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Fatal familial hemophagocytic lymphohistiocytosis with perforin gene (PRF1) mutation and EBV-associated T-cell lymphoproliferative disorder of the thyroid.
Mian A, Kumari K, Kaushal S, Fazal F, Kodan P, Batra A, Kumar P, Baitha U, Jorwal P, Soneja M, Sharma MC, Biswas A. Mian A, et al. Among authors: kumari k. Autops Case Rep. 2019 Jul 19;9(3):e2019101. doi: 10.4322/acr.2019.101. eCollection 2019 Jul-Sep. Autops Case Rep. 2019. PMID: 31440481 Free PMC article.
Multiple Neurologic Deficits and Cognitive Decline in a Young Woman.
Elavarasi A, George J, Sharma MC, Kumari K, Garg A, Pandit AK, Satapathy A, Goyal V. Elavarasi A, et al. Among authors: kumari k. Ann Indian Acad Neurol. 2019 Oct-Dec;22(4):506-512. doi: 10.4103/aian.AIAN_293_19. Epub 2019 Oct 25. Ann Indian Acad Neurol. 2019. PMID: 31736585 Free PMC article.
mTOR pathway activation in focal cortical dysplasia.
Kumari K, Sharma MC, Kakkar A, Malgulwar PB, Pathak P, Suri V, Sarkar C, Chandra SP, Faruq M. Kumari K, et al. Ann Diagn Pathol. 2020 Jun;46:151523. doi: 10.1016/j.anndiagpath.2020.151523. Epub 2020 Apr 10. Ann Diagn Pathol. 2020. PMID: 32325422
631 results