Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Shashikant Apte"'
Autor:
Ajay Gandhi, Klaus Görlinger, Sukesh C Nair, Poonam M Kapoor, Anjan Trikha, Yatin Mehta, Anil Handoo, Anil Karlekar, Jyoti Kotwal, Joseph John, Shashikant Apte, Vijay Vohra, Gajendra Gupta, Aseem K Tiwari, Anjali Rani, Shweta A Singh
Publikováno v:
Journal of Anaesthesiology Clinical Pharmacology, Vol 37, Iss 1, Pp 3-13 (2021)
In a developing country like India, with limited resources and access to healthcare facilities, dealing with massive hemorrhage is a major challenge. This challenge gets compounded by pre-existing anemia, hemostatic disorders, and logistic issues of
Externí odkaz:
https://doaj.org/article/8b897e5547504014ae4a66f6cbc8b555
Autor:
Jorge E. Cortes, Tapan Saikia, Dong-Wook Kim, Yesid Alvarado, Franck E. Nicolini, Krishnakumar Rathnam, Navin Khattry, Sachin Punatar, Jane F. Apperley, Aude Charbonnier, Michael Deininger, Hugues de Lavallade, Nikki Granacher, Carlo Gambacorti-Passerini, Alessandro Lucchesi, Michael Mauro, Peter Vandenberghe, Gregor Verhoef, Andrew R. Whiteley, Arijit Nag, Shashikant Apte, Siu-Long Yao, Sandeep Inamdar, Ruchika Irene Dillu, Jayasree Sreenivasan, Geetanjali Chimote
Publikováno v:
Blood. 140:205-207
Publikováno v:
Haemophilia, Vol. 28, no. Suppl 4, p. 93-102 (2022)
New treatment possibilities and modalities are now available globally for patients with haemophilia requiring surgery or invasive procedures. The first is the appropriate application of low-dose protocols of clotting factor concentrates (CFC) achievi
Autor:
S. Chandrakala, Manoj Toshniwal, Mitesh Halvawala, Namita Padwal, Neeraj Sidharthan, Pankaj Malhotra, B. Prashantha, Riya Ballikar, Sandip Shah, Shashikant Apte, T. Kasi Viswanathan, Vijay Ramanan, Akhilesh Sharma, Dattatray Pawar, Roshan Pawar, Vinayaka Shahavi
Publikováno v:
Indian Journal of Hematology and Blood Transfusion.
Publikováno v:
International Journal of Environmental Science and Technology. 19:11935-11962
Plastic pollution is one of the major problems being faced by the world today. The lack of proper recycling and insufficient waste management practices; leaves more than 55% of plastic waste unattended resulting in open dumping of plastic waste. Micr
Autor:
Nirmalkumar Choraria, Savita Rangarajan, M. Joseph John, Shashikant Apte, Pritam Gupta, Seema Pai, Rohit Chand, Shyam Parvatini, G. S. H. Ramakanth, Jeremy Rupon, Amit Chhabra, Hitesh Bhaskarrao Muley, Damien Simoneau
Purpose Hemophilia B is an X-linked congenital bleeding disorder caused by a deficiency of coagulation factor IX (FIX) clotting activity. This study evaluated safety and efficacy of nonacog alfa, a recombinant human blood coagulation FIX replacement
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7380f90c71ed20682cb2abe14460e41
https://eprints.soton.ac.uk/473008/
https://eprints.soton.ac.uk/473008/
Autor:
S. Chandrakala, Manoj Toshniwal, Mitesh Halvawala, Namita Padwal, Neeraj Sidharthan, Pankaj Malhotra, B. Prashantha, Riya Ballikar, Sandip Shah, Shashikant Apte, T. Kasi Viswanathan, Vijay Ramanan, Akhilesh Sharma, Dattatray Pawar, Roshan Pawar, Vinayaka Shahavi
Publikováno v:
Indian Journal of Hematology and Blood Transfusion.
Romiplostim is a Food and Drug Administration (FDA)-approved therapy for immune thrombocytopenia (ITP). Biosimilar is a biological product that has no clinical meaningful difference from an existing FDA-approved reference product. It has a potential
Autor:
Nirmalkumar Choraria, Savita Rangarajan, M. Joseph John, Shashikant Apte, Pritam Gupta, Seema Pai, Rohit Chand, Shyam Parvatini, G. S. H. Ramakanth, Jeremy Rupon, Amit Chhabra, Hitesh Bhaskarrao Muley, Damien Simoneau
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion.
Purpose Hemophilia A is an X-linked congenital disorder, characterized by factor VIII (FVIII) deficiency. Globally, India has the highest population of patients with hemophilia, and there is a clear unmet need for appropriate and effective treatment
Autor:
Chandrakala Shanmukhaiah, Farah Jijina, S Kannan, Nanda G Pai, Bipin Kulkarni, Santosh V Khuba, Madiha Shaikh, Aditi Joshi, Rajesh Phatale, Shashikant Apte
Publikováno v:
Haemophilia : the official journal of the World Federation of HemophiliaREFERENCES. 28(2)
von Willebrand disease (VWD) is the common bleeding disorder with a clinically relevant bleeding prevalence of 1:10,000. von Willebrand disease patients lack both von Willebrand factor (VWF) and factor VIII (FVIII), which are critical for normal haem
Publikováno v:
Haemophilia, Vol. 27, no. Suppl 3, p. 46-52 (2021)
The performance of surgery and invasive procedures in patients with haemophilia is currently facing new challenges globally. The first is the appropriate application of low-dose protocols of clotting factor concentrates (CFC) achieving adequate perio