Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Jasmita Das"'
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 7, Iss 4, Pp S10- (2022)
Externí odkaz:
https://doaj.org/article/eac55519d326442a98c93a73a9c4a6a9
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 2, Pp 55-61 (2024)
Congenital dyserythropoietic anemia (CDA) are a diverse category of heritable anemia. The causative genetic abnormalities interfere with the normal developmental process of erythrocyte maturation inside the bone marrow. As a consequence, red blood ce
Externí odkaz:
https://doaj.org/article/9797929bd085492cb41ce17695bb8b5d
Publikováno v:
Indian J Hematol Blood Transfus
A primary immune deficiency disorder is often suspected in children with recurrent deep seated and fungal infections and those admitted to pediatric intensive care units. Chronic granulomatous disease (CGD) is inherited disorder leading to infections
Autor:
Amiya Ranjan Nayak, Neelabh Nayan, Priyanka Naranje, Pradeep Kumar, Jasmita Dass, Mukul Aggarwal
Publikováno v:
Turkish Journal of Hematology, Vol 41, Iss 3, Pp 205-206 (2024)
Externí odkaz:
https://doaj.org/article/28399ff8b534422ba38fc50679270296
Autor:
Hareram Pandey, Kanwaljeet Singh, Ravi Ranjan, Jasmita Dass, Seema Tyagi, Tulika Seth, Renu Saxena, Manoranjan Mahapatra
Publikováno v:
Journal of Laboratory Physicians, Vol 15, Iss 04, Pp 583-589 (2023)
Introduction Fetal hemoglobin (HbF) levels play significant role in lowering down the morbidity and mortality in sickle cell disease (SCD) patients. Coinheritance of heme oxygenase-1 (HMOX1) rs2071746:A > T polymorphism may contribute to variable HbF
Externí odkaz:
https://doaj.org/article/4ed4ef64e0814337ac78c8886ba6f8d0
Autor:
Amiya Nayak, Pratyusha Gudapati, Swapnil Tripathi, Jasmita Dass, Mukul Aggarwal, Pradeep Kumar
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 16, Iss 1 (2024)
Autoimmune lymphoproliferative syndrome (ALPS) is a disease characterized by dysfunction of the T lymphocyte apoptotic pathways, mostly due to dysfunctional FAS mediated signaling. However few cases can also occur independent of FAS pathway alteratio
Externí odkaz:
https://doaj.org/article/185709511c1a4ecdbbd4f5b11e61ef1d
Publikováno v:
Journal of Laboratory Physicians, Vol 15, Iss 03, Pp 392-398 (2023)
Background Immunophenotyping and enumeration of plasma cells (PCs) by flow cytometry are deemed to be prognostically significant. However, PCs enumeration by flow cytometry is challenging owing to discrepancy with morphology and PCs loss during sampl
Externí odkaz:
https://doaj.org/article/77cd042864444200a2277d005396a3b7
Publikováno v:
Current Medicine Research and Practice. 8:144-146
Autor:
Ganesh Kumar Viswanathan, Jasmita Dass, Rishi Dhawan, Mukul Aggarwal, Pradeep Kumar, Tulika Seth, Manoranjan Mahapatra
Publikováno v:
HemaSphere, Vol 7, p e27456f6 (2023)
Externí odkaz:
https://doaj.org/article/612d24de16e04251aa41847a7a446b3e
Autor:
Priya Thakur, Pragya Gupta, Nupur Bhargava, Rajat Soni, Narendra Varma Gottumukkala, Sangam Giri Goswami, Gaurav Kharya, Vinodh Saravanakumar, Padma Gunda, Suman Jain, Jasmita Dass, Mukul Aggarwal, Sivaprakash Ramalingam
Publikováno v:
Diagnostics, Vol 12, Iss 7, p 1765 (2022)
Sickle cell disease (SCD) is the most prevalent life-threatening blood monogenic disorder. Currently, there is no cure available, apart from bone marrow transplantation. Early and efficient diagnosis of SCD is key to disease management, which would m
Externí odkaz:
https://doaj.org/article/53809a58ee74487d832c6189943ff76d