Dr Kaustuv Bhattacharya

Lecturer
Paediatrics & Child Health, Children's Hospital, Westmead

Telephone +61 2 9845 3650
Fax 98453121

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Selected publications

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Journals

  • Coman, D., Bhattacharya, K. (2012). Extended newborn screening: An update for the general paediatrician. Journal of Paediatrics and Child Health, 48(2), E68-E72. [More Information]
  • Bhattacharya, K. (2011). Dietary dilemmas in the management of glycogen storage disease type I. Journal of Inherited Metabolic Disease (JIMD), 34(3), 621-629. [More Information]
  • Shanti, B., Silink, M., Bhattacharya, K., Howard, N., Carpenter, K., Fietz, M., Clayton, P., Christodoulou, J. (2009). Congenital disorder of glycosylation type Ia: Heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency. Journal of Inherited Metabolic Disease (JIMD), Short Report #166 - online, 1-11. [More Information]
  • Bhattacharya, K., Khalili, V., Wiley, V., Carpenter, K., Wilcken, B. (2006). Newborn screening may fail to identify intermediate forms of maple syrup urine disease. Journal of Inherited Metabolic Disease (JIMD), 29(4), 586-586. [More Information]

2012

  • Coman, D., Bhattacharya, K. (2012). Extended newborn screening: An update for the general paediatrician. Journal of Paediatrics and Child Health, 48(2), E68-E72. [More Information]

2011

  • Bhattacharya, K. (2011). Dietary dilemmas in the management of glycogen storage disease type I. Journal of Inherited Metabolic Disease (JIMD), 34(3), 621-629. [More Information]

2009

  • Shanti, B., Silink, M., Bhattacharya, K., Howard, N., Carpenter, K., Fietz, M., Clayton, P., Christodoulou, J. (2009). Congenital disorder of glycosylation type Ia: Heterogeneity in the clinical presentation from multivisceral failure to hyperinsulinaemic hypoglycaemia as leading symptoms in three infants with phosphomannomutase deficiency. Journal of Inherited Metabolic Disease (JIMD), Short Report #166 - online, 1-11. [More Information]

2006

  • Bhattacharya, K., Khalili, V., Wiley, V., Carpenter, K., Wilcken, B. (2006). Newborn screening may fail to identify intermediate forms of maple syrup urine disease. Journal of Inherited Metabolic Disease (JIMD), 29(4), 586-586. [More Information]

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