Dr Kaustuv Bhattacharya

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

Telephone +61 2 9845 3650
Fax 98453121

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Clinical Specialty

Paediatrics

Selected publications

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Journals

  • Montano, A., Lock-Hock, N., Steiner, R., Graham, B., Szlago, M., Greenstein, R., Pineda, M., Gonzalez-Meneses, A., Coker, M., Bhattacharya, K., et al (2016). Clinical course of sly syndrome (mucopolysaccharidosis type VII). Journal of Medical Genetics, 53(6), 403-418. [More Information]
  • Menezes, M., Rahman, S., Bhattacharya, K., Clark, D., Christodoulou, J., Ellaway, C., Farrar, M., Pitt, M., Sampaio, H., Ware, T., Ouvrier, R., et al (2016). Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease. Mitochondrion, 30, 162-167. [More Information]
  • Bhattacharya, K., Mundy, H., Lilburn, M., Champion, M., Morley, D., Maillot, F. (2015). A pilot longitudinal study of the use of waxy maize heat modified starch in the treatment of adults with glycogen storage disease type I: A randomized double-blind cross-over study. Orphanet Journal of Rare Diseases, 10(1), 1-11. [More Information]
  • Berrier, K., Kazi, Z., Prater, S., Bali, D., Goldstein, J., Stefanescu, M., Rehder, C., Botha, E., Ellaway, C., Bhattacharya, K., et al (2015). CRIM-negative infantile Pompe disease: characterization of immune responses in patients treated with ERT monotherapy. Genetics in Medicine, 17(11), 912-918. [More Information]
  • Choy, Y., Bhattacharya, K., Balasubramaniam, S., Fietz, M., Fu, A., Inwood, A., Jin, D., Kim, O., Kosuga, M., Kwun, Y., et al (2015). Identifying the need for a multidisciplinary approach for early recognition of mucopolysaccharidosis VI (MPS VI). Molecular Genetics and Metabolism, 115(1), 41-47. [More Information]
  • Bhattacharya, K. (2015). Investigation and management of the hepatic glycogen storage diseases. Translational Pediatrics, 4(3), 240-248.
  • Bhattacharya, K. (2015). Where will genetic research take us? Translational Pediatrics, 4(4), 318-319. [More Information]
  • Estrella, J., Wilcken, B., Carpenter, K., Bhattacharya, K., Tchan, M., Wiley, V. (2014). Expanded newborn screening in New South Wales: missed cases. Journal of Inherited Metabolic Disease (JIMD), 37(6), 881-887. [More Information]
  • Ho, G., Alexander, I., Bhattacharya, K., Dennison, B., Ellaway, C., Thompson, S., Wilcken, B., Christodoulou, J. (2014). The Molecular Bases of Phenylketonuria (PKU) in New South Wales, Australia: Mutation Profile and Correlation with Tetrahydrobiopterin (BH4) Responsiveness. JIMD Reports, 14, 55-65. [More Information]
  • Baker, P., Friederich, M., Swanson, M., Shaikh, T., Bhattacharya, K., Scharer, G., Aicher, J., Creadon-Swindell, G., Geiger, E., Maclean, K., Procopis, P., et al (2014). Variant non-ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5. Brain, 137(2), 366-379. [More Information]
  • 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]
  • Dagli, A., Lee, P., Correia, C., Rodriguez, C., Bhattacharya, K., Steinkrauss, L., Stanley, C., Weinstein, D. (2010). Pregnancy in glycogen storage disease type Ib: gestational care and report of first successful deliveries. Journal of Inherited Metabolic Disease (JIMD), 33(Suppl 3), S151-S157. [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]

2016

  • Montano, A., Lock-Hock, N., Steiner, R., Graham, B., Szlago, M., Greenstein, R., Pineda, M., Gonzalez-Meneses, A., Coker, M., Bhattacharya, K., et al (2016). Clinical course of sly syndrome (mucopolysaccharidosis type VII). Journal of Medical Genetics, 53(6), 403-418. [More Information]
  • Menezes, M., Rahman, S., Bhattacharya, K., Clark, D., Christodoulou, J., Ellaway, C., Farrar, M., Pitt, M., Sampaio, H., Ware, T., Ouvrier, R., et al (2016). Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease. Mitochondrion, 30, 162-167. [More Information]

2015

  • Bhattacharya, K., Mundy, H., Lilburn, M., Champion, M., Morley, D., Maillot, F. (2015). A pilot longitudinal study of the use of waxy maize heat modified starch in the treatment of adults with glycogen storage disease type I: A randomized double-blind cross-over study. Orphanet Journal of Rare Diseases, 10(1), 1-11. [More Information]
  • Berrier, K., Kazi, Z., Prater, S., Bali, D., Goldstein, J., Stefanescu, M., Rehder, C., Botha, E., Ellaway, C., Bhattacharya, K., et al (2015). CRIM-negative infantile Pompe disease: characterization of immune responses in patients treated with ERT monotherapy. Genetics in Medicine, 17(11), 912-918. [More Information]
  • Choy, Y., Bhattacharya, K., Balasubramaniam, S., Fietz, M., Fu, A., Inwood, A., Jin, D., Kim, O., Kosuga, M., Kwun, Y., et al (2015). Identifying the need for a multidisciplinary approach for early recognition of mucopolysaccharidosis VI (MPS VI). Molecular Genetics and Metabolism, 115(1), 41-47. [More Information]
  • Bhattacharya, K. (2015). Investigation and management of the hepatic glycogen storage diseases. Translational Pediatrics, 4(3), 240-248.
  • Bhattacharya, K. (2015). Where will genetic research take us? Translational Pediatrics, 4(4), 318-319. [More Information]

2014

  • Estrella, J., Wilcken, B., Carpenter, K., Bhattacharya, K., Tchan, M., Wiley, V. (2014). Expanded newborn screening in New South Wales: missed cases. Journal of Inherited Metabolic Disease (JIMD), 37(6), 881-887. [More Information]
  • Ho, G., Alexander, I., Bhattacharya, K., Dennison, B., Ellaway, C., Thompson, S., Wilcken, B., Christodoulou, J. (2014). The Molecular Bases of Phenylketonuria (PKU) in New South Wales, Australia: Mutation Profile and Correlation with Tetrahydrobiopterin (BH4) Responsiveness. JIMD Reports, 14, 55-65. [More Information]
  • Baker, P., Friederich, M., Swanson, M., Shaikh, T., Bhattacharya, K., Scharer, G., Aicher, J., Creadon-Swindell, G., Geiger, E., Maclean, K., Procopis, P., et al (2014). Variant non-ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5. Brain, 137(2), 366-379. [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]

2010

  • Dagli, A., Lee, P., Correia, C., Rodriguez, C., Bhattacharya, K., Steinkrauss, L., Stanley, C., Weinstein, D. (2010). Pregnancy in glycogen storage disease type Ib: gestational care and report of first successful deliveries. Journal of Inherited Metabolic Disease (JIMD), 33(Suppl 3), S151-S157. [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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