Karishma Bhade (Nikhil Shah)

Publication Activity (10 Years)

Years Active: 2024-2024
Publications (10 Years): 9

Top Topics

Top Venues

BMJ case reports

Indian journal of pediatrics

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, Karishma Bhade, Karishma Bhade, Radha Ghildiyal
Follow up of a rare case of adrenal insufficiency due to NNT 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, Karishma Bhade, Karishma Bhade, Radha Ghildiyal
Follow up of a rare case of adrenal insufficiency due to NNT mutation. BMJ case reports 17 (2) (2024)
Anuradha V Khadilkar, Karishma Bhade
Rising Type 2 Diabetes Mellitus in Indian Adolescents: Insights Into Prevalence, Prevention and Predictors. Indian journal of pediatrics (2024)
Savita Khadse, Karishma Bhade, Karishma Bhade, Radha Ghildiyal
Follow up of a rare case of adrenal insufficiency due to NNT mutation. BMJ case reports 17 (2) (2024)
Savita Khadse, Karishma Bhade, Karishma Bhade, Radha Ghildiyal
Follow up of a rare case of adrenal insufficiency due to NNT 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)