Radha G. Ghildiyal
Mumbai, MH, India
Last Updated: 09/26/2026
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Found 20 publications
Tuberculosis presenting as an anterior chest wall swelling: three cases.
Journal: Paediatrics and international child health
Published: January 20, 2026
Recessive TMEM167A variants cause neonatal diabetes, microcephaly, and epilepsy syndrome.
Journal: The Journal of clinical investigation
Published: May 21, 2025
Epidemiology and outcome of pediatric acute kidney injury-multicenter observational study from a low-middle-income country.
Journal: Pediatric nephrology (Berlin, Germany)
Published: April 06, 2025
Respiratory insufficiency as a rare presentation in a child with vitamin D-dependent rickets type 1.
Respiratory insufficiency as a rare presentation in a child with vitamin D-dependent rickets type 1.
Journal: BMJ case reports
Published: January 08, 2025
A non-lethal presentation of osteogenesis imperfecta type VIII due to homozygous mutation in P3H1 gene.
Journal: BMJ case reports
Published: October 25, 2024
Rare cause of recurrent hypocalcaemia and functional hypoparathyroidism due to hypomagnesaemia caused by TRPM6 gene mutation.
Journal: BMJ case reports
Published: February 27, 2024
Follow up of a rare case of adrenal insufficiency due to NNT mutation.
Journal: BMJ case reports
Published: February 17, 2024
Rare cause of persistent hypocalcaemia in infancy due to PTH gene mutation.
Journal: BMJ case reports
Published: September 12, 2023
MOYAMOYA disease in an adolescent with HIV-1.
Journal: Oxford medical case reports
Published: April 06, 2023
Early detection of glomerular dysfunction and renal tubulopathy in children with sickle cell disease in India.
Journal: Journal of tropical pediatrics
Published: April 02, 2023
Last Updated: 09/26/2026