Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Vibha Bafna"'
Autor:
Revathi Raj, Ramya Uppuluri, Badira Parambil, Nidhi Dhariwal, Sidharth Totadri, Leni Grace Mathew, Venkatraman Radhakrishnan, Abhishek Charan, Satya Prakash Yadav, Amita Mahajan, Sangeeta Mudaliar, Ratna Sharma, Mamta Manglani, Gaurav Kharya, Nishant Verma, Ramandeep Arora, Niharendu Ghara, Reghu KS, Nita Radhakrishnan, Nisha Iyer, Priti Mehta, Amitabh Singh, Shivani Patel, Joseph John, Sunil Bhat, Shobha Badiger, Sirisharani Siddaiahgari, Shruti Kakkar, Julius Scott, Dhaarani Jayaraman, Arathi Srinivasan, Yamini Krishnan, Ngangbam Sonamani, Ruchira Misra, Vibha Bafna, Rachna Seth, Purvi Kadakia Kutty, Swati Kanakia, Vasudha Rao, Anand Prakash, Vandana Bharadwaj, Girish Chinnasamy
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 2, Pp 34-37 (2022)
Introduction: The clinical outcomes of COVID-19 infection in children with cancer have been variable worldwide. Therefore, we aimed to collect data from all regions in India through a national collaborative study and identify factors that cause morta
Externí odkaz:
https://doaj.org/article/64c0edec81544be1a782a0b2b399959f
Autor:
Reema Garegrat, Suprabha K Patnaik, Nandini Malshe, Sandip P Bartakke, Vibha Bafna, Pradeep Suryawanshi
Publikováno v:
Indian Pediatrics Case Reports, Vol 2, Iss 2, Pp 102-106 (2022)
Background: Clinical, pathologic, and genetic heterogeneity is a challenge in identifying and classifying congenital dyserythropoietic anemia (CDA). CDA type IV, the rarest CDA with only 11 reported cases, results from KLF1 gene mutation. Clinical De
Externí odkaz:
https://doaj.org/article/82cc355ccee442459f9b69f5fb26bf42
Autor:
Manjusha Sajith, Atmaram Pawar, Abdulrahaman A. Momin, Vibha Bafna, Sandeep Bartakke, Kannan Subramaniyan
Publikováno v:
Journal of Krishna Institute of Medical Sciences University, Vol 09, Iss 03, Pp 27-39 (2020)
Background: Methotrexate (MTX) blocks Methylene Tetrahydrofolate Reductase (MTHFR) Enzyme thereby, interrupt folate metabolism, it is used in the treatment of cancer and autoimmune disorders. Aim and Objectives: The present study aimed to evaluat
Externí odkaz:
https://doaj.org/article/3a3cdf1a82c54ee1b85deb704faaf43e
Publikováno v:
Indian Journal of Rheumatology, Vol 15, Iss 3, Pp 223-225 (2020)
Chronic granulomatous disease (CGD) is an inherited neutrophil phagocytic function disorder leading to recurrent infections, granuloma formations, and rarely autoimmune diseases. We report a case of genetically proven autosomal recessive CGD in a chi
Externí odkaz:
https://doaj.org/article/47dd71ed1d4848c5b7eef2498988388a
Autor:
Putun Patel, Sandip Bartakke, Vibha Bafna, Bhakti Sarangi, Kavita Srivastava, Jitendra Oswal, Vijay Kalrao, Sanjay Lalwani
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 2, p S21 (2017)
Externí odkaz:
https://doaj.org/article/1c178fea8c9346ec8341588fd8e70326
Autor:
Putun Patel, Vibha Bafna, Sandip Bartakke, Dasmeet Singh, Rahul Jahagirdar, Jitendra Oswal, Vijay Kalrao, Sanjay Lalwani
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 2, p S25 (2017)
Externí odkaz:
https://doaj.org/article/080708a769ff4ab182ee8bf691aba6c7
Autor:
Putun Patel, Vibha Bafna, Sandip Bartakke, Priya Gupta, Sanjay Mankar, Jitendra Oswal, Vijay Kalrao, Sanjay Lalwani
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 2, Pp S19-S20 (2017)
Externí odkaz:
https://doaj.org/article/9517900707c54ffabeec1923c120e77a
Autor:
Putun Patel, Sandip Bartakke, Vibha Bafna, Bhakti Sarangi, Jitendra Oswal, Vijay Kalrao, Sanjay Lalwani
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 2, Pp S11-S12 (2017)
Externí odkaz:
https://doaj.org/article/85911a3875d04c6d8fe7d1b38ebf0a71
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 2, Iss 2, p S29 (2017)
Externí odkaz:
https://doaj.org/article/49ef996f43224ef2b56350d82dd4ccb2
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 1, Iss 2, p S3 (2016)
Externí odkaz:
https://doaj.org/article/aa073d5d921a426da7661168ae93653d