Stallon Illangeswaran, Infencia Xavier Raj, Nancy Beryl Janet, Arun Kumar Arunachalam, ML Kavitha, Uday Kulkarni, Anup J Devasia, NA Fouzia, Aby Abraham, Alok Srivastava, Biju
Externí odkaz:
https://doaj.org/article/b0ffbc1821a4463c8141e747297ddb08
Autor:
Balaji Balakrishnan, Raveen Stephen Stallon Illangeswaran, Bharathi M Rajamani, Aswin Anand Pai, Infencia Xavier Raj, Daniel Zechariah Paul, Kavitha Lakshmi, Thenmozhi Mani, Ezhilpavai Mohanan, Uday Kulkarni, Anup Joseph Devasia, Fouzia NA, Anu Korula, Aby Abraham, Alok Srivastava, Vikram Mathews, Sophie Paczesny, Biju George, Poonkuzhali Balasubramanian
Publikováno v:
eJHaem, Vol 1, Iss 1, Pp 219-229 (2020)
Abstract Early complications post hematopoietic stem cell transplantation (HSCT) such as sinusoidal obstruction syndrome (SOS) and graft versus host disease (GVHD) can be life threatening. Although several biomarkers have been identified to correlate
Externí odkaz:
https://doaj.org/article/22f625e9d97d4f0298a2106c70e13e93
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:
Devasia, Anup J *, Abraham, Melvin Alex, Sagadevan, Chidambaram, Korula, Anu, Kulkarni, Uday, Fouzia, NA, Abraham, Aby, Srivastava, Alok, Mathews, Vikram, George, Sajan Philip, George, Biju
Publikováno v:
In Transfusion and Apheresis Science February 2021 60(1)
Autor:
Manju Sengar, Anu Korula, Prasanth Ganesan, Akhil Rajendra, Hasmukh Jain, Prasanna Samuel, Jayachandran P K, Gaurav Prakash, M. Joseph John, Rasmi Palassery, Chandran K. Nair, Tanuja Shet, Sushil Selvarajan, Lingaraj Nayak, Parathan Karunakaran, Fouzia NA, Om Prakash, Bhausaheb Bagal, Nikita Mehra, Saranya Kumaran, Sridhar Epari, Jayshree Thorat, Venkatraman Radhakrishnan, Aby Abraham
Publikováno v:
Blood. 140:6687-6689
Autor:
Ajith Mohan, Nancy Beryl Janet, Poonkuzhali Balasubramanian, Uday Kulkarni, Fouzia Na, M. L. Kavitha, Raveen Stephen Stallon Illangeswaran, Infencia Xavier Raj, Aby Abraham, Esther Sathya Bama Benjamin, Biju George, Anup J. Devasia, Vikram Mathews, Arun Kumar Arunachalam, Aswin Anand Pai, Alok Srivastava, Anu Korula
Publikováno v:
Pharmacogenomics and Personalized Medicine
Aswin Anand Pai, Ajith Mohan, Esther Sathya Bama Benjamin, Raveen Stephen Stallon Illangeswaran, Infencia Xavier Raj, Nancy Beryl Janet, Arun Kumar Arunachalam, ML Kavitha, Uday Kulkarni, Anup J Devasia, NA Fouzia, Aby Abraham, Alok Srivastava, Biju
Autor:
Aswin Anand Pai, K B Nayanthara, Uday Kulkarni, Kavitha Lakshmi, Raveen Stephen Stallon Illangeswaran, Ezhilpavai Mohanan, J Agila, Anu Korula, Fouzia NA, Anup J Devasia, Sharon Lionel, Sushil Selvarajan, Eunice Sindhuvi, Aby Abraham, Alok Srivastava, Biju George, Vikram Mathews, Poonkuzhali Balasubramanian
Publikováno v:
Transplantation and Cellular Therapy. 29:S160-S161
Comprehensive laboratory diagnosis of Fanconi anaemia: comparison of cellular and molecular analysis
Autor:
Gaurav Joshi, Nancy Beryl Janet Arthur, Thenral S Geetha, Phaneendra Venkateswara Rao Datari, Kirti Modak, Debanjan Roy, Anurag Dutta Chaudhury, Prasanth Sundaraganesan, Sweety Priyanka, Fouzia NA, Vedam Ramprasad, Aby Abraham, Vivi M Srivastava, Alok Srivastava, Uday Prakash Kulkarni, Biju George, Shaji R Velayudhan
Publikováno v:
Journal of Medical Genetics. :jmedgenet-2022
BackgroundFanconi anaemia (FA) is a rare inherited bone marrow failure disease caused by germline pathogenic variants in any of the 22 genes involved in the FA-DNA interstrand crosslink (ICL) repair pathway. Accurate laboratory investigations are req
Autor:
Uday Prakash Kulkarni, Sushil Selvarajan, Fouzia NA, Sharon Lionel, Sukesh C Nair, Poonkuzhali Balasubramanian, Thenmozhi Mani, Aby Abraham, Biju George, Vikram Mathews
Publikováno v:
Blood. 140:8917-8918