Archana M VManipal Academy of Higher Education | MAHE · Pediatric Hematology and oncology
Archana M V
Bachelor of Medicine
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Citations since 2017
23 Research Items
Introduction: L‑Asparaginase is an essential chemotherapeutic agent in the therapy of Acute Lymphoblastic Leukemia (ALL), which has led to improvement in survival. In low and middle-income countries like India, the outcomes in ALL are inferior compared to the published literature, one of the cause of which are believed to be due to the inferior qua...
Introduction Hemoglobinopathies are inherited disorders of red blood cells that poses significant cause of morbidity and mortality, impose a heavy burden on family. The study aims to assess the awareness of Thalassemia, and its willingness to screen among young women from Udupi district. Methods A descriptive cross-sectional survey design was empl...
Introduction Renal infiltration by leukemia causing massive bilateral nephromegaly is an extremely rare presentation of T-cell acute lymphoblastic leukemia(T-ALL). Case report 18-month-old female toddler presented with fever and progressive abdominal distension of 4-6 weeks duration. Imaging revealed bilateral massively enlarged kidneys with norma...
BACKGROUND: Outcomes in childhood cancer has dramatically improved in the West due to intensification of chemotherapy along with improved supportive care, however in LMIC like ours, deaths in remission secondary to MDR sepsis and viral infections is alarming and has drastically reduced cure rates. Very few IV antibiotics have been FDA approved late...
Background and Aims: Outcomes in childhood cancer has dramatically improved in the west due to intensification of chemotherapy and improved supportive care. In LMIC like India, infections related deaths brings down the overall childhood cancer outcome. Also, there is an alarming rise in MDR infections among pediatric cancer patients in India and th...
Primary immunodeficiencies (PIDs) are a rare and heterogeneous group of inherited genetic disorders that are characterized by an absent or impaired immune system. In this report, we describe the use of next-generation sequencing to investigate a male infant with clinical and immunological manifestations suggestive of a PID. Whole-exome sequencing o...