Vrushali Satish Takalikar

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 5

Top Topics

Intellectual Disability

Blood Brain Barrier

Top Venues

BMJ case reports

This page only lists publications with an associated author ORCID identifier.

Publications

Savita Khadse, Vrushali Satish Takalikar, Radha Ghildiyal, Karishma Bhade
Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by TRPM6 gene mutation. BMJ case reports 17 (2) (2024)
Savita Khadse, Vrushali Satish Takalikar, Radha Ghildiyal, Karishma Bhade
Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by TRPM6 gene mutation. BMJ case reports 17 (2) (2024)
Savita Khadse, Vrushali Satish Takalikar, Radha Ghildiyal, Karishma Bhade
Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by TRPM6 gene mutation. BMJ case reports 17 (2) (2024)
Savita Khadse, Vrushali Satish Takalikar, Radha Ghildiyal, Karishma Bhade
Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by TRPM6 gene mutation. BMJ case reports 17 (2) (2024)
Savita Khadse, Vrushali Satish Takalikar, Radha Ghildiyal, Nikhil Shah
Rare cause of persistent hypocalcaemia in infancy due to PTH gene mutation. BMJ case reports 16 (9) (2023)