Vrushali Satish Takalikar
2PUBLICATIONS
1CO-AUTHORS
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Publications (2)
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|Feb 27, 2024
Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by TRPM6 gene mutation.Savita Khadse, Vrushali Satish Takalikar, Radha Ghildiyal
|Sep 12, 2023
Rare cause of persistent hypocalcaemia in infancy due to PTH gene mutation.Savita Khadse, Vrushali Satish Takalikar, Radha Ghildiyal
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