Sharmim, M. S., Begum, A., Hossain, D. and Shanta, S. N. (2025) “Enigmatic response of frequent use of rituximab in multidrug resistant nephrotic syndrome with focal segmental glomerulosclerosis with NPHS1 gene mutation children: genetic and pathophysiological consideration”, International Journal of Contemporary Pediatrics, 12(5), pp. 831–834. doi: 10.18203/2349-3291.ijcp20251106.