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Journal of Paediatrics and Child Health|October 25, 2011
Extended newborn screening: an update for the general paediatricianDavid Coman, Kaustuv BhattacharyaJournal of Inherited Metabolic Disease|April 15, 2011
Dietary dilemmas in the management of glycogen storage disease type IKaustuv BhattacharyaTranslational Pediatrics|February 3, 2016
Investigation and management of the hepatic glycogen storage diseasesKaustuv BhattacharyaJIMD Reports|November 7, 2022
3-Methylglutaconyl-CoA hydratase deficiency: When ascertainment bias confounds a biochemical diagnosisAshley Hertzog, Arthavan Selvanathan, Dinusha Pandithan, et al.Translational Pediatrics|February 3, 2016
The evolution of blood-spot newborn screeningKaustuv Bhattacharya, Tiffany Wotton, Veronica WileyJIMD Reports|June 24, 2016
Rare Case of Hepatic Gaucheroma in a Child on Enzyme Replacement TherapySophy Korula, Penny Owens, Amanda Charlton, et al.Future Oncology (London, England)|February 7, 2022
Financial toxicity and its impact on health outcomes and caregiver burden among adult cancer survivors in the USASushmitha Inguva, Masoom Priyadarshini, Ruchit Shah, et al.Journal of Inherited Metabolic Disease|June 23, 2023
Exercise testing and prescription in patients with inborn errors of muscle energy metabolismKiera Batten, Kaustuv Bhattacharya, David Simar, et al.Journal of Paediatrics and Child Health|April 16, 2021
Rare diseases research and policy in Australia: On the journey to equitable careKaustuv Bhattacharya, Nicole Millis, Adam Jaffe, et al.Journal of Paediatrics and Child Health|June 12, 2018
Infantile-onset Pompe disease: A case series highlighting early clinical features, spectrum of disease severity and treatment responsePenny Owens, Melanie Wong, Kaustuv Bhattacharya, et al.Pageof 15