Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Chander Hans"'
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 138, Iss , Pp 111512- (2021)
Externí odkaz:
https://doaj.org/article/68f92f2b17c9422b8ed4b110a486912e
Autor:
Debadrita Ray, Narender Kumar, Chander Hans, Anita Kler, Richa Jain, Deepak Bansal, Amita Trehan, Arihant Jain, Pankaj Malhotra, Jasmina Ahluwalia
Publikováno v:
Blood Research. 58:61-70
Autor:
Ritika Sharma, Manu Jamwal, Hari Kishan Senee, Namrata Singh, Narender Kumar, Chander Hans, Anita Kler, Deepak Bansal, Amita Trehan, Pankaj Malhotra, Jasmina Ahluwalia, Reena Das
Publikováno v:
Haemophilia. 29:591-599
Inherited Factor VII (FVII) deficiency is commonest among the rare bleeding disorders. A small number of patients present in infancy with severe bleeding, and many may remain asymptomatic but detected before surgery/invasive procedures. Genetic testi
Autor:
Khalid Abdul Mannan, Narender Kumar, Jasmina Ahluwalia, Chander Hans, Anita Kler, Gaurav Prakash, Richa Jain
Publikováno v:
International Journal of Laboratory Hematology. 45:241-249
The clot waveform analysis (CWA) provide valuable information beyond clotting time. The present study was planned to assess whether the activated partial thromboplastin time (aPTT)-CWA can differentiate between hemophilia A (HA), hemophilia B (HB), o
Autor:
Debadrita Ray, Narender Kumar, Chander Hans, Anita Kler, Richa Jain, Deepak Bansal, Amita Trehan, Arihant Jain, Pankaj Malhotra, Jasmina Ahluwalia
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 38:703-709
Factor VIII replacement is the mainstay of treatment in hemophilia A but may lead to the development of inhibitors. While a vexing clinical problem, some observations suggest that the presence of inhibitors may not necessarily portend a higher bleedi
Autor:
Prashant Sharma, Chander Hans, Rahul Saini, MU.S. Sachdeva, AlkaRani Khadwal, ParveenLata Bose, Reena Das
Publikováno v:
Journal of Microscopy and Ultrastructure.
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 138, Iss, Pp 111512-(2021)